Pay It Forward Flashcards

1
Q

Most often injured artery especially at sites of fixation

A

Internal carotid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Refers to increase in blood volume

A

Hyperemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Refers to increase in tissue fluid

A

Cerebral edema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Often the only reliable evidence of the site of impact

A

Scalp soft-tissue swelling

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Most common manifestation of scalp injury

A

Subgaleal hematoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Most commonly caused by fracture of the thin medial orbital wall

A

Orbital emphysema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Most common isolated maxillary fracture

A

Fracture of the maxillary alveolus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Most common isolated sinus fracture

A

Anterolateral wall of the maxillary antrum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Most common form of primary brainstem injury

A

Diffuse axonal injury (DAI)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Most common skeletal injury in child abuse

A

Long bone fractures

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Most commonly recognized intracranial complication from child abuse

A

Subdural hematomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Most common intra-axial manifestation of head injury related to child abuse

A

Diffuse brain swelling

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Views requested in facial trauma

A

Cadwell, Waters, Cross table lateral and Submentovertex / Submental vertex view

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Most common type of fracture of orbits due to trauma

A

Blowout fracture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Most common type of blow out fracture

A

Inferior blowout fracture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Le fort fracture that is described as “floating palate”

A

Le Fort 1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Le Fort fracture described as “pyramidal”

A

Le fort 2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Le Fort fracture described as “craniofacial dysfunction”

A

Le Fort 3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Le Fort fracture described as “dish face deformity”

A

Le Fort 2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Simple mandibular fractures are most commonly found in the

A

Ramus and condyle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

This type of mandibular fracture exhibits cortical ring sign, which is a well coordinated density above the condylar neck on lateral view

A

Subcondylar fractures

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

The most common site of isolated injury to the mandible

A

Mandibular angle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Most malignant grade of astrocytoma

A

Grade IV

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Most malignant form of astrocytoma

A

Glioblastoma multiforme

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Most common type of glioma

A

Glioblastoma multiforme

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Most common hemorrhagic neoplasms in the brain

A

GBM, Metastasis, Oligodendroglioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Ring enhancing lesions on contrast
“MAGIC-DR”

A

First three (3) are MOST COMMON
M - Metastasis
A - Abscess
G - Glioma
I - Infarct (Subacute phase)
C - Contusion
D - Demyelinating disease
R - Radiation Necrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

Calcified Glial Tumors
“Old A.G.E”

A

Old = Oligodendroglioma
A = Astrocytoma
G = GBM
E = Ependymoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

Most common tumor seen in patients with chronic temporal lobe epilepsy

A

Ganglioglioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

Most common location of ganglioglioma

A

Temporal lobe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

Known as the ghost tumor. This intra axial tumor is exquisitely sensitive to steroid and radiotherapy initially, only to rebound with a vengeance

A

Primary CNS lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

This tumor is composed of small blue cells with a high nucleus to cytoplasm ratio packed tightly together in the perivascular spaces

A

Primary CNS lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

Most common tumor associated with medically refractory partial complex seizures

A

Dysembryoplastic neuroepithelial tumor (DNET)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

Most common site for intracranial neoplasms in the pediatric population

A

Posterior fossa, Cerebellum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
35
Q

Most common primary cerebellar neoplasm in the adult population

A

Hemangioblastoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
36
Q

Most common pediatric CNS malignancy (High Grade, Grade IV)

A

Medulloblastoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
37
Q

Most common pediatric posterior fossa tumor

A

Pilocytic astrocytoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
38
Q

Most common site of metastasis of Medulloblastoma

A

Bone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
39
Q

Most common pediatric CNS tumor (Low Grade, Grade I)

A

Pilocytic Astrocytoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
40
Q

Most common location of Pilocytic Astrocytoma

A

Cerebellum (60%)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
41
Q

Most common tumor seen in NF-1

A

Pilocytic Astrocytoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
42
Q

Most common extra-axial neoplasm of adults

A

Meningioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
43
Q

Most common location of meningioma

A

Parasagittal or convexity locations (50%)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
44
Q

Most common location of meningioma in children

A

Ventricles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
45
Q

Most common location of meningioma in the spine

A

Thoracic spine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
46
Q

MRI Imaging findings to determine extra-axial nature of a tumor

A
  1. Prominent pial blood vessel flow voids (80%)
  2. CSF clefts around the tumor margins
  3. Broad dural base (KEY IMAGING FEATURE)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
47
Q

Most common primary vascular supply of meningioma

A

Middle Meningeal Artery, from the external carotid circulation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
48
Q

How many types of meningioma have been discovered by the WHO and how many are classified under each grade?

A

Total of 15 types
9 are Grade I
3 are Grade II
3 are Grade III

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
49
Q

Most common form/transmission of metastasis of extra-axial tumors

A

Dural metastasis

Subdural lesions = hematogenous
Spinal lesions = via Batson’s venous plexuses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
50
Q

This extra axial tumor was previously considered “angioblastic meningioma”. Arises from modified pericapillary smooth muscle cells (pericytes of Zimmerman). Similar imaging to meningioma BUT has a narrow base attachment and is multilobulated (Instead of BROAD dural base and hemispheric)

A

Hemangiopericytoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
51
Q

Ependymomas are most commonly found in

A

Fourth ventricle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
52
Q

Most common extra-axial mass in an adult

A

Meningioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
53
Q

Most common primary tumors to spread to the ventricle where the choroid plexus is the most highly vascular part of the ventricular system

A

Lung carcinoma, RCC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
54
Q

An intraventricular tumor of neuroepithelial lineage arising from the septum pellucidum or the ventricular wall. Has numerous areas of cystic change giving the mass a “swiss cheese” morphology. Hyperintense on both t1 and t2

A

Central neurocytoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
55
Q

An intraventricular tumor rising from the ependymal lining of the ventricular system in the sub ependymal layer. Hypointensity on t1 hyperintensity on t2

A

Subependymoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
56
Q

An intraventricular tumor discovered in the region of the foramen of monro with strong association to tuberous sclerosis. Iso to slightly hyperintense on t1 and hyperintense on t2

A

Subependymal giant cell astrocytoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
57
Q

Phenomenon associated with colloid cyst. Tilting of the head forward will reproduce acute severe headache

A

Brun phenomenon (Colloid cyst)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
58
Q

This lesion is not a true intraventricular neoplasm. Mimics a neoplasm. Characteristically occurs in the anterior superior portion of the third ventricle near the foramen of Monro. Presents with acute onset of severe headache

A

Colloid cyst

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
59
Q

Most common type of neoplasms of the pineal gland

A

Giant cell tumors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
60
Q

Most common intracranial germ cell tumor

A

Germinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
61
Q

Most common sellar masses

A

Pituitary adenoma/s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
62
Q

Pituitary adenoma <10mm in size

A

Microadenoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
63
Q

Pituitary adenoma
>10mm in size

A

Pituitary Macroadenoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
64
Q

Most common of the secreting adenomas and presents with amenorrhea, galactorrhea, or impotence

A

Prolactinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
65
Q

Most common suprasellar mass in the pediatric population

A

Craniopharyngioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
66
Q

TORCH Infections

A

T = Toxoplasmosis
O = Others ( Syphilis, Varicella)
R = Rubella
C = CMV
H = Herpes simplex, HIV

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
67
Q

Most common cause of congenital CNS infection

A

Cytomegalovirus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
68
Q

Frontal sinusitis in children complicated by osteomyelitis with subperiosteal, epidural, and subdural abscesses

A

Pot puffy tumor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
69
Q

Congenital infection with primarily periventricular pattern of injury and dystrophic calcifications. Patients have hepatosplenomegaly, jaundice, chorioretinitis, deafness and cerebral involvement.

A

Cytomegalovirus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
70
Q

Congenital infection with scattered dystrophic calcifications in the white matter, basal ganglia and cortex. Necrotizing encephalitis of the fetal brain occurs. Patients present with microcephaly, chorioretinitis, and mental retardation.

A

Toxoplasmosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
71
Q

Congenital infection associated with diffuse encephalitis with infarction presenting on cranial ultrasound as diffuse brain swelling and patchy areas of hypodensity in the white matter and cortex, with relative sparing of the basal ganglia, thalamus and posterior fossa structures. CSF analysis revealed pleocytosis (increased cell count), increased protein and decreased glucose.

A

Herpes simplex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
72
Q

Most common form of CNS tuberculosis

A

Tuberculous meningitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
73
Q

Most common opportunistic FUNGAL CNS infections

A
  • Cryptococcus
  • Aspergillosis
  • Candidiasis
  • Mucormycosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
74
Q

Most frequently reported CNS fungal infection

A

Cryptococcosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
75
Q

Most common cause of sporadic encephalitis

A

Herpes simplex encephalitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
76
Q

Most common opportunistic CNS infection

A

Toxoplasmosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
77
Q

Most common fungal infection in hiv-positive patients

A

CNS cryptococcosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
78
Q

Most common intracranial neoplasm in patients with AIDS

A

Primary CNS lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
79
Q

Region of the brain that is most severely involved in HIV encephalopathy

A

Centrum semiovale

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
80
Q

Region of the brain that is spared in HIV encephalopathy
“No sHIVs (weapon) allowed in the grey courtroom”

A

Cortical gray matter

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
81
Q

Region of the brain that is spared in herpes simplex encephalitis

A

Putamen

“Walang Herpes yung Puta”
“Yung Puta Walang Herpes”
Herpes simplex encephalitis spares Putamen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
82
Q

Most common manifestation of HIV infection of the brain on neuroimaging studies

A

Diffuse atrophy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
83
Q

This is the favored site of CNS toxoplasmosis

A

Basal ganglia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
84
Q

Difference between DEMYELINATION versus DYSMYELINATION

A

DEMYELINATION = Acquired, Adult, Affects normal myelin

DYSMYELINATION = Inherited, Pedia, Affects formation and maintenance of myelin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
85
Q

This refers to small infarcts (5-10mm) occurring within the basal ganglia typically over two-thirds of the putamina

A

Lacunae / Lacunar infarcts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
86
Q

Most common fatal encephalitis

A

Herpes encephalitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
87
Q

Most common neurodegenerative disease

A

Alzheimer disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
88
Q

Most common cause of dementia

A

Alzheimer disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
89
Q

Most common of the leukodystrophies

A

Metachromatic leukodystrophy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
90
Q

This is also called subacute necrotizing encephalomyelopathy. Involves a mitochondrial enzyme defect. In contrast to Wernicke encephalopathy, there is sparing of the mammillary bodies

A

Leigh disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
91
Q

This is also known as hepatolenticular degeneration. There is an inborn error of copper metabolism that is associated with hepatic cirrhosis and degenerative changes of the basal ganglia.

A

Wilson disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
92
Q

Intracorneal deposit of copper is virtually diagnostic of the Wilson disease when present

A

Kayser-Fleischer ring

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
93
Q

The most common basal ganglia disorder and one of the leading causes of neurologic disability in individuals older than age 60

A

Parkinson disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
94
Q

This neurotransmitter is deficient in parkinson’s disease due to dysfunction of the neuronal system specifically pars compacta of the substantia nigra

A

Dopamine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
95
Q

Postinfectious and postvaccinal encephalomyelitis. Typically occurs after a viral illness or vaccination.

A

Acute Disseminated Encephalomyelitis (ADEM)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
96
Q

Reactivated slowly progressive infection caused by the measles virus. Presents with patchy areas of periventricular demyelination as well as lesions of the basal ganglia.

A

Subacute Sclerosing Panencephalitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
97
Q

Represents a reactivation of a latent JC polyomavirus. Seen in immunocompromised individuals and typically involves the deep cerebral white matter with subcortical U-fiber involvement but spares cortex and deep gray matter.

A

Progressive Multifocal Leukoencephalopathy (PML)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
98
Q

Presents as subacute encephalitis in immunocompromised patients. Characterized clinically by a progressive dementia without focal neurologic signs. Causes focal or diffuse white matter hyperintensities on T2WI.

A

HIV encephalopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
99
Q

Most common electrolyte abnormality associated with central pontine myelinolysis

A

Hyponatremia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
100
Q

Most common cause of Wernicke encephalopathy and Korsakoff syndrome

A

Thiamine (B1) deficiency secondary to poor oral intake in SEVERE CHRONIC ALCOHOLISM

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
101
Q

Refers to a supraclinoid obliterative arteriopathy that occurs primarily in children and idiopathic in nature. Also known as “Puff of smoke”

A

Moyamoya disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
102
Q

Clinical triad of Wernicke encephalopathy

A
  1. Ocular movement abnormalities
  2. Ataxia
  3. Confusion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
103
Q

Persistent learning and memory deficits present in Wernicke encephalopathy

A

Wernicke-Korsakoff syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
104
Q

What is the dysmyelinating disease with the following description:
- autosomal recessive pattern
- arylsulfatase deficiency
- infantile type (MC)
- 2 y/o, gait disorder, mental deterioration
- progressive with sparing of subcortical U-fibers

A

Metachromatic Leukodystrophy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
105
Q

This type of hydrocephalus occurs when there is obstruction within the ventricular system and prevent CSF from exiting the ventricles

A

Non-communicating hydrocephalus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
106
Q

This type of hydrocephalus has an obstruction that is beyond the ventricular system it is located instead within the subarachnoid space

A

Communicating hydrocephalus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
107
Q

Most sensitive indicator for hydrocephalus

A

Enlargement of the temporal horns

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
108
Q

Most frequent causes of acute hydrocephalus

A

Subarachnoid hemorrhage and meningitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
109
Q

Colloid cyst typically block CSF flow in what level / portion

A

3rd ventricle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
110
Q

Pineal tumors and tectal gliomas typically obstruct CSF flow at what level / portion

A

Aqueduct

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
111
Q

Ependymoma and medulloblastomas typically interrupt CSF flow at the level of the

A

4th ventricle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
112
Q

Source of the majority of hemorrhages in premature infants

A

Germinal matrix

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
113
Q

Most common clinical finding of ischemic perinatal stroke

A

Focal neonatal seizures

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
114
Q

Most common cause for small amounts subarachnoid, subdural blood, or interventricular blood in the term newborn

A

Normal delivery / Traumatic normal delivery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
115
Q

Most severe form of holoprosencephaly

A

Alobar holoprosencephaly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
116
Q

Form of holoprosencephaly with an appearance of a horseshoe or cup-shaped interior rind of brain tissue, dominant single monoventricle that communicates with a posterior cyst. The corpus callosum interhemispheric fissure and falx cerebri or entirely absent.

A

Alobar holoprosencephaly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
117
Q

Most severe malformation resulting from an arrest of neuronal migration. Also known as “smooth brain”

A

Lissencephaly
“gLISSENingly smooth”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
118
Q

Most common chiari malformation

A

Chiari I (1)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
119
Q

Most rare chiari malformation

A

Chiari III (3)
“rar3st chiari malformation”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
120
Q

Most common of the phakomatoses

A

Neurofibromatosis Type 1 (Von Recklinghausen disease)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
121
Q

Chiari malformation associated with myelomeningocele/s

A

Chiari II (2)

“Dalawang Yelo”
Chiari II - myelomeningocele

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
122
Q

Chiari malformation associated with encephaloceles

A

Chiari III (3)
“3nc3phaloc3l3s”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
123
Q

Chiari malformation associated with cerebellar hypoplasia

A

Chiari IV (4)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
124
Q

Chiari malformation associated with cerebellar agenesis with occipital lobe herniation

A

Chiari V (5)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
125
Q

Chiari malformation associated with normal posterior fossa

A

Chiari IV (4)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
126
Q

Most common neurologic symptom of tuberous sclerosis

A

Epilepsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
127
Q

Most frequent brain lesions seen in tuberous sclerosis

A

Subependymal hamartomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
128
Q

Most common pathology involved in the paranasal sinuses and nasal cavity

A

Sinusitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
129
Q

Autosomal dominant disorder associated with retinal angiomas and cerebellar and spinal hemangioblastomas

A

Von Hippel-Lindau Syndrome (VHL)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
130
Q

A syndrome also known as Encephalotrigeminal angiomatosis, Associated with Port-wine nevus and Pial angiomatosis (gyral calcification, gyral atrophy and gliosis)

A

Sturge-Weber Syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
131
Q

Most common sinus involved with mucus retention cyst

A

Maxillary sinus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
132
Q

Most common sinus involved with Mucocele

A

Frontal sinus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
133
Q

Most common disease involving the temporal bone

A

Cholesteatoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
134
Q

Most common type of cholesteatoma, congenital or acquired?

A

Acquired (98%)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
135
Q

Most common site for formation of an acquired cholesteatoma

A

Superior portion of tympanic membrane (Pars flaccida = retracts easily)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
136
Q

Most common benign neoplasm arising of the minor salivary glands

A

Pleomorphic adenoma (Benign mixed-cell tumor)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
137
Q

Most common MINOR salivary gland malignancy

A

Adenoid cystic carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
138
Q

Most common malignancy of the aerodigestive tract

A

Squamous cell carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
139
Q

Most common variation in the vascular anatomy of the neck

A

Asymmetry of the internal jugular veins (RIGHT vein is LARGER)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
140
Q

Principal malignancy of the carotid space

A

Squamous cell nodal metastasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
141
Q

Most common tumor of the parotid gland

A

Pleomorphic adenoma (Benign mixed cell tumors)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
142
Q

A mass in the carotid space will displace the parapharyngeal space in what direction?

A

Anteriorly

Mnemonic for Normal:
“a Carrot Must Pair Superficially on my P.A.L.M”

Carrot = Carotid space ( P = Posterior to PPS)
Must = “Must”icator space ( A = Anterior to PPS)
Pair = “Pair”otid space ( L = Lateral to PPS)
Superficially = Superficial mucosal space ( M = Medial to PPS)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
143
Q

This neck space serves as a potential conduit for the spread of tumor or infection from the pharynx to the mediastinum. A.k.a “Danger space”

A

Retropharyngeal space

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
144
Q

These structures give rise to most pathologies in the prevertebral space

A

Cervical vertebral bodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
145
Q

Most common tumor of the optic nerve and typically occurs during the first decade of life

A

Optic nerve glioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
146
Q

This tumor arises from hemangioendothelial cells of the arachnoid layer of the optic nerve sheath. It assumes a circular configuration and grows into a linear fashion along the optic nerve. It demonstrates a tram track pattern of linear contrast enhancement. It may be extensively calcified.

A

Optic sheath meningioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
147
Q

Most common cause of intraorbital mass lesion in the adult

A

Idiopathic inflammatory pseudotumor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
148
Q

The most frequent cause of unilateral or bilateral proptosis in adults

A

Thyroid ophthalmopathy (Graves disease)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
149
Q

Muscles involved in decreasing order of frequency in graves’ disease
“IM SLow”

A

“I’M SLow”
Inferior rectus (most involved)
Medial rectus
Superior rectus
Lateral rectus (least involved)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
150
Q

Most common primary ocular malignancy in the pediatric age group and presents characteristically with leukocoria and a calcified ocular mass

A

Retinoblastoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
151
Q

Most common neck malignancy in the pediatric age group

A

Lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
152
Q

Most common congenital neck lesion in children

A

Thyroglossal duct cyst

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
153
Q

Most common midline neck mass

A

Thyroglossal duct cyst

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
154
Q

Most branchial cleft cysts arise from which branchial cleft

A

Second branchial cleft (95%)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
155
Q

Classic symptoms of Myelopathy
“kapag Myelopathy, B.A.W.a.S”

A

“kapag Myelopathy, B.A.W.a.S”
- Bladder & Bowel Incontinence
- Ataxia
- Weakness
and
- Spasticity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
156
Q

Most common spinal causes of pain and neurologic deficit are

A
  • Disc herniations
  • Uncovertebral joint spurring
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
157
Q

Most common spinal cord “inflammatory” disorder

A

Multiple sclerosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
158
Q

Most common cause of intramedullary lesions

A

Multiple sclerosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
159
Q

Currently the most common cause of arachnoiditis

A

Iatrogenic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
160
Q

Most common site of hematogenous infectious seeding in the spine

A

Vertebral body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
161
Q

Most common cause of spine infection in adults

A

Staphylococcus aureus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
162
Q

This is also known as tuberculosis of the spine. Associated with slow collapse of one or more vertebral bodies resulting in acute kyphosis or “gibbus” deformity. Cord compression may occur as a result of this gibbus deformity

A

Pott disease / Pott’s disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
163
Q

The term “cold abscess” describes large spinal abscesses without severe pain or frank pus is associated with what disease?

A

Pott disease / Pott’s disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
164
Q

Most common spinal cord tumor in adults

A

Ependymomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
165
Q

Most common spinal cord tumor in children

A

Astrocytoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
166
Q

Most common intradural tumor in the thoracic region and represents roughly 25% of all adult intraspinal tumors

A

Meningioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
167
Q

Most common intraspinal mass. It is also the most common nerve sheath tumor

A

Schwannoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
168
Q

Classic cause of spinal intradural extramedullary metastases

A

Subarachnoid seeding of primary CNS neoplasm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
169
Q

Spinal cord split into two hemicords by a sagittal bony or cartilaginous spur. Most occur in the lower thoracic region and are accompanied by vertebral segmentation abnormalities

A

Diastematomyelia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
170
Q

Most common site in the spine for root avulsion

A

Cervical spine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
171
Q

Most common cause of neuroforaminal stenosis

A

Degenerative disease of the facets with bony hypertrophy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
172
Q

Most common cause of central canal stenosis and lateral recess stenosis

A

Degenerative disease of the facets with bony hypertrophy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
173
Q

Most common modic type endplate changes

A

Modic type 2
- replacement of red marrow with fatty yellow marrow
- T1 High, T2 High

Other Modic Types:
Modic type 1
- marrow edema and inflammation
- response to degenerative disc disease
- can also be a sign of infection
- T1 Low, T1 High

Modic type 3
- Bony sclerosis
- T1 Low, T2 Low

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
174
Q

Most common form of atelectasis

A

Obstructive or resorptive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
175
Q

Most common causes of endobronchial obstruction and secondary resorptive atelectasis

A
  • bronchogenic carcinoma
  • foreign bodies
  • mucus plugs
  • malpositioned endotracheal tube
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
176
Q

Type of atelectasis associated with chronic tuberculosis

A

Cicatricial atelectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
177
Q

Type of atelectasis associated with surfactant deficiency

A

Adhesive atelectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
178
Q

The only DIRECT radiographic finding of lobar atelectasis

A

Displacement of an interlobar fissure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
179
Q

Type of atelectasis that is usually found along the inferior and posterior costal pleural surfaces adjacent to an area of pleural fibrosis or plaque formation. Identified also by a curvilinear bronchovascular tube or “comet tail” entering the anterior inferior margin of the mass

A

Round atelectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
180
Q

Atelectasis of this lobe produces the S sign of golden

A

Right upper lobe atelectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
181
Q

What sign will be produced when there is collapse of the right upper lobe superiorly and medially, superomedial displacement of the minor fissure and anteromedial displacement of the major fissure

A

S sign of Golden

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
182
Q

What lobes are atelectatic when there is obstruction of the bronchus intermedius by a mucus plug or tumor

A

Combined right middle and right lower lobe atelectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
183
Q

Which lung lobe is commonly collapsed in patients with large hearts and in postoperative patients, particularly, who have had coronary bypass surgery

A

Left lower lobe atelectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
184
Q

Pulmonary edema and interstitial pneumonitis will present with this type of reticular pattern of opacities

A

Fine reticular “Ground glass pattern”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
185
Q

Pulmonary fibrosis will most commonly present with this type of reticular pattern of opacities

A

Medium reticular “Honeycombing”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
186
Q

Nodular opacities <2 mm

A

Miliary opacities

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
187
Q

Nodular opacities 2-7mm

A

Micronodules

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
188
Q

Nodular opacities 7-30mm

A

Nodules

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
189
Q

Nodular opacities >30mm

A

Masses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
190
Q

Diseases that give rise to TRUE RETICULONODULAR opacities

A
  • Silicosis
  • Sarcoidosis
  • Lymphangitic carcinomatosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
191
Q

What type of kerley lines are obliquely oriented, course toward the hila, measure 2-6 cm long and with <1 mm thickness.

A

Kerley A lines

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
192
Q

What type of Kerley lines are peripherally located, coarse, perpendicular to and contact the pleural surface, and measure about 1-2 cm.

A

Kerley B lines

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
193
Q

Kerly lines that represent thickened peripheral subplural interlobular septa

A

Kerley B lines

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
194
Q

Kerly lines that correspond to thickening of connective tissues sheets within the lung which contain lymphatic communications between the perivenous and bronchoarterial lymphatics

A

Kerley A lines

Ker-lymph-A-tics = kerly A lines

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
195
Q

Most common cavitary pulmonary lesions

A

Lung abscess and necrotic neoplasm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
196
Q

A collection of gas <1 cm in size within the layers of the visceral pleura. It is usually found in the apical portion of the lung. Its rupture can lead to spontaneous pneumothorax

A

Blebs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
197
Q

Gas collection within the pulmonary parenchyma >1 cm in diameter and a thin wall of <1 mm thick. It represents a focal area of parenchymal destruction like emphysema and may contain fibrous strands, residual blood vessels, or alveolar septa.

A

Bullae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
198
Q

Thin-walled gas containing structures that represent distended airspaces distal to a check valve obstruction of a bronchus or bronchiole. It is most commonly secondary to staphylococcal pneumonia

A

Pneumatoceles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
199
Q

Any well-circumscribed intrapulmonary gas collection with a smooth thin wall >1 mm thick

A

Air cyst (Brant 5th ed)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
200
Q

This syndrome involves congenital absence of the pectoralis muscle which produce a unilateral pulmonary hyperlucency

A

Poland syndrome

P-oland syndrome
P-ectoralis muscle absence
P-ulmonary lucency (unilateral)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
201
Q

This syndrome is a condition that follows adenoviral infection during infancy. It is also known as unilateral hyperlucent lung. This will produce a TRUE unilateral hyperlucent lung.

A

Swyer-James syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
202
Q

Diseases that may manifest as bilateral hyperlucent lungs

A
  • Emphysema
  • Asthma
  • PS associated with TOF
  • Obstruction of pulmo circulation (PAH, Chronic thromboembolic disease)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
203
Q

Most common finding of pneumomediastinum

A

Air outlining the left heart border

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
204
Q

Air dissects between the pericardium above the central diaphragm below to allow visualization of central portion of the diaphragm

A

Continuous diaphragm sign

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
205
Q

This sign indicates that a mass is superimposed on the hilum and normal hilar vessels can be seen through the density

A

Hilum overlay sign

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
206
Q

This sign indicates enlargement of the intrahilar vascular structures. Vascular structures converge only as far as the lateral margin the increased higher density

A

Hilum/Hilar convergence sign

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
207
Q

To differentiate pleural effusion from ascites on Axial CT

A

Pleural Effusion displaces Crus LATERALLY “PE.C.LAT”

Ascites displaces CRUS MEDIALLY (Opposite of Pleural effusion)
“A.C.MED)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
208
Q

Most common thoracic inlet mass seen in older patients

A

Tortuous arterial structures / Tortuous aorta

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
209
Q

Enlargement of a thymus that is normal on gross and histologic examination. This occurs primarily in children as a rebound effect.

A

Thymic hyperplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
210
Q

This is a neuroendocrine tumor of the thymus. It is a rare malignant neoplasm believed to arise from the thymic cells of neural crest origin (APUD or Kulchitsky cells). Carcinoid tumor is the most common histologic type.

A

Thymic carcinoid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
211
Q

In lymphoma, this is the most frequent site of a localized nodal mass in which portion of the mediastinum particularly those of nodular sclerosing type

A

Anterior mediastinum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
212
Q

Most common subtypes of non-hodgkin’s lymphoma

A

Lymphoblastic lymphoma and diffuse large b-cell lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
213
Q

This type of lymphoma most commonly involves the middle mediastinal and hilar lymph nodes

A

Non-hodgkin lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
214
Q

This type of lymphoma most commonly involves the anterior mediastinal and hilar nodal groups

A

Hodgkin lymphoma

H-odgkin = H-arap (Anterior and Hilar nodal groups)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
215
Q

This is the most common primary mediastinal neoplasm in adults

A

Lymphoma, either Hodgkin or Non-Hodgkin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
216
Q

Treatment for localized intrathoracic hodgkin disease

A

Radiation / Radiotherapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
217
Q

Treatment for non-hodgkin’s lymphoma and widespread hodgkin disease

A

Chemotherapy (Better response rates for Hodgkin than NHL)

“Radio Hud” Radiotherapy for Hodgkins
“Kimochi, Non-hentai!” Chemotherapy for Non-Hodgkins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
218
Q

Most common benign mediastinal germ cell neoplasm

A

Teratoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
219
Q

Most common type of teratoma seen in the mediastinum

A

Cystic or mature teratoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
220
Q

This neoplasm contains only elements derived from the ectodermal germinal cyst

A

Dermoid cyst

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
221
Q

This type of teratoma commonly contains tissues of epidermal, dermal, and endodermal origins

A

Mature or Cystic teratoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
222
Q

Most common malignant germ cell neoplasm

A

Seminoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
223
Q

Most common source of metastases to the middle mediastinal nodes

A

Bronchogenic carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
224
Q

Bronchogenic carcinoma will metastasize specifically to which middle mediastinal nodes?

A

Paratracheal and aorticopulmonary nodes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
225
Q

Pericardial cysts most commonly arise from

A

Anterior cardiophrenic angle (right sided lesions twice as common as left cardiophrenic angle)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
226
Q

Neurogenic tumors arising from intercostal nerves

A

Neurofibroma, Schwannoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
227
Q

Neurogenic tumors arising from the sympathetic ganglia

A

Ganglioneuroma, Ganglioneuroblastoma, Neuroblastoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
228
Q

Neurogenic tumors arising from paraganglionic cells

A

Pheochromocytoma, Chemodectoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
229
Q

Non-functioning paraganglioma

A

Chemodectomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
230
Q

Functioning paraganglioma

A

Pheochromocytoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
231
Q

Most common structure in a hiatal hernia sac

A

Stomach

Cardia in SLIDING HERNIA “Sliding Car”
Fundus in PARAESOPHAGEAL HERNIA “PARA is FUN to use (Counterstrike)”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
232
Q

Paraspinal masses produced by expansion of the vertebral body or posterior elements

A

Multiple myeloma, Aneurysmal bone cyst

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
233
Q

Most common primary malignancies that metastasize to the thoracic spine

A

Bronchogenic, breast, or renal cell carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
234
Q

Most common posterior mediastinal mass in patients with neurofibromatosis

A

Meningocele

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
235
Q

Most common cause of chronic sclerosing fibrosing mediastinitis

A

Granulomatous infection secondary to histoplasma capsulatum

Other less common causes include:
Tuberculous, Radiotherapy, Drugs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
236
Q

Most commonly affected structure in chronic sclerosing fibrosing mediastinitis

A

Superior vena cava (75% of symptomatic patients)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
237
Q

SVC syndrome manifests with…

A

Jugular venous distention, Cyanosis, Edema, Headache, Epistaxis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
238
Q

Most serious and potentially fatal manifestation of chronic sclerosing fibrosing mediastinitis

A

Obstruction of central pulmonary veins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
239
Q

Most common cause of mediastinal hemorrhage

A

Trauma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
240
Q

Most common source of pneumomediastinum

A

Air from the lungs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
241
Q

Pneumomediastinum - Extra-alveolar air collects within bronchovascular interstitium which dissects centrally to the hilum and mediastinum

A

Macklin effect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
242
Q

Substernal chest pain caused by intramediastinal extension of infections

A

Ludwig angina

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
243
Q

Extrathoracic neoplasm with the highest incidence of intrathoracic nodal metastases

A

Malignant melanoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
244
Q

Most common thoracic radiographic manifestation of lymphoma

A

Hilar and mediastinal lymph node enlargement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
245
Q

Most common form of pulmonary edema

A

Hydrostatic pulmonary edema (Normal capillary permeability)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
246
Q

PCWP range with findings of constriction of lower vessels and enlargement of upper lobe vessels

A

PCWP 12-18 mmHg (Mild elevation)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
247
Q

PCWP range with findings of interstitial edema, loss of vascular definition, peribronchial cuffing, and Kerley lines

A

PCWP 19-25 mmHg (Progressive elevation)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
248
Q

PCWP range with findings of alveolar filling with radiographic findings of bilateral airspace opacities in the perihilar and lower lung zones

A

PCWP above 25 mmHg

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
249
Q

PCWP normal range

A

PCWP 8-12 mmHg

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
250
Q

Most common finding in pulmonary embolism without infarction

A

Peripheral airspace opacities and linear atelectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
251
Q

Sign of pulmonary embolism - Regional oligemia (decreased pulmo blood flow) and has the highest positive predictive value / highest sensitivity

A

Westermark sign

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
252
Q

Pulmonary embolism - peripheral wedge of airspace opacity and implies lung infarction

A

Hampton hump

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
253
Q

Pulmonary embolism - sign of enlarged Pulmonary Artery

A

Fleischner sign

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
254
Q

Hallmark of pulmonary embolism

A

Ventilation/perfusion mismatch (V/Q mismatch)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
255
Q

Traditionally considered to be the gold standard in the diagnosis of pulmonary embolism

A

Pulmonary angiography

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
256
Q

Widely considered the first-line diagnostic modality for the evaluation of suspected pulmonary embolism

A

MDCT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
257
Q

Most common cause of pulmonary arterial hypertension

A

Increase in resistance to pulmonary blood flow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
258
Q

Identification of feeding and draining vessels emanating from the hilar aspect of a solitary pulmonary nodule is pathognomonic of this

A

Pulmonary Arteriovenous malformation (AVM)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
259
Q

Presence of halo of ground glass opacity encircling a solitary pulmonary nodule in an immunocompromised or neutropenic patient

A

Invasive pulmonary aspergillosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
260
Q

A nodule or mass adjacent to an area of pleural thickening with a “comet tail” of bronchi and vessels entering the higher aspect of the mass and associated with lobar volume loss

A

Round atelectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
261
Q

The single most important factor in characterizing the lesion as benign or indeterminate

A

Internal density of a mass/nodule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
262
Q

Most common type of lung cancer, accounting for 1/3 of all bronchogenic carcinoma

A

Adenocarcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
263
Q

Most common subtype of lung cancer in non-smokers

A

Adenocarcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
264
Q

Most malignant neoplasms arising from bronchial neuroendocrine (Kulchitzky) cells and are alternatively referred to as Kulchitzky cell cancers or KCC-3

A

Small cell carcinoma

“Kulit-zky ng mga Maliit na bata” (Kulchitzky cells, Small Cell Carcinoma)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
265
Q

Bronchogenic carcinoma associated with cavitation of solitary malignant nodules

A

Squamous cell carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
266
Q

Bronchogenic carcinoma associated with air bronchograms or bubbly lucency within a nodular mass

A

Adenocarcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
267
Q

Most common cause of SVC syndrome

A

Lung cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
268
Q

Most common primary tracheal malignancy

A

Squamous cell carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
269
Q

Majority of tracheal neoplasms arise from which portion of the trachea

A

Distal trachea, within 3 to 4 cm of the tracheal carina

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
270
Q

Most common types of thyroid malignancy to invade the trachea

A

Papillary and follicular carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
271
Q

Most common pattern of pulmonary infection

A

Lobular or bronchopneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
272
Q

Most common cause of multifocal patchy airspace opacities

A

Bronchopneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
273
Q

Pulmonary infection represents radiographically as multifocal opacities that are roughly lobular in configuration which produce a “patchwork quilt” appearance because of the interspersion of normal and diseased lobules

A

Lobular or bronchopneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
274
Q

Typical radiographic appearance for acute pneumococcal pneumonia

A

Lobar consolidation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
275
Q

In children, pneumococcal pneumonia present as a spherical opacity simulating a parenchymal mass

A

Round pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
276
Q

Most common type of pneumonia in hospitalized and debilitated patients

A

Staphylococcus aureus pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
277
Q

This type of pneumonia may develop following hematogenous spread to the lung in patients with endocarditis or indwelling catheters and in intravenous drug users

A

Staphylococcus aureus pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
278
Q

In this type of pneumonia, children may develop pneumatocele information

A

Staphylococcus aureus pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
279
Q

Used as an agent of bioterrorism in the united states. CT scan will show high attenuation lymphadenopathy and pleural effusion secondary to hemorrhage. Radiographic manifestations include:
- hemorrhagic lymphadenitis and mediastinitis
- hemorrhagic pleural effusions

A

Bacillus anthracis (Anthrax)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
280
Q

Pneumonia with bulging interlobular fissure. “Bulging fissure” sign. Incidence of effusion and empyema is higher

A

Klebsiella pneumoniae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
281
Q

Pneumonia with etiologic agent commonly found in air conditioning and humidifier systems. Produces airspace opacification that is initially peripherally located and sublobar

A

Legionnaires disease, L. Pneumophilia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
282
Q

Anaerobic gram positive filamentous bacterium. Part of normal flora of human oropharynx. Most commonly follows dental extractions manifesting as mandibular osteomyelitis or a soft tissue abscess.

A

Actinomyces israelii

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
283
Q

Most common atypical pneumonia

A

Mycoplasma pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
284
Q

An important radiographic feature and indicates active and transmissible disease in tuberculosis

A

Cavitation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
285
Q

Tuberculous infiltrates can erode into a branch of pulmonary artery can produce aneurysm and cause hemoptysis

A

Rasmussen aneurysm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
286
Q

Consists of a calcified parenchymal nodule (Ghon complex) and nodal calcification

A

Ranke complex in Primary TB

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
287
Q

Most common organism responsible for atypical mycobacterial infection

A

Mycobacterium avium-intracellulare (MAI) or M.kansasii

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
288
Q

Most common cause of viral pneumonia in adults

A

Influenza

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
289
Q

Most common method of pleuropulmonary involvement by amoebiasis

A

Direct intrathoracic extension from a hepatic abscess

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
290
Q

Etiologic agent involved in most cases of human hydatid disease

A

Echinococcus granulosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
291
Q

Definitive hosts for Echinococcosis / Hydatid cyst

A

Dogs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
292
Q

Intermediate hosts for Echinococcosis / Hydatid cyst

A

Sheep

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
293
Q

Accidental hosts for Echinococcosis / Hydatid cyst

A

Humans

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
294
Q

Most important parasitic infections of humans worldwide

A

Schistosomiasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
295
Q

Most common complication of pneumonia and it is seen in 50% of patients

A

Parapneumonic effusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
296
Q

Most common cause of pneumonia in immunocompromised hosts

A

Bacterial pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
297
Q

The most common non-tuberculous mycobacterial infection in patients with AIDS

A

Mycobacterium avium intracellulare (MAI)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
298
Q

Most common cause of fungal infection in the AIDS population

A

Cryptococcosis, C.neoformans

  • a budding yeast commonly found in soil and bird droppings
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
299
Q

Most serious consequence of cryptococcosis

A

Meningitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
300
Q

The most common AIDS defining opportunistic infection. Most common in patient with AIDS usually those in the late stages of HIV infection with CD4 counts of < 200 cells/mm3

A

Pneumocystis jiroveci pneumonia (formerly Pneumocystis carinii pneumonia, PCP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
301
Q

This obligate intracellular protozoan has cats as definitive hosts and spreads via ingestion of material contaminated by oocyst containing stool

A

Toxoplasma gondii, Toxoplasmosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
302
Q

Most common pleural manifestation of rheumatoid disease and is found in 20% of patients

A

Pleuritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
303
Q

Syndrome wherein nodules develop in the lungs of coal miners and silica or asbestos workers with rheumatoid arthritis as a hypersensitivity response to inhaled dust particles

A

Caplan syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
304
Q

Sicca syndrome

A

Dry eyes (Xerophthalmia/Keratoconjunctivitis sicca)
Dry nose (Xerorhinia)
Dry mouth (Xerostomia)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
305
Q

Autoimmune disorder of middle-aged women and characterized by the Sicca syndrome

A

Sjogren syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
306
Q

Most common pulmonary manifestation of Sjogren syndrome

A

Interstitial fibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
307
Q

Most common of the idiopathic interstitial pneumonia

A

Usual interstitial pneumonia (UIP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
308
Q

Type of interstitial pneumonia with a histologic feature of temporal heterogeneity, wherein different stages of the disease are seen simultaneously within the different portions of the lung.

A

Usual interstitial pneumonia (UIP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
309
Q

Type of interstitial pneumonia also known as Hamman-Rich syndrome. It is an acute aggressive form of idiopathic interstitial pneumonitis and fibrosis. Histologic findings of diffuse alveolar damage with minimal mature collagen deposition which are diffuse and temporarily homogeneous. Manifests as ARDS with diffuse GGO and consolidation with air bronchograms.

A

Acute interstitial pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
310
Q

Chronic interstitial lung disease with pathology of smooth muscle proliferation in peribronchovascular and parenchymal interstitium.

A

Tuberous sclerosis (TS)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
311
Q

Classic triad of tuberous sclerosis (in Chronic interstitial lung disease)
“MR S.Ad Tubero”

A
  1. Mental retardation
  2. Seizures
  3. Adenoma sebaceum
    ”MR S.Ad Tubero”
    Mental Retardation, Seizures, ADenoma sebaceum, TUBEROus sclerosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
312
Q

Chronic interstitial lung disease with pathology of smooth muscle proliferation within lymphatic channels

A

Lymphangioleiomyomatosis (LAM)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
313
Q

Chronic interstitial lung disease with development of chylothorax, chyloperitoneum or chylopericardium. May also produce chylous pleural effusions that are large and recurrent

A

Lymphangioleiomyomatosis (LAM)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
314
Q

Chronic interstitial lung disease that has a characteristic apple green color when stained with congo red under polarized light

A

Alveolar septal amyloidosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
315
Q

Chronic interstitial lung disease with manifestations of cutaneous cafe au lait spots, cutaneous and subcutaneous neurofibromas, scalloping of the posterior aspect of vertebral bodies with kyphoscioliosis. “Ribbon rib” and rib notching may be seen as well.

A

Neurofibromatosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
316
Q

Most common pleural manifestation of Asbestos inhalation

A

Parietal pleural plaques

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
317
Q

Type of idiopathic eosinophilic lung disease disease also known as loffler syndrome. This is a transient pulmonary process characterized by pulmonary infiltration with eosinophilic exudates. Opacities have been described as “fleeting” because there is a tendency for rapid clearing and one area with new involvement in other areas.

A

Simple pulmonary eosinophilia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
318
Q

Drugs associated with pulmonary eosinophilia
“Nitro Pencil”

A

Nitrofurantoin and penicillin
Nitro-furantoin, Pencil-lin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
319
Q

Parasitic infections associated with pulmonary eosinophilia
“A Scar is Strong”

A

Ascaris lumbricoides, Strongyloides stercoralis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
320
Q

This type of idiopathic eosinophilic disease is a systemic disorder with a male predominance. Characterized by multiple organ damage from eosinophilic infiltration.
There is marked and prolonged blood eosinophilia. Associated with cardiac involvement causing CHF, Cardiomegaly, Pulmonary edema and Pleural effusions

A

Hypereosinophilic syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
321
Q

Drug that cause diffuse alveolar damage
“Sabi ni mommy, nasa B.G.C. DAD MO”

A

B-leomycin
G-old
C-yclophosphamide
Diffuse Alveolar Damage
M-itomycin
O-piates

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
322
Q

Drugs causing Usual Interstitial Pneumonia
“B.A.N.Me” (Banh mi)

A

B-leomycin
A-miodarone (If with pulmonary edema, this drug is likely the culprit)
N-itrofurantoin
Me-thotrexate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
323
Q

Lipoproteinaceous material surfactant deposits in abnormal amounts within air space of the lungs. Associated with acquired defect of alveolar macrophages that fail to phagocytose surfactant resulting in accumulation of surfactant within alveolar spaces. Alveoli filled with lipoproteinaceous material that stains deep pink with periodic acid-Schiff.

A

Pulmonary alveolar proteinosis (PAP)

PAP
P-hagocytose failure
P-rogressive dyspnea
P-ink (Deep) on P-eriodic acid-Schiff
P-eripheral nodules
P-eripheral airspace opacification that is bilateral and symmetric

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
324
Q

Disorder characterized by deposition of minute calculi within the alveolar spaces. Produces a radiographic finding of confluent bilateral dense micronodular opacities (because of high interest of density) or “Black pleura sign”

A

Alveolar microlithiasis

Black pleura sign
= represent subpleural sparing of pulmonary calcification that occurs in the alveoli centrally. Seen as a strip of tangential peripheral lucency underlying the ribs as compared with adjacent diffusely dense calcified lung.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
325
Q

A congenital tracheal anomaly that is a true diverticula that represents herniation at the tracheal air column through a weakened posterior tracheal membrane

A

Tracheoceles / Paratracheal air cysts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
326
Q

Fixed deformity of the intrathoracic trachea in which the coronal diameter is diminished to less than two-thirds of the sagittal diameter. The tracheal wall is uniformly thickened and there is calcification of the cartilaginous rings. Present in older men with COPD.

A

Saber-sheath trachea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
327
Q

Characterized by presence of multiple submucosal osseous and cartilaginous deposits within the trachea and central bronchi of elderly men. The calcified plaques usually involve the anterior and lateral walls of the trachea with SPARING of the membranous POSTERIOR WALL of the trachea which lacks cartilage.

A

Tracheobronchopathia Osteochrondroplastica

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
328
Q

A systemic autoimmune disorder that commonly affects the cartilages in tracheobronchial tree, larynx, ear, nose, joints and large elastic arteries. Diagnosis made by noting RECURRENT inflammation at TWO OR MORE cartilaginous sites, most commonly the pinna of the ear (producing cauliflower ears) and the bridge of the nose (producing a saddle nose deformity)

A

Relapsing polychondritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
329
Q

A congenital disorder of the elastic and smooth muscle components of the tracheal wall. Abnormal compliance of the trachea and central bronchial collapse during coughing predisposing to recurrent pneumonia and bronchiectasis. On frontal radiographs, trachea and central bronchi measure greater than 3.0 and 2.0 cm respectively and coronal diameter.

A

Tracheobronchomegaly (Mounier-Kuhn syndrome)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
330
Q

Most common type of emphysema

A

Centrilobular emphysema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
331
Q

Most common etiologic factor associated with emphysema

A

Cigarette smoking

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
332
Q

Type of emphysema that is associated with deficiency of the serum protein alpha 1 antitrypsin (alpha 1 protease inhibitor)

A

Panlobular emphysema
“pANTItrypsin deficiency”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
333
Q

Most important plain radiographic finding in emphysema and reflects the loss of lung elastic recoil

A

Hyperinflation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
334
Q

Refers to an inflammation of the small non-cartilaginous airways

A

Bronchiolitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
335
Q

Most common condition to produce a transudative pleural effusion

A

Congestive heart failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
336
Q

Most common cause of parapneumonic effusion and empyema

A

Staphylococcus aureus and gram-negative pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
337
Q

Most common intrathoracic manifestation of rheumatoid arthritis

A

Pleural effusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
338
Q

Most common cause of pneumothorax

A

Trauma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
339
Q

Most common predisposing condition of secondary spontaneous pneumothorax

A

COPD

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
340
Q

Most common connective tissue disease producing pneumothorax; usually from rupture of an apical bullae

A

Marfan syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
341
Q

Most common inflammatory disease causing localized pleural thickening

A

Pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
342
Q

Defined as pleural thickening extending over more than 1/4 of the costal pleural surface. Most commonly results from resolution of an exudative pleural effusion, empyema, or hemithorax. May be seen as subpleural extension of diffuse interstitial fibrosis or encompass the entire lung producing entrapment.

A

Fibrothorax

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
343
Q

Most common benign manifestation of asbestos inhalation

A

Pleural plaques

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
344
Q

Earliest manifestation of asbestos-related pleural disease

A

Pleural effusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
345
Q

Type of fiber most often implicated in malignant mesothelioma and is most commonly encountered since it is most used in the industry

A

Crocidolite

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
346
Q

Most common histologic type of malignant mesothelioma and has the best prognosis among the different types

A

Epithelial

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
347
Q

Most common organisms responsible for chest wall abscesses

A

Staphylococcus and Mycobacterium tuberculosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
348
Q

Most common benign neoplasm of the chest wall

A

Lipoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
349
Q

Most common malignant soft tissue neoplasms of the chest wall in adults

A

Fibrosarcomas and Liposarcomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
350
Q

Most common congenital anomalies of the ribs

A

Bifid ribs and bony fusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
351
Q

Most common cause of bilateral inferior rib notching

A

Coarctation of the aorta

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
352
Q

Which ribs are UNINVOLVED in rib notching?

A

First two ribs

First and second intercostal arteries arise from the superior intercostal branch of the costocervical trunk of the subclavian artery, therefore do not communicate with the descending thoracic aorta.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
353
Q

Most common non-vascular cause of inferior rib notching

A

Multiple intercostal neurofibromas in Neurofibromatosis type 1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
354
Q

Most common site in the bony thorax involved by monostatic fibrous dysplasia

A

Ribs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
355
Q

Most common benign neoplasm of the ribs in adults

A

Osteochondroma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
356
Q

Most common primary rib malignancy

A

Chondrosarcoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
357
Q

Most common metastatic lesions to ribs

A

Bronchogenic and breast carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
358
Q

Most commonly produce sclerotic rib metastases

A

Breast and prostate carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
359
Q

This congenital deformity involves a hypoplastic scapula and is elevated

A

Sprengel deformity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
360
Q

The scapula is superiorly displaced and its inferior portion is posteriorly displaced. It results from disruption in the innervation of the serratus anterior muscle (long thoracic nerve) that maintains the scapula against the chest wall

A

Winged scapula, Winging of the scapula

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
361
Q

Most commonly fractured portion of the clavicle in blunt trauma

A

Distal third

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
362
Q

Primary malignant neoplasms of the clavicle

A

Ewing or Osteogenic sarcoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
363
Q

H-shaped or “Lincoln log” vertebrae on lateral chest and is pathognomonic of this disease

A

Sickle cell anemia

“Lincoln’s Sickle cut H-shaped Log”
Lincoln Log vertebrae, Sickle cell anemia, H-shaped vertebrae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
364
Q

“Rugger jersey” appearance of the thoracic spine on lateral chest films

A

Hyperparathyroidism, Renal osteodystrophy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
365
Q

“Sandwich vertebral body” or “Sandwich vertebrae” represents densely sclerotic endplates of vertebral bodies distinctive for which disease

A

Osteopetrosis, a benign autosomal dominant disorder

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
366
Q

Paradoxical superior movement of the diaphragm with sniffing. A result of the effects of negative intrathoracic pressure on a flaccid diaphragm during inspiration is diagnostic

A

Positive sniff test

Usually done for Diaphragmatic paralysis (Unilateral or Bilateral)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
367
Q

Most common type of diaphragmatic hernia

A

Hiatal hernia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
368
Q

Most common structure to herniate in a hiatal hernia

A

Stomach

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
369
Q

Least common type of diagphragmatic hernia

A

Morgagni hernia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
370
Q

Most common primary malignant diaphragmatic lesion

A

Fibrosarcoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
371
Q

Most commonly involved segment of lung in bronchial atresia

A

Apicoposterior segment of the left upper lobe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
372
Q

Most commonly involved segment of the lung in neonatal lobar hyperinflation (congenital lobar emphysema)

A

Left upper lobe (most common)

Right middle lobe (2nd most common)
Right upper lobe (3rd)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
373
Q

Congenital abnormality resulting from the INDEPENDENT development of a portion of the tracheobronchial tree that is ISOLATED from the normal lung and maintains its fetal systemic arterial supply. The isolated lung is cystic and bronchiectatic. Patients will present with recurrent pneumonia.

A

Bronchopulmonary sequestration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
374
Q

Type of bronchopulmonary sequestration:
- Contained within visceral pleura of normal lung
- Present with pneumonia (most)
- Found in lower lobes
- Supplied by a single large artery

A

Intralobar sequestration

More common than extralobar (3:1)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
375
Q

Most common pulmonary symptoms of arteriovenous malformations

A

Hemoptysis and dyspnea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
376
Q

This syndrome describes massive aspiration of gastric contents

A

Mendelson syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
377
Q

Used to monitor response to chemotherapy of lymphoma

A

CT and Fluorodeoxyglucose (FDG) PET

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
378
Q

Replaced by FDG PET in the initial diagnosis and staging of thoracic lymphoma

A

SPECT - Radionuclide scintigraphy with gallium-67

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
379
Q

Superior to CT or MRI in distinguishing recurrent tumor from fibrosis in both hodgkins and non-hodgkins lymphoma

A

PET

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
380
Q

Diagnostic for functioning neoplasms such as pheochromocytoma

A

PET radionuclide iodine-131

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
381
Q

Diagnostic for pulsion diverticula

A

Barium swallow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
382
Q

Used for staging of esophageal carcinoma

A

CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
383
Q

Provides a definitive diagnosis of mediastinal lipomatosis

A

CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
384
Q

Provides superior accuracy in the nodal staging of lung CA

A

PET

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
385
Q

Useful in characterizing pleural effusions in patients with lung cancer as malignant

A

PET

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
386
Q

Used to detect metastases of bronchogenic carcinoma

A

Technetium 99, radionuclide bone scanning or whole-body FDG-PET

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
387
Q

Methods used to distinguish adenomas from malignant (primary metastatic) adrenal lesions

A

CT scan, Chemical shift MRI, FDG-PET, FNAB

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
388
Q

Best imaging modality to follow response of metastases to chemotherapy

A

CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
389
Q

Modality used to distinguish Kaposi sarcoma from pneumonia and non-hodgkin’s lymphoma

A

Combined thallium and gallium lung scanning

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
390
Q

Diagnosis of PCP in AIDS

A

Sputum samples or bronchoalveolar lavage fluid specimens with methanamine silver staining

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
391
Q

Method of choice for the diagnosis of a mediastinal cyst

A

CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
392
Q

Modality of choice for imaging a suspected neurofibroma

A

MRI

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
393
Q

Diagnostic technique of choice for lateral thoracic meningoceles

A

MRI

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
394
Q

Radiologic study of choice for the diagnosis of acute mediastinitis

A

MDCT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
395
Q

Modality of choice for the diagnosis of chronic sclerosing mediastinitis

A

CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
396
Q

First-line diagnostic modality for the evaluation of suspected pulmonary embolism

A

MDCT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
397
Q

Traditional considered to be the gold standard in the diagnosis of pulmonary embolism

A

Pulmonary angiography

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
398
Q

Procedure of choice for tissue sampling of a solitary pulmonary nodule

A

Transthoracic needle biopsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
399
Q

Modality of choice for imaging tracheal neoplasms

A

CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
400
Q

Modality of choice for evaluation of pulmonary metastases

A

Helical CT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
401
Q

Definitive diagnostic procedure as it demonstrates relationship of mass with pulmonary arterial vasculature

A

Contrast enhanced CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
402
Q

Diagnostic imaging modality of choice for broncholithiasis

A

Thin section CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
403
Q

Modality of choice in the evaluation of malignant mesothelioma and depicts the extent of pleural involvement and invasion of the chest wall and mediastinum

A

CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
404
Q

Modality of choice in the evaluation of sternal wound infection

A

CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
405
Q

Most common histologic type of thymic carcinoid

A

Carcinoid tumor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
406
Q

Most common primary mediastinal neoplasm in adults

A

Hodgkin or non hodgkin lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
407
Q

Most common subtype of non hodgkin lymphoma

A

Lymphoblastic lymphoma and diffuse large b-cell lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
408
Q

Most common benign mediastinal germ cell neoplasm

A

Teratoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
409
Q

Most common type of teratoma seen in the mediastinum

A

Cystic or mature teratoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
410
Q

Most common malignant germ cell neoplasm

A

Seminoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
411
Q

Most common source of metastasis to middle mediastinal nodes

A

Bronchogenic carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
412
Q

Most common structure in the hiatal hernia

A

Stomach

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
413
Q

Most common primary malignancies of thoracic spinal metastases

A

Bronchogenic, Breast or Renal cell carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
414
Q

Most common posterior mediastinal mass in patients with neurofibromatosis

A

Meningocele

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
415
Q

Most common cause of chronic sclerosing fibrosing mediastinitis

A

Granulomatous infection usually secondary to histoplasma capsulatum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
416
Q

Most common affected structure in chronic sclerosing mediastinitis

A

Superior vena cava

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
417
Q

Most common source of pneumomediastinum

A

Air from lungs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
418
Q

Most common causes of small hila

A
  • Atelectasis
  • Lung resection (portion)
  • Pulmonary artery hypoplasia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
419
Q

Most common form of pulmonary edema

A

Hydrostatic pulmonary edema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
420
Q

Most common finding in pulmonary embolism without infarction

A

Peripheral airspace opacities and linear atelectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
421
Q

Most important parasitic infections of humans worldwide

A

Schistosomiasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
422
Q

Most common organisms seen in HIV-infected patients

A

S. pneumoniae
S. aureus
H. influenzae
E. coli
P. aeruginosa

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
423
Q

Most common cause of pulmonary arterial hypertension

A

Increase in resistance to pulmonary blood flow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
424
Q

Most common radiographic finding of lymphoma

A

Solitary pulmonary nodule or focal airspace opacity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
425
Q

Most common site of granular cell tumor

A

Skin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
426
Q

Most common type of lung cancer

A

Adenocarcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
427
Q

Most common subtype of lung cancer in non-smokers

A

Adenocarcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
428
Q

Most common cause of SVC syndrome

A

Lung cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
429
Q

Most common primary tracheal neoplasm

A

Squamous cell carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
430
Q

Most common location of the tracheal neoplasm

A

Distal trachea , within 3 to 4 cm of the tracheal carina

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
431
Q

Most common type of thyroid malignancy to invade the trachea

A

Papillary and follicular carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
432
Q

Most common mediastinal malignancies to invade the lung

A

Esophageal CA
Lymphoma
Malignant Germ Cell Tumor
Any malignancy metastasizing to the mediastinal or hilar lymph nodes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
433
Q

Most common extrathoracic malignancies to produce lymphangitic carcinomatosis

A

Breast CA
Stomach
Pancreas
Prostate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
434
Q

Most common pattern of disease and pulmonary infection

A

Lobular or bronchopneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
435
Q

Most common cause of multifocal patchy airspace opacities

A

Bronchopneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
436
Q

Most common cause of atypical pneumonia

A

Mycoplasma pneumoniae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
437
Q

Most common organism (nontuberculous mycobacteria) responsible for pulmonary disease

A

Mycobacterium avium intracellulare or M.kansasii

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
438
Q

Most common viral pneumonia in adults

A

Influenza

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
439
Q

Most common lung manifestation of blastomycosis

A

Homogenous nonsegmental airspace opacification with propensity for upper lobes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
440
Q

Most common method of pleuropulmonary involvement of amoebiasis

A

Direct intrathoracic extension of infection from a hepatic abscess

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
441
Q

Most common complication of pneumonia

A

Parapneumonic effusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
442
Q

Most common cause of pneumonia in immunocompromised hosts

A

Bacteria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
443
Q

Most common AIDS defining opportunistic infection

A

PCP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
444
Q

Most common cause of irregularity of lung interfaces

A

UIP and Sarcoidosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
445
Q

Most common diseases associated with architectural distortion

A

Sarcoidosis and UIP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
446
Q

Most common radiographic finding of rheumatoid lung disease

A

Interstitial pneumonitis and fibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
447
Q

Most common pleural manifestation of rheumatoid disease

A

Pleuritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
448
Q

Most common manifestation of sjogren syndrome

A

Interstitial fibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
449
Q

Most common of the idiopathic interstitial pneumonia

A

Usual interstitial pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
450
Q

Most common presentation of opacities in sarcoidosis

A

Bilateral symmetric reticulonodular opacities

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
451
Q

Most common cause of pleural thickening

A

Pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
452
Q

Most common benign manifestation of asbestos exposure

A

Pleural plaques

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
453
Q

Most common location of pleural plaques in the parietal pleura

A

Over the diaphragm and lower posterolateral chest wall

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
454
Q

Most common benign neoplasm of the chest wall

A

Lipoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
455
Q

Most common non vascular cause of inferior rib notching

A

Multiple intercostal neurofibromas in neurofibromatosis type 1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
456
Q

Most common site of the bony thorax involved by monostatic fibrous dysplasia

A

Ribs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
457
Q

Most common benign neoplasm of the ribs in adults

A

Osteochondroma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
458
Q

Most common primary rib neoplasm

A

Chondrosarcoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
459
Q

Most common type of diaphragmatic hernia

A

Esophageal hiatal hernia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
460
Q

Most common subtype of congenital cystic adenomatoid malformation

A

Composed of one or several large cysts lined by respiratory epithelium with scattered mucous glands, smooth muscle, and elastic tissue in their walls

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
461
Q

Most common cause of extrinsic mass effect in focal tracheal disease

A

Tortuous or dilated aortic arch or bronchiole cephalic artery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
462
Q

Most common type of emphysema

A

Centrilobular emphysema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
463
Q

Most common etiologic factor of emphysema

A

Cigarette smoking

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
464
Q

Most common radiographic finding of constrictive bronchiolitis

A

Diffuse reticulonodular opacities with associated hyperinflation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
465
Q

Most common condition to produce a transitive pleural effusion

A

Congestive heart failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
466
Q

Most common cause of parapneumonic effusion and emphysema

A

Staphylococcus aureus and gram-negative pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
467
Q

Most common side affected by pleural effusion in esophageal perforation

A

Left side

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
468
Q

Most common intrathoracic manifestation of Rheumatoid Arthritis and is most frequently seen in male patients following the onset of joint disease

A

Pleural effusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
469
Q

Most common cause of pneumothorax

A

Trauma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
470
Q

Most common subtype of malignant mesothelioma

A

Epithelial

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
471
Q

Most common cause of chest wall abscesses

A

Staphylococcus aureus and mycobacterium tuberculosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
472
Q

Most common malignant soft tissue neoplasms of the chest wall in adults

A

Fibrosarcomas and liposarcomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
473
Q

Most common congenital anomalies of the ribs

A

Bony fusion and bifid ribs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
474
Q

Most common cause of bilateral inferior rib notching

A

Coarctation of the aorta distal to the origin of the left subclavian artery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
475
Q

Most common metastatic lesions to the ribs

A

Bronchogenic and breast carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
476
Q

Most common type of rib metastases in breast and prostate carcinoma

A

Sclerotic rib metastases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
477
Q

Most common primary malignancy associated with metastasis to the scapula

A

Bronchogenic and breast carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
478
Q

Most common site in the lung that is involved with bronchial atresia

A

Apicoposterior segment of the left upper lobe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
479
Q

Most common pulmonary symptoms of arteriovenous malformations (AVMs)

A

Hemoptysis and dyspnea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
480
Q

Most common cause of right heart failure

A

Left heart failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
481
Q

Most commonly involved ribs in rib notching

A

3rd to 8th ribs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
482
Q

Most common location of ventricular aneurysms (What chamber is asked)

A

Left ventricle, posteroinferior aspect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
483
Q

Most common cause of dilated cardiomyopathy

A

Ischemic cardiomyopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
484
Q

Most common form of cardiomyopathies

A

Dilated cardiomyopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
485
Q

Least frequent form of cardiomyopathy

A

Restrictive cardiomyopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
486
Q

Most common cause of pulmonary venous hypertension

A

Elevation of the left atrial pressure secondary to left ventricular failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
487
Q

Most common cause of mitral regurgitation

A

Mitral valve prolapse

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
488
Q

Most common bacterial etiology of bacterial endocarditis BEFORE

A

Streptococcus viridans

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
489
Q

Most common bacterial etiology of bacterial endocarditis now

A

Staphylococcus aureus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
490
Q

Most common fungal agent followed by aspergillus

A

Candida albicans

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
491
Q

Most common location of cardiac thrombi

A

Left atrium and left ventricle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
492
Q

Most common location of atrial thrombi

A

Left atrium, Posterior wall

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
493
Q

Most common benign type of cardiac tumor

A

Atrial myxoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
494
Q

Second most common benign cardiac tumor

A

Lipoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
495
Q

Most common malignant cardiac tumor

A

Metastatic tumors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
496
Q

Most common primary malignant cardiac tumor

A

Angiosarcoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
497
Q

Most common primary neoplasms to metastasize to the heart
“B.L.ack LYfes M.atter” (BLLM)

A

B-reast
L-ung
LY-mphoma
M-elanoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
498
Q

Most common abnormality of the pericardium

A

Pericardial effusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
499
Q

Most common cause of constrictive pericardial disease

A

Post-pericardiotomy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
500
Q

Most common location of pericardial cysts

A

Anterior Cardiophrenic angles, right more common than left

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
501
Q

Useful for diagnosing coronary ischemia and myocardial infarcts

A

Perfusion scans with thallium or new technetium agents

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
502
Q

“Cold spot” imaging : Rest perfusion agents
“Hot spot” imaging : technetium pyrophosphate

A

Myocardial infarction scanning

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
503
Q

Used for diagnosing and sizing myocardial infarction

A

Antimyosin antibody scans

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
504
Q

Used to examine wall motion and allow left ventricular ejection fraction calculations

A

ECG-gated myocardial blood pool studies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
505
Q

Evaluation and quantification of right-to-left cardiac shunts

A

Technetium macroaggregated albumin or microspheres

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
506
Q

Adds wall motion evaluation, ventricular volumes and ejection fraction

A

ECG-gated SPECT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
507
Q

Assess cardiac metabolism as well as perfusion , enhancing its ability to evaluate cardiomyopathies , ischemic , infarction , and “hibernating” or viable myocardium

A

PET

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
508
Q

Uses a nasogastric tube with a steerable beam that views the heart and aorta from close posterior position provided by the esophagus

A

Transesophageal echocardiography

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
509
Q

Produces a time motion study of cardiac structures

A

Returning echoes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
510
Q

Anterior structures are displayed at the top of the images; techniques in motion of the myocardium can be evaluated throughout the cardiac cycle

A

Transthoracic technique

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
511
Q

Produced by a narrow ultrasonic beam that is directed at cardiac structures and observed over time or is swept across an area of anatomy

A

M-mode echocardiograms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
512
Q

Useful in evaluating aortic aneurysms, aortic dissections, injuries, vascular anomalies, central pulmonary emboli, into cardiac muscles, thrombi, pericardial thickening, fluid collections, and pericardial calcifications.

A

Cardiac MDCT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
513
Q

Provide functional information including wall motion analysis , systolic wall thickening , chamber volumes , stroke volumes , and right and left ventricular ejection fractions , and valvular evaluation

A

Cardiac MR

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
514
Q

Allow prior assessment of resting wall motion abnormalities that are consistent with either profoundly ischemic , stunned, hibernating , or infarcted myocardium

A

Stress echocardiography

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
515
Q

Evaluate the percent of stenosis , number of vessels involved , focal vs diffuse disease , coronary anatomy , ectasia or aneurysm , coronary calcification , and collateral flow

A

Coronary angiograms and CT coronary angiograms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
516
Q

Useful in detecting some of the long-term complications of ischemic disease including ventricular aneurysm , thinning of myocardium , akinesia , or dyskinesia

A

Echocardiography

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
517
Q

Capable of establishing the patency of CABG

A

CT coronary angiography

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
518
Q

Most accurate at detecting pseudoaneurysms

A

MRI

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
519
Q

Used to identify cardiac masses

A

CT, Angiography, and Nuclear scintigraphy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
520
Q

Initial mode for evaluation of cardiac masses

A

Echocardiography

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
521
Q

Used to differentiate tumor versus blood clot

A

MRI using gradient echo techniques

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
522
Q

Useful in determining the morphology of cardiac masses

A

MRI Gradient echo

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
523
Q

Excellent for detecting intracardiac tumors and evaluating direct intracardiac extension or pericardial involvement

A

MRI

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
524
Q

Useful in detecting loculated precardial effusions

A

CT scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
525
Q

Best imaging modality used to characterize pericardial fluid

A

MRI

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
526
Q

Boot-shaped heart appreciated in the plain chest x-ray PA view

A

Tetralogy of fallot

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
527
Q

Box shaped heart

A

Ebstein’s anomaly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
528
Q

Cardiac pathology with snowman configuration or snow man sign on CXR PA view

A

Total anomalous pulmonary venous return type 1 (TAPVR 1)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
529
Q

Egg on its side or apple on a stem configuration on CHEST XRAY PA view

A

Transposition of the great arteries (TGA)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
530
Q

“Figure of 3” sign on chest x-ray and “reverse figure 3” on barium esophagogram

A

Juxtaductal coarctation of the aorta

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
531
Q

Diverticulum of Kommerel

A

Aberrant left subclavian artery (ALSA)
“KOMMER (Come here), ALSA (random name of a girl)”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
532
Q

Double density sign on the right side of cardiac silhouette is a sign of what chamber enlargement?

A

Left Atrium, Left Atrial enlargement

“doubLAE density” sign

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
533
Q

Tetralogy of fallot exhibits increased or decreased pulmonary vascularity?

A

Decreased pulmonary vascularity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
534
Q

A.k.a the Vascular sling. Arises from right PA (posterior aspect) to reach the left lung and crosses mediastinum. A variant of this anomaly is “Ring-Sling” complex - stenosis of right bronchus and hypoplasia of the right lung, “Bridging bronchus”

“ALPA males use SLINGS with RINGS to cross BRIDGES in the BRONX for MEDIA coverage”

A

Aberrant left pulmonary artery (ALPA)
SLING = Vascular SLING
RING = RING-SLING complex
BRIDGE-ing BRONX-us
MEDIA-stinum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
535
Q

“Atrial escape” and “Walking man sign” pertain to enlargement of what structure?

A

Left atrium

“The Walking Man Left the Atrium to Escape”
Walking man sign, Left Atrium, Atrial escape

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
536
Q

“Hoffman-Riggler sign” pertains to enlargement of what structure?

A

Left ventricle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
537
Q

Enlargement of the pulmonary outflow tract is an indirect sign of the enlargement of which cardiac chamber?

A

Right ventricle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
538
Q

Most common cardiac tumor in the neonate and young infant

A

Rhabdomyoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
539
Q

Most common cause of pulmonary venous hypertension

A

Left ventricular failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
540
Q

Given a radiograph with a small cardiac silhouette and decreased pulmonary blood flow, which should you consider first before anything else?

A

Hypovolemia, first before congenital causes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
541
Q

What is the most common intracardiac mass?

A

Thrombi

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
542
Q

Type of pulmonary stenosis commonly seen in Tetralogy of Fallot

A

Infundibular or subvalvular pulmonic stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
543
Q

This pericardial abnormality predisposes to strangulation of cardiac structures (mechanical impairment of cardiac function) and possibility of sudden death

A

Partial absence / agenesis of pericardium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
544
Q

Atrial septal defect will demonstrate increased or decreased pulmonary vascularity?

A

Increased pulmonary vascularity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
545
Q

Most common cause of cyanotic congenital heart disease beyond the first 30 days of life

A

Tetralogy of Fallot

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
546
Q

This cardiac anomaly exhibits a functional left-to-right shunt and an obligatory right-to-left shunt

A

Total anomalous pulmonary venous return type 1 (TAPVR 1)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
547
Q

Most commonly associated with a right-sided aorta in 30 to 35% of cases

A

Persistent Truncus Arteriosus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
548
Q

Most common cause of congestive heart failure in the first day or two of life

A

Hypoplastic left heart syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
549
Q

Aneurysm of the ductus arteriosus will produce an unusually large bulge in what location of the mediastinum on plain chest x-ray films

A

Left upper mediastinum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
550
Q

The most common vascular anomaly

A

Aberrant right subclavian artery (ARSA)

“most common sARSA is Mang Tomas”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
551
Q

Most cases of Valvular pulmonary stenosis will show increased, decreased or normal pulmonary vascularity?

A

Normal vascularity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
552
Q

The most important or critical component of tetralogy of Fallot

A

Pulmonary stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
553
Q

Periaortic hematoma is a direct or indirect sign of aortic injury?

A

Indirect sign

Direct signs:
- Abnormal contour of aorta
- Change in caliber of aorta
- Contrast extravasation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
554
Q

Double barrel aorta is seen in

A

Aortic dissection (Intimal flap, 2 lumens)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
555
Q

Most common primary pericardial tumor

A

Mesothelioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
556
Q

Most common etiology for renal artery occlusive disease

A

Atherosclerosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
557
Q

Anomalous left common carotid artery wall produce anterior or posterior tracheal compression?

A

Anterior tracheal compression

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
558
Q

Most common cause of descending thoracic aortic aneurysm

A

Atherosclerosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
559
Q

Causes of ascending thoracic aortic aneurysm

A
  • Marfan
  • Syphilitic
  • Cystic medial necrosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
560
Q

Most common cause of right heart failure

A

Left heart failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
561
Q

A “Wall to wall” heart is associated with which valvular pathology

A

Tricuspid regurgitation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
562
Q

The earliest radiographic sign of congestive heart failure

A

Cephalization of pulmonary blood flow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
563
Q

Known as the “malignant” coronary anomaly

A

Interarterial

From the base of the aorta and pulmonary artery, prone to constriction and sudden cardiac death

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
564
Q

Cardiac chamber most commonly involved in idiopathic cardiomyopathy

A

Left ventricle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
565
Q

“Swinging heart” is seen and what of normality

A

Pericardial effusion (A very large one, >500 mL)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
566
Q

A 50% reduction in the diameter of a coronary artery corresponds to how much reduction in its cross-sectional area

A

75%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
567
Q

Required minimum amount of fluid in the pericardial sac to be detected by plain film radiography

A

200 mL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
568
Q

Most important predisposing factor for aortic dissection

A

Atherosclerosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
569
Q

Congenital subclavian steal syndrome is seen in which vascular anomaly

A

Isolated left subclavian artery
I’L S-teal = I-solated L-eft S-ubclavian Steal syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
570
Q

Most common cause of dilated cardiomyopathy

A

Ischemia

Non-ischemic causes include:
- Alcoholism
- Diabetes
- Hypertension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
571
Q

Most common cause of renovascular hypertension in patients younger than 40 years old

A

Fibromuscular disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
572
Q

Most common cause of renovascular hypertension in adults

A

Atherosclerosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
573
Q

Most important indication for coronary ct angiography

A

To exclude presence of significant coronary artery disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
574
Q

Majority of thoracic aneurysms involve which segment of the aorta

A

Ascending aorta

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
575
Q

Among the types of total anomalous pulmonary venous return, which is most commonly associated with pulmonary venous hypertension and edema

A

Type III (3), Infracardiac/Infradiaphragmatic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
576
Q

Type of pulmonary stenosis that will demonstrate post-stenotic dilatation of the pulmonary artery

A

Valvular

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
577
Q

Primary malignancy which has the highest frequency of metastases to the heart

A

Melanoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
578
Q

The usual initial chest x-ray finding of a patient with a first episode of acute myocardial infarction

A

Normal in 50% of cases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
579
Q

This vascular anomaly produces a characteristic indentation of the posterior aspect of the trachea just above the carina and a corresponding indentation of the anterior wall of the barium filled esophagus

A

Aberrant left pulmonary artery (ALPA)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
580
Q

Transient hypertrophy of the interventricular septum in the subaortic region of the left ventricle occurs in

A

Diabetic cardiomyopathy of the neonate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
581
Q

This will demonstrate an almost globular enlargement of the cardiac silhouette with almost equal bulging to the right and left of the spine

A

Pericardial effusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
582
Q

Most common cause of asymmetric pulmonary edema

A

Gravitational

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
583
Q

In what vascular anomaly is a “Reverse S-shaped” indentation on the esophagus demonstrated in the barium esophagogram

A

Double aortic arch

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
584
Q

Most common course abnormality of the coronary arteries

A

Myocardial bridging

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
585
Q

Most common location of a TRUE left ventricular aneurysm as a complication of acute myocardial infarction

A

Anterolateral wall

“anTRUElateral wall” True aneurysm
P-osterior wall = P-seudoaneurysm, Retro in location

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
586
Q

Threshold of an abnormally thickened pericardium

A

Greater than or equal to 4 mm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
587
Q

Angiographic hallmark of Buerger disease

A

Corkscrew appearance of arteries and absence of atherosclerosis findings often at wrists and ankles

DIABETIC = Vascular calcifications involving arteries of all sizes
ATHEROSCLEROSIS = multifocal diffuse luminal irregularities
GIANT CELL ARTERITIS = smooth and long-segment narrowing of axillary and/or brachial arteries
POLYARTERITIS NODOSA = microaneurysms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
588
Q

Most common primary malignant cardiac tumor in children

A

Rhabdomyosarcoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
589
Q

Aortic valve stenosis with pressure gradient across the aortic valve greater than 25 mmHg

A

Mild stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
590
Q

Aortic valve stenosis with pressure gradient across the aortic valve greater than 40-50 mmHg. Mild, moderate, or severe?

A

Moderate stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
591
Q

Aortic valve stenosis with pressure gradient across the aortic valve greater than 80 mmHg

A

Severe stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
592
Q

Mitral stenosis with orifice less than 1.5 cm squared

A

Mild mitral stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
593
Q

Mitral stenosis with orifice less than 1.0 cm squared

A

Moderate mitral stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
594
Q

Mitral stenosis with orifice less than 0.5 cm squared. Mild, moderate, or severe?

A

Severe mitral stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
595
Q

Mean pulmonary artery pressure exceeding more than 35 mmHg

A

Pulmonary arterial hypertension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
596
Q

Chamber enlargement best confirmed by measuring the distance from the mid inferior border of the left main stem bronchus to the right lateral border of the left atrial density. Greater than 7 cm indicates enlargement of this chamber

A

Left atrial enlargement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
597
Q

Chamber enlargement described as a prominent bulge too far to the right of the spine more than 5.5 cm from midline. There is also elongation of this right chamber convexity to exceed 50% of the mediastinal cardiovascular shadow.

A

Right atrial enlargement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
598
Q

Cardiac chamber enlargement with the apex pointing downward on PA view

A

Left ventricular enlargement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
599
Q

This sign is exhibited when the left ventricle extends more than 1.8 cm posterior to the posterior border of the IVC, 2cm cephalad to the intersection of the left ventricle and IVC.

A

Hoffman-Rigler sign in Left ventricular enlargement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
600
Q

Chamber enlargement described as climbing more than one-third of the sternal length and fill too much of the retrosternal space.

A

Right ventricular enlargement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
601
Q

“Viking helmet sign” (cardio)

A

Hilar fullness in Pulmonary venous hypertension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
602
Q

“bat wing” or “butterfly” or “angel wing” configuration of opacities is seen in what

A

Alveolar edema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
603
Q

Failure of the structure and function of the right ventricle in the absence of left ventricular dysfunction. May occur as right heart failure resulting from a pulmonary disease.

A

Cor pulmonale

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
604
Q

Measurement of pericardial fat stripe indicative of pericardial thickening or effusion

A

Percardial stripe >2 to 3 mm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
605
Q

Radiolucency surrounding the heart and separated from the lung by a thin white line of pericardium.

A

Pneumopericardium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
606
Q

Indicates that the heart is in the right hemithorax. Apex of the heart lies to the right, with the long axis of the heart directed from left to right

A

Dextrocardia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
607
Q

This syndrome is a combination of situs inversus with dextrocardia, bronchiectasis, and sinusitis.
“KART IN D.B.S.oria”

A

Kartagener syndrome

KART-agener syndrome
IN - versus (Situs)
D-extrocardia
B-ronchiectasis
S-inusitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
608
Q

Heart is shifted toward the right hemithorax. Associated with hypoplastic right lung and increased incidence of congenital heart disease, particularly left to right shunts.

A

Dextroposition

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
609
Q

Means cardiac apex is to the right but stomach and aortic knob remain on the left. The LV remains on the left but lies anterior to the RV.

A

Dextroversion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
610
Q

Most common cause of sternal fractures

A

Usually from MVA, 50% with cardiac contusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
611
Q

Hyperpigmentation of sternum is associated with…
“D.E.C (Dao Eng Chai)”

A

D = Dao = Down syndrome (90% of patients)
E = Eng = Engdo = Endocardial cushion defect
C = Complete AV canal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
612
Q

Wavy restrosternal linear opacities are due to and associated with what vascular abnormality?

A
  • Dilated internal mammy arteries associated with Coarctation of the aorta
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
613
Q

Pectus excavatum is associated and with increased incidence of…

A
  • Mitral valve prolapse (MVP)
  • Marfan syndrome
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
614
Q

Barrel shaped chest with pectus carinatum is associated with…

A
  • VSD = ‘V’arrel shaped chest
  • Complete AV canal
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
615
Q

Scoliosis with “Shield chest” can be seen in…
“M.A.C.Adi”

A

“M.A.C.Adi.mia”
M = Marfan syndrome
A = Aortic valve disease
C = Coarctation of the aorta
Adi = Aortic Dissection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
616
Q

11 or fewer ribs is associated with…

A
  • Down syndrome
  • AV canal
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
617
Q

“Ribbon ribs” or bifurcated ribs and overcirculation pattern suggests…

A
  • Truncus arteriosus
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
618
Q

Rib notching and inferior rib sclerosis occurs with…

A
  • Coarctation of the aorta
  • Blalock-Tausigg procedure
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
619
Q

In perfusion scanning with thallium, areas that show hypoperfusion on stress images while filling in on rest images are indicative of…

A

Ischemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
620
Q

“cold spot” imaging uses what agents

A

Rest perfusion agents

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
621
Q

“hot spot” imaging uses what agent

A

Technetium pyrophosphate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
622
Q

Paradoxical septal motion of the interventricular septum on echocardiography may be seen in

A
  • Pericardial effusion
  • Cardiac tamponade
  • ASD
  • Pulmonary hypertension
  • Left bundle branch block
  • Septal ischemia
  • Asthma
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
623
Q

Dilatation of the aortic root in echocardiography may be seen in

A
  • Aortic stenosis
  • Aortic insufficiency
  • Aortic aneurysm
  • TOF
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
624
Q

Delayed closure of the anterior leaflet of the mitral valve on echocardiography may be suggestive of

A

MS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
625
Q

High frequency vibration of the anterior leaflet of the mitral valve on echocardiography is known as what phenomenon and is associated with what valvular problem?

A

Austin Flint phenomenon, AR

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
626
Q

E-F slope of the mitral valve that appears flattened and more squared off than the normal M-shape is suggestive of

A

Mitral stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
627
Q

E-F slope of Tricuspid valve that is DECREASED may be seen in

A

Tricuspid stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
628
Q

Echocardiography:
E-F slope of Tricuspid valve that is INCREASED may be seen in…
“T.A.E”

A

T = Tricuspid regurgitation
A = ASD
E = Ebstein anomaly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
629
Q

What percent reduction of cross-sectional area is required to cause a significant reduction in blood flow?

A

75%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
630
Q

In general, this percentage of cross-sectional narrowing is considered clinically significant and will demonstrate decreased perfusion on stress myocardial perfusion imaging

A

> 50%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
631
Q

Collateral flow develops when there is this percentage of coronary stenosis

A

> 85%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
632
Q

Coronary pathology most often seen in the right coronary artery (RCA) as a smooth transient narrowing. 1-2 mm distal to the catheter tip. Patients remain asymptomatic.

A

Catheter-induced spasm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
633
Q

Angina secondary to prolonged coronary spasm. IV ergonovine may be used in a provocative tests to incite this coronary pathology. It is usually treated medically.

A

Prinzmetal variant angina

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
634
Q

An inflammatory condition of the coronary arteries. Small to medium vessel vasculitis, predominantly in children. Predilection for coronary arteries. Present with fever, congestion of conjunctiva, reddening of lips and oral mucosa, strawberry tongue and swelling of cervical lymph nodes.

A

Kawasaki disease

“Kawasaki bikes, whether small to medium sized, are close to my heart”
Kawasaki disease, small to medium sized vessels, predilection for coronary arteries (close to my heart)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
635
Q

Normal variant which the coronary arteries penetrate and then emerge from the myocardium rather than running along the surface of the epicardium. Causes arterial constriction during systole which refers to normal flow during diastole.

A

Myocardial bridging

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
636
Q

Coronary artery bypass grafting uses what

A

Saphenous vein grafts or native internal mammary arteries

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
637
Q

This remains a significant problem of stent placement in up to 50% of cases to be occurring within the first six months.

A

Restenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
638
Q

With angioplasty, by balloon dilatation of the stenotic lesion, is considered successful when stenosis is reduced to less than what percentage of diameter narrowing

A

Less than 50%, <50%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
639
Q

Coronary angiography wall motion:
Diminished contractility or less systolic motion than normal

A

Hypokinesia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
640
Q

Coronary angiography wall motion:
No systolic wall motion

A

Akinesia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
641
Q

Coronary angiography wall motion:
Paradoxical wall motion during systole

A

Dyskinesia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
642
Q

Coronary angiography wall motion:
Delayed contractility

A

Tardikinesia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
643
Q

Coronary angiography wall motion:
Cardiac motion that is out of phase with the remainder of the myocardium

A

Asynchrony

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
644
Q

Ventricular aneurysms that are lined by thinned and scarred myocardium. Broad mouthed, localized outpouching that do not contract during systole. Typically located near the apex or anterolateral wall.

A

True ventricular aneurysm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
645
Q

Ventricular aneurysms that are focal contained ruptures. Often larger but have narrower ostia / narrow mouthed. Most commonly located at the posterior and anterior aspect of the left ventricle

A

Pseudoaneurysms

Pseudoaneurysms of ventricle = Posteroanterior
True ventricular aneurysms = anTRUElateral

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
646
Q

True or false:
Intramural thrombi may be seen in 50% of ventricular aneurysms

A

True

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
647
Q

Cardiac artery calcium screening - Agatson score of 0-10

A

Very low to low risk

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
648
Q

Cardiac artery calcium screening - Agatson score of 11 to 100

A

Moderate risk

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
649
Q

Cardiac artery calcium screening - Agatson score of >400

A

High risk

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
650
Q

Now known to be the leading cause of myocardial infarction

A

Vulnerable plaque development, sudden rupture, and thrombosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
651
Q

Indications for coronary angiography include:
“Pilot w/ Abnormal Stress during Unstable flight”

A
  • Angina refractory to medical therapy (Unstable angina)
  • High-risk occupations (Pilot)
  • Abnormal ECG or stress perfusion tests
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
652
Q

True or false:
Use of Internal mammary artery has better long-term results than saphenous vein grafts, and correlated with increased survival.

A

True

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
653
Q

What condition presents with systolic pressure <90 mmHg and typically associated with acute pulmonary edema

A

Cardiogenic shock

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
654
Q

Common especially after inferior wall infarcts, from either ischemia or injury to the AV nodal branch of the RCA

A

AV block

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
655
Q

This complication of myocardial infarction occurs 3 to 14 days after infarction with a high mortality rate approaching 100%. Chest radiograph shows acute cardiac enlargement secondary to leakage of blood into pericardium with acute pulmonary vascular engorgement and right sided cardiac enlargement because of left to right shunt. Pulmonary edema is NOT TYPICAL.

A

Myocardial rupture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
656
Q

Inferior infarcts are associated with which location of papillary rupture?

A

Posteromedial papillary rupture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
657
Q

Anterior infarcts are associated with which location of papillary rupture?

A

Anterolateral papillary rupture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
658
Q

This complication of myocardial infarction is suggested by an abrupt onset of mitral regurgitation with acute pulmonary edema on the radiograph. The left ventricle is only minimally enlarged whereas the left atrium is enlarged quickly.

A

Papillary muscle rupture

NOTE: Myocardial infarction is PRONE to RUPTURE. If presented with a case of infarct and sudden changes in radiograph such as pulmonary edema or enlargement of ventricles, think RUPTURE.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
659
Q

A.k.a post-myocardial infarction syndrome. Similar to postpericardiotomy syndrome, complicating cardiac surgery. Considered an autoimmune reaction. Responds well with anti-inflammatory medications

A

Dressler syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
660
Q

Dressler syndrome will present with:

A
  • Fever
  • Chest pain
  • Pericardial effusion & pericarditis
  • Pleural effusion & pleuritis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
661
Q

True or false:
On “cold spot” imaging, acute infarction can be distinguished from remote infarction.

A

False. It cannot be distinguised from each other.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
662
Q

Myocardium that may act like postinfarction scar but remains viable and may improve in function with revascularisation

A

Hibernating myocardium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
663
Q

Myocardium that describes post-ischemic, dysfunctional myocardium without complete necrosis which is potentially salvageable

A

Stunned myocardium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
664
Q

Dilated cardiomyopathy can also be caused by acute myocarditis, most commonly with the etiologic agent

A

Coxsackie virus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
665
Q

Cardiomyopathy with global cardiomegaly seen on chest radiograph

A

Dilated cardiomyopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
666
Q

Cardiomyopathy with normal sized heart and pulmonary congestion seen on chest radiograph

A

Restrictive cardiomyopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
667
Q

Cardiomyopathy with chest xrays that are normal in 50% and presents with LAE in 30% of cases (because of mitral regurgitation)

A

Hypertrophic cardiomyopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
668
Q

Now described as an acquired disorder in infants or adults and is called Arrhythmogenic right ventricular dysplasia (ARVD). Limited to the RV with dilatation of the RV chamber, marked thinning of the ventricular wall and abnormal RV wall motion. MRI may show fatty infiltration of anterior RV free wall (essentially diagnostic)

A

Uhl anomaly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
669
Q

Right ventricular failure secondary to pulmonary parenchymal or pulmonary arterial disease. End result is alveolar hypoxia. Chest x-ray will show normal sized heart or mild cardiomegaly or even a small heart. Symptoms include marked dyspnea and decrease exercise endurance out of proportion to pulmonary function tests.

A

Cor pulmonale

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
670
Q

This should be considered whenever the main pulmonary artery and left and right pulmonary arteries are enlarged. Signs of right atrial and ventricular enlargement or hypertrophy or often present. Systolic right ventricular and pulmonary arterial pressures >30 mmHg

A

Pulmonary arterial hypertension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
671
Q

Acyanotic lesions include

A

ASD, VSD, PDA, and PAPVR

Clue to Acyanotic lesions:
Most have the letter ‘D’ in their name excluding PAPVR. A good mnemonic is “Dont ‘cyanose (Acyanotic) = asD, vsD, pDa”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
672
Q

Cyanotic lesions include

A

TGA, TA (Truncus arteriosus), TAPVR, and Endocardial cushion defects

Clue to Cyanotic lesions:
Most have the letter ‘T’ in their name excluding endocardial cushion defect.
Tga, Ta, Tapvr.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
673
Q

Small heart with decreased pulmonary blood flow may be caused by:

A
  • Hypovolemia
  • Malnourishment
  • COPD
  • Addison
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
674
Q

Decreased pulmonary blood flow with an enlarged cardiac silhouette include:

A
  • Cardiomyopathy
  • Pericardial tamponade
  • Ebstein
  • Right to left shunts
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
675
Q

This valvular heart disease is usually caused by rheumatic heart disease in the adult with 50% of patients giving a history of rheumatic heart fever

A

Mitral stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
676
Q

The syndrome is a combination of mitral stenosis with a pre-existing atrial septal defect resulting in marked right-sided enlargement.

“Ms. SAD Lutembacher has Marked right sided enlargement”

A

Lutembacher syndrome

“MS. SAD Lutembacher (some random european-like surname) has Marked right sided enlargement”
- Mitral stenosis
- ASD
- Lutembacher syndrome
- Marked right sided enlargement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
677
Q

Classification of mitral stenosis with <1.5 cm2 area, Normal CXR, Left atrial pressures elevated only on exercise

A

Mild mitral stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
678
Q

Classification of mitral stenosis with <1.0 cm2 area, LAE, Pulmonary venous hypertension, Dyspnea ON EXERTION is common

A

Moderate mitral stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
679
Q

Classification of mitral stenosis with <0.5 cm2 area, marked left atrial enlargement, right ventricular enlargement, Kerly lines, Pulmonary edema and patients are often DYSPNEIC AT REST.

A

Severe mitral stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
680
Q

Mitral regurgitation with normal xray. Classified as mild, moderate, or severe?

A

Mild Mitral regurgitation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
681
Q

Mitral regurgitation on radiography showing atrial enlargement and pulmonary venous hypertension

A

Moderate mitral regurgitation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
682
Q

Mitral regurgitation classification (mild, moderate, severe) on radiography showing progressive left atrial enlargement, left ventricular enlargement, pulmonary venous hypertension, and pulmonary edema.

A

Severe mitral regurgitation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
683
Q

Mitral regurgitation on MRI - Regurgitant jet grading

Turbulent flow extending less than 1/3 the distance to the back wall. What is the grade?

A

Grade 1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
684
Q

Mitral regurgitation on MRI - Regurgitant jet grading

Turbulent flow extending less than 2/3 the distance to the back wall. What is the grade?

A

Grade 2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
685
Q

Mitral regurgitation on MRI - Regurgitant jet grading

Turbulent flow extending more than 2/3 the distance to the back wall. What is the grade?

A

Grade 3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
686
Q

A.k.a “Floppy valve” or Barlow syndrome. Autosomal dominant. More common with pectus excavatum and narrow AP diameters of the chest. “Honking type” murmur or midsystolic click murmur is characteristic. On echocardiogram, characteristic BULGING LEAFLETS (anterior or posterior) during midsystole when valve should remain closed.

A

Mitral valve prolapse
“Barlow’s Floppy, Honking, Bulging Prolapse”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
687
Q

Most common type of adult aortic valve stenosis, present in 95% of congenital aortic stenosis

A

Bicuspid aortic valve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
688
Q

Most common valvular heart disease

A

Aortic stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
689
Q

Most common cause of aortic stenosis

A

Degeneration of the aortic valve / Degenerative calcification of the aortic valve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
690
Q

Aortic stenosis with orifice of 13-14 mm and greater than 25 mmHg gradient (Mild, Moderate, Severe?)

A

Mild aortic stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
691
Q

Aortic stenosis with orifice of 8-12 mm and greater than 40-50 mmHg gradient

A

Moderate aortic stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
692
Q

Aortic stenosis with orifice of <8 mm and >100 mmHg gradient (mild, moderate, severe?)

A

Severe aortic stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
693
Q

Most common bacterial agent in bacterial endocarditis

A

Staphylococcus aureus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
694
Q

Radiographic sign for chronic pericardial effusions

A

Water bottle sign/configuration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
695
Q

Minimum amount of fluid for small pericardial effusion and imaging findings on radiographs

A

<100 mL, appear as anterior and posterior sonolucent region

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
696
Q

Moderate pericardial effusion

A

100-500 mL, sonolucent zone around the entire ventricle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
697
Q

Very large effusion

A

> 500 mL, extend beyond the field of view and may be associated with “swinging heart” inside the pericardium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
698
Q

Serous pericardial fluid on MRI

A

T1 Dark, Gradient echo Bright

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
699
Q

Complicated or hemorrhagic effusions on MRI

A

T1 Bright, Gradient echo Dark

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
700
Q

Refers to cardiac chamber compression by pericardial effusion under tension, compromising diastolic filling. Clinical exam shows distended jugular veins, distant heart sounds, pericardial rub. Chest radiograph shows rapid enlargement of cardiac silhouette with relatively normal vascularity. (+) pulsus paradoxus

A

Cardiac tamponade

Pulsus paradoxus is an exaggeration of the usual drop in systolic pressure greater than 10 mmhg during inspiration. It occurs as a paradoxical motion during right ventricular filling.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
701
Q

This condition is associated with a widely swinging cardiac silhouette on decubitus view.

A

Congenital absence of the pericardium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
702
Q

Pericardial disease that is associated with the heart shifted towards the left with a prominent bulge of the right ventricular outflow tract, main pulmonary artery, and left atrial appendage. Insinuation of the lung into antero-posterior window and beneath is characteristic

A

Complete absence of the pericardium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
703
Q

Associated conditions with congenital absence of the pericardium:
“VSD is Sequestering DiapHers during Brunch”

A

VSD = Ventricular septal defect
Sequestering = Sequestration
Diaphers = DIAP-hragmatic HER-nias
Brunch = Brunchogenic cysts (Bronchogenic cysts)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
704
Q

Type of cardiomyopathy

Ventricular wall - LV thin
Ventricular cavity - LV dilated
Contractility - Decreased
Compliance - Normal to decreased

A

Dilated cardiomyopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
705
Q

Type of cardiomyopathy

Ventricular wall - LV thick
Ventricular cavity - LV normal to decreased
Contractility - Increased
Compliance - Decreased

A

Hypertrophic cardiomyopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
706
Q

Type of cardiomyopathy

Ventricular wall - Normal
Ventricular cavity - Normal
Contractility - Normal to decreased
Compliance - Severely decreased

A

Restrictive cardiomyopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
707
Q

Type of cardiomyopathy

Ventricular wall - RV thin
Ventricular cavity - RV dilated
Contractility - Decreased
Compliance - Normal to decreased

A

Uhl anomaly (Limited to Right ventricle)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
708
Q

Which ventricle dilatation causes a clockwise rotation of the heart

A

Right ventricle

Clockwise direction is RIGHTward therefore, RIGHT ventricular dilatation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
709
Q

Which ventricle dilatation causes a counterclockwise rotation of the heart

A

Left ventricle

Counter-clockwise is LEFT therefore LEFT ventricular dilatation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
710
Q

Chamber enlargement producing a “droopy” or “saggy” appearance of the cardiac silhouette

A

Left ventricle

Droopy or sagging is like downward displacement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
711
Q

Specific chamber enlargement depends on the site of the shunt:
Level of great vessels

A

Pure LEFT side enlargement

712
Q

Specific chamber enlargement depends on the site of the shunt:
If the shunt is at the Ventricular level, what chambers will enlarge?

A

Predominantly LEFT side enlargement or BIVENTRICULAR enlargement

713
Q

Specific chamber enlargement depends on the site of the shunt:
Shunt is located at the Atrial level

A

RA & RV undergo enlargement
LEFT side is NOT INVOLVED

714
Q

Most common congenital heart defect

A

VSD

715
Q

Second most common congenital heart defect

A

ASD

716
Q

Most common type of ASD

A

Ostium Secundum

717
Q

Type of ASD that results from the absence or defect in the flap of tissue derived from the septum primum, which covers and closes the foramen ovale.

A

Ostium secundum

718
Q

Type of ASD that results from maldevelopment of the primitive endocardial cushions.

A

Ostium primum

Prim for Primitive endocardial cushions

719
Q

Form of Ostium Primum with:
- Common AV valve usually with five leaflets.
- LOW Atrial, HIGH ventricular defects
- Large communication of all four chambers (Cardiomegaly)
- Diastole: GOOSE NECK DEFORMITY of Left ventricular outflow tract
- Systole: MV appears bilobed, irregular, scalloped

A

Complete form of Ostium Primum

720
Q

Manifests the same as PDA. Communication between the pulmonary artery & aorta just above their valves. Lesions from failure of complete septation of the primitive truncus arteriosus. LA & LV enlargement, pulmo artery dilatation, increased pulmo vascularity and a prominent aorta is seen.

A

Aortopulmonary window

721
Q

Most common anatomic arrangement of coronary artery fistula

A

One of the coronary arteries communicating with a cardiac chamber or pulmonary artery

722
Q

Most common coronary artery involved in coronary artery fistula

A

Right coronary artery (RCA)

723
Q

If a coronary artery fistula affects the right ventricle, which chamber enlarges

A

RV alone enlarges

724
Q

If a coronary artery fistula affects the right atrium, which chamber enlarges

A

Both RA & RV enlarge

725
Q

Which type of total anomalous pulmonary venous return will demonstrate a “snowman sign” or “snowman” anomaly

A

TAPVR Type I (1)

726
Q

Most common type of total anomalous pulmonary venous return

A

TAPVR Type I (1)

727
Q

Second most common type of total anomalous pulmonary venous return

A

TAPVR Type II (2)

728
Q

Which types of total anomalous pulmonary venous return are supradiaphragmatic in insertion of the anomalous pulmonary vein

A

TAPVR Types I & II (1&2)

729
Q

Which type of total anomalous pulmonary venous return is infradiaphragmatic when it comes to insertion of the anomalous pulmonary vein

A

TAPVR Type III (3)

730
Q

Type of total anomalous pulmonary venous return where the anomalous pulmonary veins terminate at a supracardiac level

A

TAPVR Type I

731
Q

Type of total anomalous pulmonary venous return where the anomalous pulmonary veins connect at a cardiac level, which drain to the coronary sinus then to the right atrium.

A

TAPVR Type II

732
Q

Type of total anomalous pulmonary venous return where the anomalous pulmonary veins join into a common vertical descending vein behind the left atrium, passing through the esophageal hiatus of the diaphragm, then joining the portal system.

A

TAPVR Type III (3)

733
Q

This congenital heart disease is described when all systemic and pulmonary venous blood goes to the right atrium and nothing drains to the left atrium

A

TAPVR

734
Q

A right-to-left shunt is required for survival in these congenital heart anomalies

A

TAPVR, TGA

For TAPVR: PATENT FORAMEN OVALE or less commonly, an ASD, is needed for survival

For TGA:
- VSD
- ASD with PDA is needed for survival

735
Q

A right-to-left shunt that is required for survival in a patient with total anomalous pulmonary venous return

A
  • Large patent foramen ovale (more common)
  • ASD (less common)
736
Q

Type of patent truncus arteriosus that is now identified by the term “pulmonary atresia/agenesis with VSD and systemic collaterals”

A

Type IV

737
Q

Most common type of patent truncus arteriosus

A

Type I

Both the aorta and main pulmonary artery arise from a common trunk, “Near” normal position

738
Q

Type of patent truncus arteriosus wherein the pulmonary arteries arise separately from the posterior aspect of the trunk close to each other, or just above the valve.

A

Type 2

739
Q

Type of patent truncus arteriosus that is the least common, wherein the pulmonary arteries arise independently from either side of the trunk

A

Type 3

740
Q

Most common cyanotic congenital cardiac anomaly in the newborn period

A

Transposition of the great arteries/vessels (TGA/TGV)

741
Q

An isolated TGA is incompatible with life at birth without one of the following additional anomalies

A
  • VSD (most commonly associated)
  • PDA (unstable due to closure at birth)
  • ASD (uncommon)
  • PFO (Patent foramen ovale, unstable)
742
Q

Most commonly involved ventricle in Single Ventricle congenital cardiac anomaly

A

Underdevelopment of the RIGHT VENTRICLE

743
Q

Congenital cardiac anomaly described as “Coeur en Sabot”

A

Tetralogy of fallot

“Coeur en sabot” means Boot-shaped heart

744
Q

Components of Tetralogy of Fallot:
“V.a.P.O.R”

A

V = VSD
a = (some cases only) absence of pulmonary artery & pulmo valve, artery coarctations
P = Pulmonary stenosis
O = Overriding aorta
R = RVH

745
Q

Critical component of Tetralogy of Fallot hemodynamically

A

Pulmonary stenosis

  • Results in right ventricular hypertrophy
  • regulates the degree of R-L shunting and aortic overriding
746
Q

Hypoplastic right heart syndrome components

A
  • Tricuspid atresia and stenosis
  • Pulmonary atresia
  • Hypoplastic RV
747
Q

The bulge that has resulted in the so-called appearance of a squared or box shaped heart in Ebstein’s anomay results from

A

Elevated “residual” RV

748
Q

In this congenital cardiac anomaly, there is focal or complete absence of the right ventricle myocardium and the right ventricle becomes a thin-walled fiber elastic bag. Contracts poorly and impedes the emptying of blood from the right side of the heart. Tricuspid efficiency is also present. Cyanosis results from right to left shunting.

A

Uhl’s disease

749
Q

This cardiac anomaly will have angiocardiographical findings of a small bulbous or spherical right ventricle. On MRI, It will present as a lumenless, right ventricular muscle mass.

A

Hypoplasia of the right ventricle

750
Q

Infantile hypercalcemia syndrome a.k.a “William’s syndrome” presents with ELFin facies (Looks like an Elf). Which type of congenital valvular disease is associated with this?

A

Aortic stenosis (Supravalvular type)

751
Q

This valvular pathology results in systemic overload and hypertrophy of the LV and in severe cases, enlargement of the LA. “Firm” or “Well rounded” appearance of the left side of the heart on CXR PA view. Prominence of the ascending aorta and aortic knob also noted. What is likely the valvular pathology?

A

Aortic stenosis / Valvular aortic stenosis

752
Q

“Figure of 3” sign well-demarcated on CXR, Aortic knob is higher in appearance but shows NO PRESSURE GRADIENT across area of kinking

A

PSEUDOcoarctation of aorta

753
Q

True or False:
PDA is always present in the Preductal/Isthmic/Infantile type of Coarctation of Aorta.

A

True

754
Q

True or False:
VSD is also always present in the Preductal/Isthmic/Infantile type of Coarctation of Aorta

A

False. VSD is OFTEN present only. ASD is the only one that is ALWAYS present in this type of Coarctation.

755
Q

A variable length of the aortic arch is absent or atretic, and blood is delivered to the descending aorta through a PDA. Locations include distal to the subclavian artery, distal to the left common carotid artery, or between the left common carotid and innominate arteries.

A

Interrupted Aortic Arch

756
Q

Rare congenital anomaly with abnormal hemodynamics similar to congenital mitral stenosis. An extra chamber is present proximal to the left atrium, representing persistence of the common pulmonary vein and in which the pulmonary veins drain. Symptoms are similar to MS but differ in a way because there is ABSENCE of left atrial enlargement.

A

Cor triatriatum

757
Q

Most common type of dextrocardia

A

“Mirror image dextrocardia”

758
Q

Cardiac apex points to the right and there is complete inversion of the cardiac chambers. LA and LV become right sided and the RA and RV become left-sided. Normal anteroposterior chamber relationships.

A

Dextrocardia

759
Q

Extreme right-sided rotation of the heart. Cardiac chambers lose their normal anteroposterior relationships. Chamber inversion does not occur. RA and RV becomes more posterior but remain on the right. LA and LV become anterior but remain on the left.

A

Dextroversion

760
Q

Heart lies midline, halfway between normal levoposition and abnormal dextroposition and can be considered incompletely dextroverted. Apex points anteriorly.

A

Mesoversion

761
Q

Chamber of the heart that is most commonly affected in idiopathic cardiomyopathy

A

Left ventricle

762
Q

Most common PERICARDIAL tumor noted in childhood and especially in infancy is…

A

Pericardial teratoma

763
Q

Most common cause of arterial aneurysm in the pediatric age group

A

Mycotic aneurysm secondary to infection due to umbilical artery catheterization

764
Q

Imaging study used to document urinary tract stones

A

CT scan

765
Q

Imaging study used to confirm and identify the cause of ureteral obstruction

A

CT scan

766
Q

Imaging study for bowel ischemia and infection

A

Contrast-enhanced MDCT

767
Q

Imaging study for hemochromatosis

A

MRI

768
Q

Preferred SCREENING method for biliary obstruction

A

Ultrasound

769
Q

Imaging study that provides excellent visualization of the biliary tree

A

MRCP

770
Q

Imaging study used primarily to guide therapy such as stent placement for biliary strictures, stone extraction and sphincterotomy

A

ERCP

771
Q

Imaging study utilizing technetium-99m and is useful for showing patency of biliary-enteric anastomosis and for demonstrating bile leaks and fistulae

A

Radionuclide scanning

772
Q

Imaging study performed by using agents such as iopanic acid formerly used for oral cholecystectography

A

CT cholangiography

773
Q

Imaging study that provides the most comprehensive initial assessment for the pancreas

A

Contrast-enhanced MDCT

774
Q

Imaging study that is useful for follow-up specific abnormalities of the pancreas

A

Ultrasound

775
Q

Imaging study that provides accurate tumor staging for the pancreas

A

CT with IVC and CT angiography

776
Q

Imaging study that confirms functioning splenic tissue

A

Radionuclide scans

777
Q

Primary imaging modality of stage of lymphoma

A

CT scan

778
Q

Most common cause of pneumoperitoneum

A

Duodenal or gastric ulcer perforations

779
Q

Most common calcified lymph nodes in the abdomen

A

Mesenteric nodes

780
Q

Most common narrowed areas in ureter that trap calculi

A
  • Ureteropelvic junction
  • Pelvic brim
  • Ureterovesical junction
781
Q

Most common cause of toxic megacolon

A

Acute ulcerative colitis

782
Q

Most specific sign of strangulation obstruction

A

Lack of enhancement of the bowel wall

783
Q

Most common area where gallstone lodges in gallstone ileus

A

Distal ileum

784
Q

Most common location of colonic obstructions

A

Sigmoid colon

785
Q

Most common type of cecal volvulus

A

Twist and invert

786
Q

Most common cause of large bowel obstruction in elderly and bedridden patients

A

Fecal impaction

787
Q

Most common sarcoma of the retroperitoneum

A

Liposarcoma

788
Q

Most common site of abscess formation

A

Pelvis

789
Q

Most common GI malignancy associated with AIDS

A

Kaposi sarcoma

790
Q

Most common abnormality demonstrated by hepatic imaging

A

Fatty liver

791
Q

Most common cause of fatty liver

A

Alcoholic liver disease and Nonalcoholic fatty liver disease (NAFLD)

792
Q

Most common area/segment involved in focal fatty sparing in the liver

A

Segment IV (4)

793
Q

Most common locations of focal fat

A

Falciform ligament, gallbladder fossa, and porta hepatis

794
Q

Most common cause of Budd-Chiari syndrome in western countries

A

Coagulation disorders

795
Q

Most common cause of budd-chiari syndrome in asian countries

A

Membranous webs obstructing the hepatic veins and IVC

796
Q

Most common malignant masses in the liver

A

Metastases

797
Q

Most common primary malignancies to produce hypovascular metastases
“Hypovascular Colored P.L.U.G”

A

Colorectal
Prostate
Lung
Uroepithelial
Gastric carcinomas

798
Q

Most common benign liver neoplasm and second to metastasis as the most common cause of liver mass

A

Cavernous hemangioma

799
Q

Most common primary malignancy of the liver

A

Hepatocellular carcinoma

800
Q

Second most common benign liver tumor

A

Focal nodular hyperplasia

801
Q

Most common primary tumors associated with intraluminal biliary metastases

A

Colorectal cancers

802
Q

Second most common malignant hepatic tumor

A

Cholangiocarcinoma

803
Q

Most common cause of cholecystoduodenal fistula

A

Gallstone (a complication of)

804
Q

Most common cause of chronic pancreatitis

A

Alcohol abuse (70%) and stone disease (20%)

805
Q

Second most common digestive tract malignancy

A

Pancreatic adenocarcinoma

806
Q

Most common pancreatic cystic lesions

A

Pseudocysts

807
Q

Most common imaging appearance of serous cystadenomas

A

Honeycomb microcysts with innumerable small cysts (1-2mm)

808
Q

Most common location of mucinous cystic neoplasm of the pancreas

A

Pancreatic tail

809
Q

Most common location of intraductal papillary mucinous neoplasms in the pancreas

A

Uncinate process

810
Q

Most common malignant tumor involving the spleen

A

Lymphoma

811
Q

Most common cause of neurologic dysfunction of neuromuscular disorders

A

Cerebrovascular disease and stroke

812
Q

Most common type of hiatal hernia

A

Sliding hiatal hernia

813
Q

Most common type of paraesophageal hernia

A

Mixed compound hiatal hernia

814
Q

Most common location of the lateral pharyngeal diverticula

A

Tonsillar fossa and Thyrohyoid membrane

815
Q

Most common cause of esophageal ulceration

A

Reflux esophagitis

816
Q

Most common cause of infectious esophagitis

A

Candida albicans

817
Q

Least common part of the GI tract involved in tuberculosis

A

Esophagus

818
Q

Most common cause of esophageal stricture

A

Reflux esophagitis (GERD)

819
Q

Most common location of webs in the cervical esophagus

A

Distal to the cricopharyngeal impression

820
Q

Most common form of cancer in pharyngeal and esophageal carcinoma

A

Squamous cell carcinomas

821
Q

Most common benign neoplasm of the esophagus

A

Leiomyomas

822
Q

Most common site of involvement of primary GI lymphoma

A

Stomach

823
Q

Most common mesenchymal tumors to arise from the GI tract

A

Gastrointestinal stromal tumors (GIST)

824
Q

Most common form of gastritis

A

H. pylori gastritis

825
Q

Most common cause of thickened gastric folds

A

H.pylori gastritis

826
Q

Most common cause of phlegmonous gastritis

A

Alpha hemolytic streptococcus

827
Q

Most common location of varices in the stomach

A

Fundus

828
Q

Most common location for neoplasm in the stomach

A

Distal stomach

829
Q

Most common part of the duodenum associated with malignancy

A

Fourth portion of the duodenum

830
Q

Most frequent malignant tumor of the duodenum

A

Duodenal adenocarcinoma

831
Q

Most common primary tumors involved with metastases of duodenum

A

Breast, Lung and other GI malignancies

832
Q

Most common location of GIST in the duodenum

A

Second and third portion of the duodenum

833
Q

Second most common primary malignant tumor of the duodenum

A

Malignant GISTs

834
Q

Most common congenital anomaly of the pancreas

A

Annular pancreas

835
Q

Most common neoplasm of the small intestine

A

Carcinoid

836
Q

Most common bowel involved in lymphomas

A

Small bowel

837
Q

Most common site for extranodal origin of lymphomas

A

GI tract

838
Q

Most common site of implantation of metastases in the small bowel

A

Terminal ileum, cecum, and ascending colon

839
Q

Most common location of lipoma in the GI tract

A

Ileum

840
Q

Mostly common location of Peutz-Jeghers syndrome

A

Jejunum

841
Q

Most common location of juvenile GI polyposis

A

Colon

842
Q

Most common solid mesenteric mass

A

Lymphoma

843
Q

Most radiosensitive organ in the abdomen

A

Small bowel

844
Q

Most common location of small bowel diverticula

A

Jejunum along the mesenteric border

845
Q

Most common congenital anomaly of the GI tract

A

Meckel diverticulum

846
Q

Most common malignancy of the GI tract

A

Colorectal adenocarcinoma

847
Q

Most commonly involved bowel in radiation colitis

A

Rectosigmoid

848
Q

Most common location of fistulas in acute diverticulitis

A

Bladder, vagina, and skin

849
Q

Most common cause of acute abdomen

A

Acute appendicitis

850
Q

Most common tumor of the appendix

A

Carcinoid

851
Q

Most common location for carcinoid tumour accounting for 60% of all carcinoids

A

Appendix

852
Q

Most common cause of gastric outlet obstruction

A

Edema or spasm from ulcer

853
Q

Abdominal radiographic finding of adynamic ileus

A

Seen on abdominal radiographs as dilated small and large bowels with multiple air fluid levels on upright projection

854
Q

True or false:
Portal venous gas on radiograph may be described as branching tubular lucency/ies seen at the periphery of the liver

A

True.

855
Q

Most useful radiographic view to evaluate lesions in the distal esophagus

A

Double contrast Upright Left posterior oblique view (LPO view)

856
Q

A 40 year old female presented with chest pain and dysphagia. Esophagogram revealed intermittently absent peristalsis in the thoracic portion of the esophagus producing alternating areas of narrowing. What is the diagnosis?

A

Diffuse esophageal spasm

857
Q

What esophageal motility disorder presents as decreased or absent primary peristalsis in the mid to distal esophagus and not associated with non peristaltic contractions?

A

Gastroesophageal reflux (GERD)

858
Q

True or false:
In GERD, Double contrast esophagogram shows fine nodular or granular appearance in the distal third of the esophagus

A

True

859
Q

Most common submucosal mass of the esophagus

A

Leiomyoma

860
Q

A stricture is present in the mid portion of the esophagus and is often associated with hiatal hernia. The walls of the stricture are irregular, flat and stiffened. Metaplasia of the esophagus. Considered a precursor of esophageal adenocarcinoma.

A

Barrett’s esophagus

861
Q

True or false:
Gastrointestinal stromal tumor (GIST) has malignant potential.

A

True

862
Q

True or false:
Barrett’s esophagus is not associated with esophageal adenocarcinoma.

A

False. There is an association of malignant potential in Barrett’s esophagus such as esophageal adenocarcinoma.

863
Q

True or false:
Presence of mass effect is not a major CT criteria used in staging esophageal cancer.

A

True.

864
Q

A 50 year old man presented with dysphagia. Esophagogram shows a solitary outpouching in the right side of the distal esophagus. What is the diagnosis?

A

Epiphrenic diverticulum

865
Q

Most common site of esophageal perforation secondary to endoscopic procedures

A

Cervical esophagus

866
Q

True or false:
With esophageal traction type of diverticulum, it will appear as a solitary, triangular, or tented outpouching

A

True

867
Q

Narrowed tubular stomach with smooth contour but having decreased or absent mucosal folds that is predominantly seen in the gastric body of fundus in barium contrast study

A

Atrophic gastritis

868
Q

A flat round object was accidentally swallowed by a three year old boy and lodged in the esophagus would be oriented in what plane

A

Coronal

869
Q

What description of ulcer favors a malignant type

A

When viewed in profile, ulcers do not project beyond the expected gastric contour

870
Q

Type of polyp which has a malignant potential

A

Adenomatous polyps

871
Q

A 55 year old male with long history of NSAID intake presented with dyspepsia and epigastric pain. esophagogram revealed punctate collections of barium surrounded by radiolucent halos. Diagnosis?

A

Erosive gastritis

872
Q

A contrast CT scan feature suggestive of a benign gastric tumor

A

Uniform diffuse enhancement

873
Q

Most common incidental finding in the duodenum seen on upper GI studies

A

Diverticula

874
Q

Presence of intestinal wall pneumatosis and portal venous gas in patients with obstruction may be signs of…

A

Ischemia and infarction

875
Q

What is the most common cause of small bowel obstruction in Adults

A

Adhesions

876
Q

True or false:
Barium studies in gastric volvulus is useful in demonstrating gastric outlet obstruction.

A

True

877
Q

A major risk factor in the pathogenesis of gastric carcinoma

A

H.pylori infection

878
Q

True or false:
Gastric carcinoma can extend through regional lymphatics into the retroperitoneum causing ureteral obstruction.

A

True

879
Q

True or false:
Dysfunction of the small bowel muscles will result in irregular, distended, or nodular thickening of the bowel loops.

A

False. Infiltration by cells or non-fluid material (primary or secondary involvement of tumor) will result in irregular, distended, or nodal or thickening of the bowel loops.

880
Q

True or false:
Majority of the gastric lymphomas are non-hodgkin’s lymphoma

A

True.

881
Q

True or false:
Stomach is the most commonly involved portion in the gastrointestinal system in lymphoma.

A

True

882
Q

A barium study of a 10 year old male with colicky abdominal pain showed convoluted, long, linear filling defects in the distal ileum. What is the diagnosis?

A

Ascariasis

883
Q

What mesenteric lesion would present as “sandwich sign” on CT scan study?

A

Lymphoma

884
Q

Barium study of a 17 year old patient with abdominal pain and diarrhea showed thickened bowel wall folds in the distal ileum with alternating areas of normal and deep bowel ulcerations. What is the diagnosis?

A

Crohn disease

Think “Crown”. A crown has high and low areas like alternating areas of normal and deep bowel ulcerations

885
Q

Most common location of small bowel tuberculosis

A

Ileocecal area

886
Q

CT scan finding of a 10 year old boy with abdominal pain showed outpouching in the antimesenteric side of the distal ileum is indicative of what disease?

A

Meckel diverticulitis

887
Q

What is the radiographic manifestation of diabetic gastroparesis?

A

Absent gastric peristalsis and gastric dilatation

888
Q

True or false:
Crohn disease will demonstrate multifocal, symmetric pattern of mural enhancement.

A

False. Asymmetric pattern

889
Q

Conditions that cause an extrinsic impression on the duodenum:

A
  • Hypertrophy of the caudate lobe
  • Presence of mass in the right kidney
  • Presence of mass in the right side of the colon
890
Q

The most common gluten-related disorder and is a T-cell mediated autoimmune chronic gluten intolerance condition characterized by a loss of villi in the proximal small bowel, seen radiographically as decreased mucosal folds and increased thickened folds in the ileum with gastrointestinal malabsorption.

A

Celiac disease

891
Q

True or false:
A polyposis syndrome such as Cowden’s disease has a higher risk for developing breast and thyroid cancers

A

True

892
Q

This small bowel malignancy can cause aneurysmal dilatation of the bowel

A

Lymphoma

893
Q

CT scan findings of a 56 year old patient with abdominal pain showed annular constricting mass in the jejunum with associated asymmetric wall thickening of the involved bowel. What is the most likely diagnosis?

A

Adenocarcinoma

894
Q

Most common route of metastatic spread to the small bowel

A

Intraperitoneal

895
Q

What is the hallmark of mechanical bowel obstruction

A

Point of transition between dilated and non-dilated bowel loops

896
Q

True or false:
Decreased bowel wall enhancement on CT scan is highly specific for acute bowel ischemia

A

True

897
Q

Ultrasound findings in a 45 year old male revealed herniating structures in the inguinal region that are lateral to the inferior epigastric vessels. What is the diagnosis?

A

Indirect inguinal hernia

898
Q

What bowel segment commonly herniates in a left inguinal hernia?

A

Sigmoid colon

899
Q

On barium studies, what radiographic view is helpful to demonstrate anterior abdominal wall hernia?

A

Lateral upright view with valsalva maneuver

900
Q

What abdominal aortic branch is commonly involved in acute mesenteric ischemia?

A

Superior mesenteric artery

901
Q

What is the most important indication for CT colonography?

A

To screen colorectal carcinoma

902
Q

What condition results when a loop of small intestine, with part of its mesentery, invaginates into the lumen of a bowel segment distal to it?

A

Intussusception

903
Q

Most common location of colorectal carcinoma

A

Rectum

904
Q

True or false:
Ulcerative colitis will present with confluent shallow ulcerations, granular mucosa, and symmetric disease around the lumen

A

True

905
Q

Most frequent complication of colorectal carcinoma

A

Obstruction

906
Q

This disease entity in the right lower abdomen will appear as an incompressible tubular structure with an AP diameter of larger than 7(or >6) mm in ultrasound.

A

Appendicitis

907
Q

What condition is present if the CT scan findings is a tubular, cystic mass with a calcified wall in the right lower quadrant of the abdomen, adjacent to the cecum?

A

Mucocele of the appendix

908
Q

A patient with congestive heart failure presents with imaging findings of a swollen liver showing reflux of contrast material into the distended hepatic veins and inferior vena cava. What is the diagnosis?

A

Passive hepatic congestion

909
Q

What fatty liver disease manifests as a geographic pattern of increased echogenicity?

A

Focal fatty sparing

910
Q

A 40 year old female presents with a 2-cm well-defined hypodense mass in the periphery of the liver. Contrast-enhanced CT study shows homogeneous enhancement in early arterial phase and remains isodense with the portal vein in the portal venous phase. What is the diagnosis?

A

Focal nodular hyperplasia

911
Q

True or false:
Hepatocellular carcinoma is predisposed to invade the biliary ducts.

A

False. Hepatocellular carcinoma is predisposed to invade the portal vein.

912
Q

What primary carcinoma usually produces a bullseye or target type of hepatic metastases

A

Bronchogenic carcinoma

913
Q

This feature differentiates a focal fatty infiltration from a hepatic mass

A

Angular or interdigitating geometric margins

914
Q

Role of ultrasound imaging in hepatitis

A

It is done to ensure that there is no biliary obstruction as the cause of liver disease.

915
Q

True or false:
There is hepatofugal flow in advanced liver cirrhosis on doppler studies.

A

True

916
Q

True or false:
Ultrasound finding of stones within the biliary tree - Small stones layer in the dependent area with its anterior portion outlined by the bile producing a crescent sign

A

True

917
Q

A 12 year old female with abdominal pain and jaundice presented with a right upper quadrant cystic mass that appears continuous to the common bile duct. What is the diagnosis?

A

Choledochal cyst

918
Q

True or false:
Adenomyomatosis of the gallbladder may present as a small polypoid mass fixed to the gallbladder wall.

A

True

919
Q

Imaging findings of a 50 year old diabetic female patient with abdominal pain shows the presence of cholelithiasis, with the gallbladder wall exhibiting dirty shadowing that has an arc-like configuration. What is the diagnosis?

A

Emphysematous cholecystitis

920
Q

True or false:
Porcelain gallbladder has an associated risk of developing gallbladder carcinoma.

A

True

921
Q

The most common vascular complication after liver transplantation

A

Hepatic artery thrombosis

922
Q

Features of chronic pancreatitis:

A
  • Decreased volume of pancreatic tissue
  • Dilated pancreatic duct
  • Calcifications in the pancreatic body
923
Q

A favorable prognostic factor which may indicate surgical resectability of pancreatic carcinoma

A

Isolated mass with or without dilatation of the bile or pancreatic ducts

924
Q

A patient with vomiting and weight loss shows a plain radiographic finding of a “double bubble’ sign. On esophagogram, the distal aspect of the stomach is elongated and narrowed. What is the diagnosis?

A

Hypertrophic pyloric stenosis

925
Q

True or false:
Regarding tumors of the spleen on sonography, metastatic lesions appear as small hemorrhages.

A

True

926
Q

Characteristic finding of a small round fat containing mass with stranding of the adjacent colon. It is usually seen in the left lower quadrant.

A

Epiploic appendagitis

927
Q

Conventional radiograph diagnostic of ascites require at least how many mL of fluid to be present

A

500 mL

928
Q

Sign of ascites described as appearance of symmetric densities due to spilling out of the cul-de-sac on either side of the bladder

A

“Dog’s ears” sign

929
Q

Gelatinous ascites or “Jelly belly”. Results from rupture of appendiceal mucocele, intrapersonal spread of benign or mucinous cysts of the ovary, or mucinous adenocarcinoma of the colon or rectum. On x-ray, punctate or ring-like calcifications scattered throughout the peritoneal cavity. On CT scan, mottled densities, septations and calcifications within the fluid. On ultrasound, hypoechoic to strongly echogenic intraperitoneal nodules.

A

Pseudomyxoma peritonei

930
Q

Sign of pneumoperitoneum - Gas on both sides of the bowel wall

A

Rigler sign

931
Q

Sign of pneumoperitoneum - gas outlining the peritoneal cavity

A

“Football sign”

932
Q

Calcifications that are plaque-like and oval in configuration conforming to the size and shape of the gallbladder

A

Porcelain gallbladder

933
Q

Most common component of gallstones

A

Calcium bilirubinate

934
Q

Suspension of radiopaque crystals within the gallbladder bile

A

Milk of calcium bile

935
Q

“Rice grain” calcifications in muscles may be suggestive of…

A

Cysticercosis

“cystRICErcosis”

936
Q

Nodular or sheet-like peritoneal calcifications are most commonly from…

A
  • Peritoneal dialysis
  • Previous peritonitis
  • Peritoneal carcinomatosis
937
Q

Refers to a segment of intestine that becomes paralyzed & dilated as it lies next to an inflamed intraabdominal organ. Alerts one on the presence of an adjacent inflammatory process.

A

Sentinel loop

938
Q

This is a manifestation of fulminant colitis characterized by extreme relation of all or a portion of the colon. In this state, peristalsis is absent and the large bowel loses all stone and contractility. Bowel wall becomes like a “wet blotting paper” and the risk of perforation is extreme.

A

Toxic megacolon

939
Q

Term applied to necrotizing fasciitis of the perineum, perianal, and genital regions. Polymicrobial organisms cause rapid tissue destruction. On radiographs and CT scans, bubbles and streaks of gas are seen in affected soft tissues.

A

Fournier gangrene

940
Q

A strong radiographic evidence of small bowel obstruction where air fluid levels at different heights are seen within the same loop

A

“Dynamic air-fluid levels”

941
Q

A strong evidence of bowel obstruction wherein particulate feculent matter mixed with gas bubbles is seen within the small bowel

A

“Small bowel feces” sign

942
Q

Most characteristic sign of small-bowel obstruction on CT scan

A

“Step ladder” or “hairpin loops” of small bowel

943
Q

Most common type of intussusception

A

Ileocolic

944
Q

Second most common type of intussusception

A

IleoIleocolic

945
Q

Most common cause of intussusception in adults

A

GI malignancy (Colorectal cancer)

946
Q

“Coiled spring” appearance on barium studies

A

Intussusception

947
Q

A cause of bowel obstruction that presents with alternating hyperechoic and hypoechoic rings representing alternating mucosa, muscular wall, and mesenteric fat tissues in cross-section exhibit a “doughnut” configuration on ultrasound

A

Intussusception

948
Q

Rigler triad in gallstone ileus

A
  • Dilated small bowel loops
  • Air in the biliary tree or gallbladder (Pneumobilia)
  • Ectopic Gallstone
949
Q

Sigmoid volvulus - what sign is expressed when the apex of the distended sigmoid colon may extend cephalad to the transverse colon

A

Northern exposure sign

950
Q

Sigmoid volvulus - what sign is demonstrated when oblique lines are created by the orientation of the transition zones of obstruction

A

“X-marks the spot” sign

951
Q

Sigmoid volvulus - single narrowing point of transition corresponding to what sign on barium enema

A

Beak sign

952
Q

Coffee bean shaped loop of gas distended bowel having haustral markings, direct with its apex directed towards the left upper quadrant.

A

Cecal volvulus

(The term coffee-bean shaped bowel loop was mentioned in radiopedia that it could be used as a general term for closed-loop obstruction. In Brant, however, this is specifically written under the Cecal volvulus portion of the chapter. Answer with main reference or specialty books in mind)

953
Q

Clinical disorder of acute colonic distention with abdominal pain but without the presence of mechanical obstruction. Current theory is imbalance in autonomic innervation of the colon.

A

Colonic pseudoobstruction

954
Q

Poor enhancement of the bowel wall along its mesenteric border is evidence of…

A

Bowel Ischemia

955
Q

Poor or absent mucosal enhancement with thinning of the bowel wall is evidence of…

A

Bowel infarction

956
Q

In lymphoma, this sign refers to entrapment of mesenteric vessels by masses of enlarged lymph nodes in the mesentery

A

Sandwich sign

957
Q

In lymphoma, this sign refers to masses of retroperitoneal nodes that silhouette segments of the normal echogenic wall of the aorta.

A

Sonographic silhouette sign

958
Q

CT scan findings include nodular, irregular peritoneal and omental thickening and masses which merge to large plaques and cake-like thickening of the omentum. What is the disease and sign being described?

A

Peritoneal mesothelioma, “Omental cake” sign

959
Q

CT scan demonstrates tumor nodules on peritoneal surfaces. What is the disease and sign being described?

A

Peritoneal metastasis, “Omental cake” sign (Also seen in Peritoneal mesothelioma)

960
Q

Most common sarcoma of the retroperitoneum

A

Liposarcomas

961
Q

Abdominal wall hernia that is not reducible

A

Incarcerated hernia

962
Q

Abdominal wall hernia that is associated with bowel obstruction and bowel ischemia

A

Strangulation hernia

963
Q

Abdominal wall hernia that entraps only a portion of the bowel wall without compromising viability. Also known as parietal hernias.

A

Richter hernia

964
Q

Type of inguinal hernia that extends through the internal inguinal ring into the inguinal canal lateral to the inferior epigastric vessels

A

Indirect inguinal hernia

965
Q

Type of inguinal hernia that occurs medial to the inferior epigastric vessels directly into the inguinal canal

A

Direct inguinal hernia

966
Q

Abdominal wall hernia that is formed from complications of surgery with herniation through a surgical incision

A

Incisional hernia

967
Q

Abdominal wall hernia that occurs through defects in the lumbar musculature posterolaterally below the 12th rib and above the iliac crest

A

Lumbar hernia

968
Q

Abdominal hernia wall hernia that occurs in the lower abdominal wall lateral to the rectus abdominis and inferior to the umbilicus through a defect in the aponeurosis of the transversus abdominis and internal oblique muscles

A

Spigelian hernia

969
Q

What sign is exhibited when fatty liver is dark on CT scan and bright on Ultrasound?

A

“Flip-flop” sign

970
Q

Most common type of nodule in cirrhosis

A

Regenerative nodules

971
Q

Type of dysplastic nodules in cirrhosis:
- minimal atypia
- not premalignant
- no mitosis
- no arterial phase enhancement
- supplied by portal vein

A

Low-grade dysplastic nodules

  • also progress to high-grade nodules
972
Q

Type of dysplastic nodules in cirrhosis:
- moderate atypia
- occasional mitosis
- secrete AFP
- premalignant, not frankly malignant
- blood supply from hepatic artery
- show arterial phase enhancement

A

High-grade dysplastic nodules

973
Q

This liver pathology produces a characteristic “nodule within a nodule” appearance seen as a high signal focus within a low-intensity nodule. The high signal focus enhances avidly on arterial phase.

A

HCC (small)

974
Q

Signs of pharyngeal dysfunction:

Defined as entry of barium into the laryngeal vestibule without the passage below the vocal cords

A

Laryngeal penetration

975
Q

Signs of pharyngeal dysfunction:

Defined as barium passage below the vocal cords.

A

Aspiration

976
Q

Signs of pharyngeal dysfunction:

Occurs when the soft palate does not make a good seal against the posterior pharyngeal wall.

A

Nasal regurgitation

977
Q

Esophageal plaques that appear as longitudinally oriented linear or irregular discrete filling defects in white with intervening normal-appearing mucosa

A

Candida albicans (Infectious esophagitis, Candidiasis)

978
Q

Esophageal strictures are typically smoothly tapering with concentric narrowing

A

Benign structures

979
Q

Esophageal strictures that are abrupt, asymmetric, eccentric in location, with irregular nodular mucosa

A

Malignant strictures

980
Q

On barium studies, this may present as smooth, long-segment narrowing of the esophagus or a series of ring-like structures called “ringed esophagus”. Treatment is steroids.

A

Eosinophilic esophagitis

981
Q

A pathologic ring-like structure at the level of the b-ring caused by reflux esophagitis

A

Schiatski ring

982
Q

Most common radiographic pattern of esophageal carcinoma

A

Annular constricting lesion - appearing as an irregular ulcerated stricture

983
Q

Rupture of the esophageal wall as a result of forceful vomiting. Always in the left posterior wall near the left crus of the diaphragm.

A

Boerhaave syndrome

984
Q

Trauma to the esophagus by violent retching. Only involves the mucosa and not the full thickness of the esophagus. On upper GI series, represents a longitudinally oriented barium collection 1-4 cm in length, in the distal esophagus

A

Mallory-Weiss tear

985
Q

Morphological growth pattern that can differentiate gastric carcinoma from lymphoma or vice versa

A

Gastric carcinoma = FOCAL plaque with central ulcer

Lymphoma = MULTIPLE submucosal nodules

But BOTH have growth patterns of:
- Polypoid mass
- Ulcerative mass
- Diffuse infiltration

986
Q

This term is used to describe diffuse gastric mucosal involvement of adenocarcinoma leading to THICKNESS and RIGIDITY of the stomach. It may be likened to the appearance of a “water bottle” stomach.

A

Linitis plastica

987
Q

Defects in the gastric mucosa that do not penetrate beyond the muscularis mucosae. These heal WITHOUT SCARRING.

A

Erosions

988
Q

Complete erosions of the gastric mucosa and appear as tiny central flock of barium surrounded by radiolucent halo of edema on barium studies.

A

Aphthous ulcers

989
Q

Chronic autoimmune disease of the stomach that destroys fundic mucosa but SPARES ANTRAL mucosa. Upper GI series findings of decreased or absent folds in the fundus or in the body termed “Bald fundus”

A

Atrophic gastritis

990
Q

Acute, often fatal, bacterial infection of the stomach most commonly caused by alpha hemolytic streptococcus. Multiple abscesses are formed in the gastric wall and rugae are swollen.

A

Phlegmonous gastritis

991
Q

Form of phlegmonous gastritis caused by gas-producing organisms such as E.coli and Clostridium. Caused by caustic ingestion, surgery, trauma, or ischemia.

A

Emphysematous gastritis

992
Q

Characterized by diffuse infiltration of the stomach and small bowel by eosinophils. Any or all layers may be involved. When chronic, the gastric antrum is narrowed with nodular, “cobblestone” mucosal pattern.

A

Eosinophilic gastroenteritis

993
Q

A.k.a “Giant hypertrophic gastritis” characterized by excessive mucus production, giant rugal hypertrophy, hypoproteinemia and hyperchlorhydria. Upper GI series show markedly enlarged and tortuous but pliable folds in the fundus and body, especially along the greater curvature, with sparing of the antrum. Hypersecretion has diluted the barium and impaired mucosal coating.

A

Menetrier disease

994
Q

Ulcers with the following signs are considered benign or malignant?

  • Ulcer within the lumen of the stomach
  • Ulcer eccentrically located
  • Shallow ulcer
  • Width greater than depth
  • Nodular, Rolled, Irregular or shouldered edges
  • “Carmen meniscus sign”
A

Malignant ulcers

“Carmen meniscus sign” - large, flat based ulcers with heaped up edges that fold inward to trap a lens-shape collection that is convex towards the lumen.

995
Q

Ulcers with the following signs are considered benign or malignant?

  • Ulcer with smooth mound and tapering edges
  • Edematous ulcer collar with overhanging mucosal edge
  • Ulcer projecting beyond the expected lumen
  • Radiating folds extending into the crater
  • Depth greater than width
  • Hampton line
A

Benign ulcers

Hampton line = thin, sharp, lucent line that traverses the orifice of the ulcer

996
Q

The most common location of BENIGN pathologies or mass lesions among the segments of duodenum?

A

D1 or Duodenal bulb
B-ulb B-enign

997
Q

Bilobed “dumb-bell” shaped enhancing mass in the duodenum

A

Duodenal adenocarcinoma

D-umbbell D-uodenal adenocarcinoma

998
Q

Type of duodenal adenomas with a high incidence of malignant degeneration and characteristic “cauliflower” appearance on double contrast upper GI series.

A

Villous adenomas

999
Q

Most common solid mesenteric mass in lymphoma

A

Bulky adenopathy

1000
Q

Congenital, partial, or complete replica of the small bowel. Arise from the distal small bowel and may communicate with normal intestinal lumen at one or both ends or not at all

A

GI duplication cyst

1001
Q

Produces atrophy of the muscularis of the small bowel by the process of progressive collagen deposition resulting in flaccid and dilated bowel. “Hide-bound” appearance of thinned folds tethered together is produced by contraction of the longitudinal layer to a greater extent than the circular layer. Duodenum and Jejunum are more severely involved in the ileum.

A

Scleroderma

1002
Q

Mucosa becomes flattened and absorptive cells decrease in number, villi disappear but submucosa, muscular, and serosa remain normal. Radiographic findings include dilated small bowel, normal or thinned folds, decreased number of folds in the duodenum and jejunum and increased number of folds in the ileum.

A

Adult celiac disease

1003
Q

Most common submucosal tumor of the colon

A

Lipoma

1004
Q

Most susceptible bowel segments to ischemic colitis due to them being watershed areas

A

Splenic flexure & Descending colon

1005
Q

An acquired condition in which the mucosa and muscularis mucosae herniate through the muscularis propria of the colon wall producing a circular outpouching.

A

Colon diverticulosis

1006
Q

Major risk factor for diverticulosis

A

Low-residue diet

1007
Q

True or false:
The saccular outpouchings in colon diverticulosis lack all the elements of the normal colon wall

A

True

1008
Q

Ectasia and kinking of mucosal and submucosal veins of the colon wall. Maze of distorted, dilated vascular channels replaces the normal mucosal structures and is separated from the bowel lumen only with a layer of epithelium. On angiography, tangled vessels without an associated mass may be seen.

A

Angiodysplasia

Angio- = vessel
-Dysplasia = abnormal, disorderly, distorted, tangled

1009
Q

Modality of choice for adrenal metastases

A

CT scan

1010
Q

Diagnostic method of choice in angiomyolipoma

A

MDCT

1011
Q

Effective in localizing pheochromocytoma

A

Radionuclide 131

1012
Q

Used to determine the chemical composition of stones

A

Dual-energy CT scan

1013
Q

Excellent screening modality for determining the presence of urinary tract dilation

A

Ultrasound

1014
Q

Used for confirmation of vesicoureteral reflux

A

VCUG or Radionuclide Cystography

1015
Q

Demonstrates urethral abnormality

A

Retrograde urethrography (RUG) or Voiding Cystourography (VCUG)

1016
Q

Used to stage known bladder carcinoma

A

Cross-sectional imaging and cystoscopy

1017
Q

Determines nodal metastases in transitional cell carcinoma

A

Biopsy

1018
Q

What planes or views Improve the accuracy of staging transitional cell carcinoma on MRI?

A

Coronal and sagittal planes

1019
Q

Modality used to study the anterior male urethra

A

Retrograde urethrogram (RUG)

1020
Q

Demonstrate the distention of both the posterior and anterior urethra

A

Voiding cystourethrography (VCUG)

1021
Q

Modality of choice for assessing the female urethra

A

Voiding cystourethrography (VCUG) or by retrograde urethrography (RUG)

1022
Q

Other modalities that may be used to image the female urethra aside from voiding cystourethrography (VCUG) or retrograde urethrogram (RUG)

A
  • Transrectal or perineal ultrasound
  • CT scan
1023
Q

Imaging method of choice for showing extent of carcinoma of the urethra

A

MRI

1024
Q

Primary modality for imaging of the female genital tract

A

Transvaginal or transabdominal ultrasound with Doppler techniques

1025
Q

Used to stage and follow-up pelvic malignancies and to supplement ultrasound by providing additional characterization of lesions

A

CT and MRI

1026
Q

Best for characterization of size, number, and location of leiomyomas

A

MRI

1027
Q

Best for the detection of adenomyosis

A

MRI

1028
Q

Most effective for the diagnosis of adnexal tumors

A

Ultrasound

1029
Q

Imaging used primarily for follow-up of known ovarian cancer

A

CT scan

1030
Q

Optimal imaging modality to determine the extent of cervical cancer and to demonstrate residual or recurrent tumor

A

PET CT scan

1031
Q

Used for initial evaluation of penile fracture

A

Ultrasound

1032
Q

Most accurate for imaging staging and for demonstrating adenopathy and tumor recurrence

A

MRI

1033
Q

Most common adrenal mass

A

Adrenal cortical adenoma

1034
Q

Most common primary tumors of adrenal metastases

A

Lung, breast, melanoma, gastrointestinal, thyroid, and renal

1035
Q

Most common cause of Addison disease in the U.S.

A

Idiopathic atrophy (probably autoimmune)

1036
Q

Most common adrenal tumor to hemorrhage spontaneously

A

Pheochromocytoma

1037
Q

Most common cause of adrenal hemorrhage in adults

A

Blunt trauma (80%) and infection

1038
Q

Most common calcified adrenal masses in adults

A

Adrenal pseudocysts, attributable to previous hemorrhage

1039
Q

Most common renal fusion anomaly

A

Horseshoe kidney

1040
Q

Most common appearance of renal abscess

A

Focal renal mass with thick wall

1041
Q

Most common cause of chronic pyelonephritis in children

A

Vesicoureteral reflux of infected urine

1042
Q

Most common component of staghorn calculi

A

Struvite stones (From Proteus mirabilis)

1043
Q

Most common cause of filling defects in the contrast-filled collecting system or ureter

A

Calculi / Stones

1044
Q

Second most common primary renal malignancy

A

Transitional cell carcinoma

1045
Q

Most common urinary tract neoplasm

A

Transitional cell carcinoma of the bladder

1046
Q

Most common location of Malakoplakia

A

Bladder

1047
Q

Most common stone in the urinary bladder

A

Solitary stones

1048
Q

Most common complication of urethral stricture

A

False passage

1049
Q

Most common site of urethral injury

A

Junction between prostatic and membranous urethra

(if not available in multiple choice, look for the words proximal urethra)

1050
Q

Most common site of saddle injury

A

Bulbous urethra

“Hit the Saddle and Get BOLDbous (hubad)”

1051
Q

Most common uterine tumor affecting 50% of women of reproductive age

A

Leiomyomas

1052
Q

Most common germ cell neoplasm of the ovary

A

Benign cystic teratoma

1053
Q

Most common gynecologic malignancy overall

A

Cervical cancer

1054
Q

Most common invasive gynecological malignancy

A

Endometrial cancer

1055
Q

Most common aggressive uterine malignancy

A

Uterine sarcoma

1056
Q

Most common cysts of the prostate

A

Cysts associated with benign prostatic hyperplasia

1057
Q

True or False:
Majority of adrenocortical adenomas
are non hyperfunctioning.

A

True

1058
Q

Most common cause of non-iatrogenic cushing syndrome

A

Adrenal hyperplasia

1059
Q

Most common cause of Conn syndrome

A

Adrenal cortical adenoma / Incidentaloma

1060
Q

“Rule of tens” of pheochromocytoma

A

10% Bilateral
10% Malignant
10% Incidental
10% Familial
10% Extra-adrenal

1061
Q

Most common cause of adrenal calcifications in both adults and children

A

Previous adrenal hemorrhage

1062
Q

Most common histologic type of renal cell carcinoma

A

Clear cell carcinoma (80%)

1063
Q

Most common renal mass

A

Simple renal cysts

1064
Q

What is the Bosniak category?

Indeterminate lesions that may be benign or malignant and are usually treated surgically. Thick irregular calcifications, irregular margins, thick enhancing septae, areas of nodularity

A

Bosniak category 3

1065
Q

A cystic renal mass that is also called “adult cystic nephroma” or “mixed epithelial and stromal tumors (MEST)”. It is a cluster of multiple non-communicating cysts of varying sizes separated by connective tissue septations of varying thickness.

A

Multilocular cystic nephroma

M-ultilocular cystic nephroma
M-EST / M-ixed Epithelial and Stromal Tumore
M-ature/Adult cystic nephroma

1066
Q

An autosomal dominant renal disease that manifests clinically later in life. The renal parenchyma is replaced by multiple non-communicating cysts of varying sizes.

A

Autosomal dominant polycystic disease

1067
Q

Development of multiple cysts in kidneys of patients on long-term hemodialysis. Exceeds 90% in patients after 4 to 10 years of hemodialysis

A

Aquired uremic cystic kidney disease

Clue to answer:
Acquired = bec. of hemodialysis
Uremic = related to kidney failure, abnormal renal fxn, and indirectly related to hemodialysis

1068
Q

Most frequent site of extrapulmonary tuberculosis

A

Urinary tract

1069
Q

Also known as “Putty Kidney”, demonstrating CASEOUS NECROSIS mixed with calcifications in dilated calyces

A

Renal tuberculosis

Clue: CASEOUS necrosis is a type of necrosis most common with tuberculosis

1070
Q

Primary cause of renal failure in HIV infected patients

A

HIV nephropathy

1071
Q

Most common component of staghorn calculi

A

Struvite (Magnesium ammonium phosphate)

1072
Q

Stones that are radiolucent on conventional radiographs

A

Uric acid and Xanthine stones

1073
Q

Most common cause of acute flank pain

A

Calculus obstructing the ureter

1074
Q

Due to an aperistaltic segment of the lower ureter 5-40 mm in length causing functional obstruction which will lead to the dilatation of the proximal ureter.

A

Congenital megaureter

1075
Q

Most common cause of filling defects in the contrast-filled collecting system or ureter

A

Calculi

1076
Q

Most common of all uroepithelial tumors

A

Transitional cell carcinoma (85-90%)

1077
Q

Squamous metaplasia with keratinization and desquamation results in irregular plaques in the renal pelvis, proximal ureter, and bladder. Key feature is the passage of flakes of discriminated epithelium in the urine. Considered as premalignant condition in the bladder but NOT in the ureter

A

Leukoplakia

1078
Q

Uroepithelium-lined cavities in the renal parenchyma that communicates through a narrow channel with a fornix of a nearby calyx. Can be congenital, developing from a ureteral bud remnant or acquired, because of infection, reflux, or rupture

A

Calyceal diverticuli

1079
Q

This bladder anomaly comes from congenital deficiency in the development of the lower anterior abdominal wall. The bladder is open and its mucosa is continuous with skin. Epispadias and wide diastasis of the symphysis pubis are associated.

A

Bladder exstrophy

1080
Q

Persistent communication between the bladder and umbilicus causes a urine leak. Patients are asymptomatic until an obstructive lesion of the lower urinary tract opens to an obliterated urachus causing umbilical urinary fistula.

A

Patent urachus

Clue: The words ‘persistent communication’ leads you to think ‘Patent’

1081
Q

Blind ended dilatation to urachus at the umbilical cord end. This may cause persistent umbilical discharge. When imaging a tubular structure is seen in the midline abdominal wall extending from the umbilicus.

A

Umbilical-Urachus Sinus

1082
Q

Outpouching of the bladder in the anterior midline location of the urachus. It is seen in adults with bladder outlet obstruction.

A

Vesical-Urachal diverticulum

1083
Q

This develops if the urachus is closed at both ends but remains patent in the midline. On imaging, a fluid filled cyst is seen in the midline abdominal wall usually in the lower third region of the urachus

A

Urachal cyst

1084
Q

Enlargement projects into the base of the bladder uplifting the bladder trigone and causing “J-hooking” of the distal ureter

A

Benign prostatic hypertrophy

1085
Q

Type of cystitis characterized by multiple, fluid-filled submucosal cysts

A

Cystitis cystica

1086
Q

Type of cystitis that is progression of cystitis cystica with proliferation of mucus secreting glands in the lamina propria. Precursor of adenocarcinoma of the bladder.

A

Cystitis glandularis

1087
Q

Type of cystitis that is usually associated with chronic irritation from indwelling catheters. Grape-like cysts elevate mucosa

A

Bullous edema

1088
Q

Type of cystitis characterized by hemorrhage into the mucosa and submucosa. Caused by bacterial or adenovirus

A

Hemorrhagic cystitis

1089
Q

Type of cystitis with Infiltration of the bladder wall by eosinophils. Cause is uncertain. Wall is greatly thickened and nodular.

A

Eosinophilic cystitis

1090
Q

Type of cystitis with gas within the bladder wall. Associated with poorly controlled diabetes mellitus, bladder outlet obstruction and E.coli

A

Emphysematous cystitis

1091
Q

Weigert-Mayer rule

A

With complete ureteral duplication, the ureter draining the upper pole inserts inferior and medial to the normally placed ureter draining the lower pole.

Upper pole OBSTRUCTS
Lower pole REFLUXES (prone to reflux due to the ectopic ureter for upper pole obstructing/distorting the passage through the bladder wall)

1092
Q

Most inflammatory strictures are caused by what etiologic agent?

A

Gonorrhea

1093
Q

Most common complication of urethral stricture?

A

False passage

1094
Q

Most common carcinoma of the urethra?

A

Squamous cell carcinoma

1095
Q

Squamous cell carcinoma of the urethra most commonly involves which portion of the urethra, Anterior or Posterior?

A

Anterior urethra

1096
Q

Classification of posterior urethral injury:
Contusion without imaging findings

A

Type 1

1097
Q

Classification of posterior urethral injury:
Stretch injury with elongation of the urethra without extravasation

A

Type 2

1098
Q

Classification of posterior urethral injury:
Partial disruption with extravasation of contrast and opacification of the bladder

A

Type 3

1099
Q

Classification of posterior urethral injury:
Complete disruption of the urethra without of opacification of the bladder with urethral separation less than 2 cm

A

Type 4

1100
Q

Classification of posterior urethral injury:
Complete disruption of the urethra without opacification of the bladder with urethral separation more/greater than 2 cm

A

Type 5

1101
Q

Failure of complete fusion of the mullerian duct:
- two uteri
- two cervices
- two vaginas

A

Uterine didelphys

1102
Q

Failure of complete fusion of the mullerian duct:
- two uterine horns
- One or two cervices
- One vagina

A

Bicornuate uterus

1103
Q

Failure of complete fusion of the mullerian duct:
- Midline septum dividing the uterus into two cavities

A

Arcuate uterus

1104
Q

Most common cause of hydrosalpinx

A

Pelvic infection , Pelvic inflammatory disease

1105
Q

Adhesions from previous surgery or inflammatory process entrap the ovary within a fluid collection that extends into the peritoneal recesses. Imaging shows a fluid collection that includes the ovary extending to the recess, giving the collection an angled or pointed shape rather than spherical or oval shape.

A

Peritoneal inclusion cyst

1106
Q

Meigs Syndrome
“Meigs likes to F.A.P”

A

“Meigs likes to FAP!”
- Fibromas (ovarian)
- Ascites
- Pleural effusion

1107
Q

Gynecologic emergency resulting from twisting of the ovary, fallopian tube, or most commonly both structures’ blood supply.

A

Adnexal torsion

1108
Q

Signs of hemorrhagic infarction of the torsed adnexa

A
  • Marked wall thickening of the adnexal mass (>10mm)
  • Hemorrhage within the mass
  • Hemorrhage within the twisted tube
  • Hemoperitoneum
1109
Q

A metastatic tumor of stomach and colon to the ovary. A “signet ring” subtype of metastatic tumor to the ovary.

A

Krukenberg tumor

1110
Q

Features that favor multiple simple cysts versus polycystic kidney disease:

A
  • Normal renal function
  • No family history
  • No cysts in other organs
1111
Q

Provides the most comprehensive imaging characterization for female genital tract congenital anomalies

A

MRI

1112
Q

Best for detection and characterization of adenomyosis

A

MRI

1113
Q

Most commonly used to further characterize lesions shown on ultrasound and to assess whether they are amenable to hysteroscopic resection

A

Hysterosalpingogram (HSG)

1114
Q

Diagnostic imaging method of choice for acute scrotal pain

A

Ultrasound with doppler / Doppler ultrasound

1115
Q

Excellent method for initial tumor staging and follow-up of nonseminomatous tumors

A

CT & MRI

1116
Q

Ultrasound mode used to document visualized cardiac activity

A

M-mode ultrasound

1117
Q

More sensitive than ultrasound in demonstrating the muscle invasive disease seen as focal myometrial masses, dilated vessels, and areas of hemorrhage and necrosis

A

MRI

1118
Q

Confirmation of placenta previa

A

Transperineal ultrasound

1119
Q

Imaging method of choice for placenta accreta

A

MRI

1120
Q

This modality will present with arterial waveforms at the fetal heart rate in vessels supplying chorioangioma is diagnostic

A

Spectral doppler

1121
Q

Great assistance in clarifying the nature of the borders of an apparent well-circumscribed solid mass

A

Magnification compression views

1122
Q

Imaging of choice to detect a primary breast lesion

A

MRI

1123
Q

Most accurate in identifying silicone implant rupture in in localizing free silicon

A

MRI

1124
Q

Most effective MRI sequence which suppresses the fat signal

A

IR sequence

1125
Q

Used to investigate the cause of a spontaneous nipple discharge

A

Ductography

1126
Q

Signal on T1WI MRI suggestive of benign etiologies

A

Bright / High T1

1127
Q

Signal on T2 weighted imaging MRI for simple cysts

A

Bright / High T2

1128
Q

Signal on T2WI MRI for most invasive carcinomas

A

Low / Dark T2

1129
Q

Signal on T2WI MRI for medullary or mucinous carcinomas

A

Bright / High T2

1130
Q

Most common form of adenomyosis

A

Diffuse form

1131
Q

Most common cause of postmenopausal bleeding

A

Endometrial atrophy associated with a thin endometrium

1132
Q

Most common symptom of submucosal leiomyomas

A

Bleeding throughout the menstrual cycle

1133
Q

Most common ovarian mass

A

Functional ovarian cyst

1134
Q

Most common ovarian neoplasm

A

Benign cystic teratoma / Dermoid

1135
Q

Most common primary tumors to metastasize in the ovary

A

GI and Breast

1136
Q

Most common causative agents of acute epididymo-orchitis

A

E.Coli, S. aureus, N.gonorrhea, and Tuberculosis

1137
Q

Most common primary testicular neoplasms

A

Germ cell tumor

1138
Q

Most common tumor still metastasize to the testes

A

Renal cell carcinoma (RCC) and Prostate carcinoma

1139
Q

Most common cause of painless scrotal swelling

A

Hydrocele

1140
Q

Most common correctable cause of male infertility

A

Varicocele

1141
Q

Most common location of ectopic pregnancy

A

Ampulla (70%) in the fallopian tube

1142
Q

Most common and most benign form of gestational trophoblastic disease

A

Hydatidiform mole

1143
Q

Most common solid pelvic masses encounter during pregnancy

A

Leiomyomas

1144
Q

Most common cystic pelvic masses found in pregnancy

A

Corpus luteal cyst

1145
Q

Single most common cause of a poor neonatal outcome

A

Cervical incompetence / Incompetent cervix

1146
Q

Most common tumor of the placenta

A

Chorioangioma

1147
Q

Most common chromosome abnormality increasing in incidence and currently occurring in 1 out of 500 births

A

Trisomy 21

1148
Q

Second most common chromosome abnormality

A

Trisomy 18

1149
Q

Most common neural tube defect

A

Anencephaly

1150
Q

Most common form of cleft lip and cleft palate

A

Lateral cleft

1151
Q

Most common causes of hydronephrosis in the fetus

A
  • Ureteropelvic junction obstruction
  • Ectopic ureterocele
  • Posterior urethral valves
1152
Q

Most common site of teratomas in fetus

A

Sacralcoccygeal region

1153
Q

Most commonly lethal skeletal dysplasia

A

Thanatophoric dwarfism

1154
Q

Most common location of breast abscess

A

Subareolar region

1155
Q

Most common well-circumscribed mass seen in women between ages of 35 to 50 years old

A

Cysts

1156
Q

Most common well-defined solid masses seen on mammography

A

Fibroadenomas

1157
Q

Most common primary cancer to produce breast metastasis

A

Melanoma

1158
Q

Most common indication for breast imaging in men

A

Palpable asymmetric thickening or mass

1159
Q

Most common presenting symptom of endometrial carcinoma

A

Postmenopausal bleeding

1160
Q

Modality used to better evaluate interstitial and airway abnormalities under certain conditions

A

HRCT

1161
Q

Modality used to verify diagnosis of central airway obstruction (tracheal obstruction)

A

Barium esophagogram

1162
Q

Definitive evaluation of the vascular anatomy is best accomplished by what modality

A

MRI or Helical CT scan

1163
Q

Valuable for distinguishing abscess from located empyema in the pleural space

A

CT scan

1164
Q

Most helpful to characterize chest wall masses

A

Ct scan

1165
Q

Used to evaluate for complications such as protrusion and migration

A

MDCT

1166
Q

Used to evaluate postoperative anatomy and in complications such as aortic regurgitation and pulmonary stenosis

A

MRI

1167
Q

Diagnostic modality used to detect single ventricle

A

Echocardiography

1168
Q

Evaluation of patients with TOF and other conotruncal anomalies after surgical repair; Assessing ventricular volumes and function of extra cardiac vascular anatomy and aorta pulmonary collaterals, evidence of valvular regurgitation, and regions of scarring

A

Cardiac MRI

1169
Q

Most reliable method to identify gastroesophageal reflux

A

24-hour esophageal pH and impedance monitoring

1170
Q

Preferred examination for hypertrophic pyloric stenosis

A

Ultrasound

1171
Q

Most commonly used to directly demonstrate obstruction in midgut volvulus

A

UGIS

1172
Q

Very effective and reliable imaging modality for Intussusception

A

Ultrasound

1173
Q

Study of viability of intestine

A

Doppler ultrasound

1174
Q

Used for the detection of abscess formation

A

Ultrasound or ct scan

1175
Q

Assess the adequacy of sphincter muscle complex; assess the position of the fistula and identify associated masses or GUT anomalies; post-operatively can establish that the pull through is properly positioned in relation to the sphincter

A

MRI

1176
Q

Primarily used to evaluate acute complications such as abscess, perforation, or post-surgical leaks

A

MDCT

1177
Q

Best modality for evaluation of perianal disease, fistulae, and abscesses

A

MRI

1178
Q

Best initial examination to identify a bleeding meckel’s diverticulum

A

Gadolinium MRI

1179
Q

Letter method of evaluating pyelonephritis and renal scarring; Ability to provide high-resolution anatomical detail as well as functional information about perfusion and contrast concentration and excretion of biopsy

A

MR Urography

1180
Q

More sensitive for vesicourereral reflux but provides poor anatomic detail

A

Nuclear scintigraphy

1181
Q

Provides better definition of urethra, bladder, and ureteropelvic anatomy

A

Voiding cystourethrography (VCUG)

1182
Q

Used to evaluate severity of hydronephrosis

A

Renal scintigraphy with furosemide wash-out

1183
Q

Distinguish autosomal dominant and recessive forms of polycystic kidney disease

A

High-resolution ultrasound technology

1184
Q

Ideal modality for adrenal hemorrhage

A

Ultrasound

1185
Q

Useful for classifying vaginal abnormality in older patients

A

MRI

1186
Q

Best defines a spinal origin of the mass and may associate tumor or spinal cord anomalies such as cord tethering

A

MRI

1187
Q

Most common cause of lobar pneumonia throughout childhood

A

Streptococcus pneumoniae

1188
Q

Most common bacterial infection that produces multiple bilateral alveolar opacities

A

Staphylococcal infection

1189
Q

Most common cause of an interstitial pattern in the lung of a child that is seen as hazy, reticular, or reticulonodular opacities

A

Viral or Mycoplasma infection

1190
Q

One of the most common causes of noncardiogenic causes of pulmonary edema predominantly in children

A

Acute glomerulonephritis

1191
Q

Most common cause of intrathoracic compression of the fetal lungs

A

Congenital diaphragmatic hernia

1192
Q

One of the most common causes of respiratory distress in the newborn

A

Surfactant deficiency disease (Hyaline membrane disease)

1193
Q

Most common cause of massive pleural effusion in the neonate

A

Chylothorax

1194
Q

Most common true lung masses

A

Postinflammatory granulomas or fungal infections

1195
Q

Most common malignant neoplasm in the lung during childhood

A

Metastases

1196
Q

Most common childhood tumors to metastasize to the lungs

A
  • Wilms tumor
  • Ewing sarcoma
  • Osteosarcoma
  • Rhabdomyosarcoma
1197
Q

Most common cause of an apparent anterior mediastinal mass

A

Thymus gland

1198
Q

Most common middle mediastinal mass

A

Lymphadenopathy

1199
Q

Most common malignancies to involve the chest wall in children

A

Ewing sarcoma and Primitive neuroectodermal tumor

1200
Q

Most common abnormality of the contour of the aorta

A

Coarctation of the aorta and dilatation of the aorta proximal and distal to the coarctation results in the characteristic “Figure of 3” sign

1201
Q

Most common congenital heart abnormality after bicuspid aortic valve

A

Ventricular septal defect (VSD)

1202
Q

Most common type of ventricular septal defect

A

Perimembranous defect

1203
Q

Most common type of atrial septal defect

A

Ostium secundum defect

1204
Q

Most common form of cyanotic congenital heart disease with increased pulmonary blood flow

A

Complete transposition of the great vessels (D-transposition)

1205
Q

Most common form of total anomalous pulmonary venous return (TAPVR)

A

Type 1

1206
Q

Most common anomaly to cause diminished pulmonary vascularity

A

Tetralogy of Fallot

1207
Q

Most common cause of cyanotic congenital heart disease

A

Tetralogy of Fallot

1208
Q

Most common inheritable cardiac disorder caused by genetic mutations that cause increased stress on myocytes and impaired function leading to hypertrophy and fibrosis

A

Hypertrophic cardiomyopathy

1209
Q

Most common type of cardiac malposition

A

Mirror-mirror dextrocardia

1210
Q

Most common congenital obstruction of the esophagus

A

Esophageal atresia

1211
Q

Most common cause of duodenal obstruction

A

Duodenal hematoma

1212
Q

Most common causes of distal small bowel obstruction in the neonate

A

Ileal atresia and meconium ileus

1213
Q

Most commonly involved in transient intussusception

A

Small bowel

1214
Q

Most common method for evaluating small bowel involvement

A

Contrast small-bowel fluoroscopic examination, Small intestinal series

1215
Q

Most common cystic lesion of the pancreas

A

Pancreatic pseudocyst

1216
Q

Most important causative factors of necrotizing enterocolitis

A

Ischemia and infection

1217
Q

Most common sites of urinary tract obstruction

A

Ureteropelvic junction, Ureterovesical junction, and pelvic brim

1218
Q

Most commonly urachal tumors

A

Adenocarcinoma

1219
Q

Most common cause of urethral obstruction in male infants

A

Posterior urethral valve

1220
Q

Most common cause of scrotal mass in children

A

Congenital hydrocele

1221
Q

Most common testicular neoplasm before puberty

A

Yolk sac tumor

1222
Q

Most common metastatic tumor to involve the testes in children

A

Leukemia and lymphoma

1223
Q

Most common abdominal masses in infants and children

A

Enlarged kidneys due to hydronephrosis

1224
Q

Most common renal neoplasm of childhood

A

Wilms tumor

1225
Q

Most common renal tumor of the neonate

A

Mesoblastic nephroma

1226
Q

Most common cause of adrenal enlargement in the newborn

A

Adrenal hemorrhage

1227
Q

Most common type of choledochal cyst

A

Type 1

1228
Q

Most common endocrine tumor

A

Insulinoma

1229
Q

Most common malignant tumor of the small intestine

A

Non-hodgkin lymphoma

1230
Q

Most common colon lesions

A

Inflammatory polyps or polyps associated with one of the colonic polyposis syndromes

1231
Q

Most common ovarian neoplasm in children and adolescents

A

Germ cell tumor

1232
Q

Most common germ cell tumors in young patients and is benign

A

Mature cystic teratoma

1233
Q

Most common tumor to affect the lower urinary tract in children

A

Rhabdomyosarcoma

1234
Q

Most common tumor in the newborn infant in the sacralcoccygeal region

A

Sacrococcygeal teratoma

1235
Q

Most common pseudomass / pulmonary “mass” in children

A

Round/Spherical pneumonia

1236
Q

Picture frame vertebrae, “Bone within a bone”, Bone-in-bone

A

Paget disease

1237
Q

Fish-shaped vertebrae

A

Sickle cell anemia, Osteoporosis, Renal osteodystrophy, Thalassemia

1238
Q

Rugger jersey vertebrae

A

Hyperparathyroidism, Renal osteodystrophy

1239
Q

Sandwich vertebrae

A

Osteopetrosis

1240
Q

H-shaped vertebrae, Lincoln log

A

Sickle cell anemia

Sharp depression at the central portion of the endplate. Due to bone infarction

1241
Q

Ivory vertebrae

A

Lymphoma (Hodgkin), Metastasis (Breast & Prostate), Paget disease

1242
Q

True or False:
Left to Right shunts cause cyanosis at birth.

A

False. Patients born with Left to right shunts are acyanotic at birth.

L to R shunt = L is for Lets you breathe (Acyanotic)

R to L shunt = R is for Removes air (Cyanotic)

L to R shunts have ‘D’s in their abbreviations (vsD, asD, pDa)

R to L shunts have ‘T’s in their abbreviations (TOF, TAPVR, TGA, TA)

1243
Q

Condition similar to patent ductus arteriosus (PDA) both hemodynamically and radiographically. Results from a failure of complete division of the primitive truncus arteriosus which leaves a communication between the aorta and the pulmonary artery just above the valves.

A

Aortopulmonary window

1244
Q

Most common form of cyanotic congenital heart disease with increased pulmonary blood flow

A

Transposition of the great vessels (Complete/D-transposition)

1245
Q

Pulmonary veins empty into a common drain that is abnormally incorporated into the left atrium. Radiographic findings of cardiomyopathy include cardiomegaly that is generalized or predominantly left-sided.

A

Cor Triatriatum

1246
Q

Result of absence of ganglion cells, Auerbach and Meissner’s plexuses, of the distal colon and rectum leading to abnormal peristalsis and inability to effectively evacuate to colon. Rectum is always involved.

A

Hirschsprung disease

1247
Q

Findings of peptic esophagitis:

A
  • Thickening of the esophageal wall
  • Lack of normal peristalsis
  • Tertiary contractions in the esophagus
  • Ulcers that may be superficial or deep
1248
Q

Most important causative factors of necrotizing enterocolitis

A

Ischemia and infection

1249
Q

Pathognomonic finding of necrotizing enterocolitis

A

Pneumatosis intestinalis

1250
Q

Vasculitis of unknown etiology. It affects the skin, GIT, joints, and kidneys. Half of the cases present with crampy abdominal pain and intestinal bleeding. Abdominal symptoms may proceed the characteristic skin rash. On UTZ, there is circumferential echogenic thickening of the bowel wall. On CT scan, there are multiple areas of bowel wall thickening, mesenteric edema, and lymphadenopathy.

A

Henoch-Schonlein Purpura

1251
Q

Most common structural abnormality of the GIT

A

Meckel diverticulum

1252
Q

This results from fibrous degeneration of the vitelline duct at the distal ileum. Presents with painless and sometimes profuse rectal bleeding. It arises from the ileum approximately 60 cm from the ileocecal valve.

A

Meckel diverticulum

1253
Q

Meckel diverticulum: Rule of ‘2’s

A

2 y/o
2/3 ectopic mucosa
2 feet (60cm) from ileocecal valve
2 inches (5cml long
2% of the population

1254
Q

Most common cause of renal scarring in children, which occurs independently from vesicoureteral reflux.

A

Pyelonephritis

1255
Q

What grade of vesicoureteral reflux is limited to the ureter?

A

Grade I

1256
Q

What grade of vesicoureteral reflux causes mild dilatation of the ureter and renal collecting structures?

A

Grade III

1257
Q

What grade of vesicoureteral reflux causes severe hydronephrosis with marked tortuosity and dilatation of the ureter?

A

Grade V

1258
Q

What grades of vesicoureteral reflux resolve spontaneously?

A

Grades I through III

1259
Q

What grades of vesicoureteral reflux are prone to scarring?

A

Grades III or higher

1260
Q

What grades of vesicoureteral reflux require surgery such as reimplantation of the ureter?

A

Grades IV and V

1261
Q

What type of posterior urethral valve results from abnormal migration and insertion of the urethrovaginal folds resulting in sail-like flaps of tissue that arise at the base of the prostatic urethra below the veromontanum.

A

Type I

1262
Q

What type of posterior urethral valve is caused by incomplete canalization in the region of the urogenital diaphragm?

A

Type III

1263
Q

What type of posterior urethral valve consists of a non-obstructive mucosal fold rather than an obstructing membrane?

A

Type II

1264
Q

Type of choledochal cyst with multiple dilatations / cysts involving the INTRAHEPATIC DUCTS ONLY.

Numerous intrahepatic cystic dilatations throughout the biliary tree and liver.

A

Type 5, Caroli disease

1265
Q

Type of choledochal cyst in which there is dilatation of an extrahepatic bile duct within the DUODENAL WALL or termed as CHOLEDOCHOCELE, at the ampulla of Vater region.

A

Type 3

1266
Q

Type of choledochal cyst which is considered a TRUE DIVERTICULUM from an extrahepatic duct. A saccular diverticulum from the CBD

A

Type 2

1267
Q

Most common etiology of acquired hepatic cysts in infants and children

A

Infectious in origin

1268
Q

Most common benign liver tumor encountered in infancy

A

Hemangioblastoma

1269
Q

This gastrointestinal mass commonly arises from the small bowel or colon. Most are asymptomatic. Can act as a lead point for intussusception and volvulus. On ultrasound, has a characteristic two-layered wall, consisting of an inner echogenic mucosa and peripheral hypoechoic muscle.

A

Enteric duplication cyst

1270
Q

These develop when a portion of the thecal sac protrudes anteriorly into presacral space through a sacral defect.

A

Anterior sacral meningocele

1271
Q

Currarino Triad (Anterior sacral meningoceles)

A
  • Partial sacral agenesis
  • Anorectal stenosis
  • Presacral mass
1272
Q

Also known as “Sickle shaped sacrum” or “Hemisacral agenesis”. Unilateral, well-marginated, crescent-shaped defect in the lateral sacrum. It is pathognomonic for anterior sacral meningoceles. Expansion of the meningocele causes scalloping and lateral displacement of the sacral plate.

A

Scimitar Sacrum

1273
Q

Most common benign cystic lesions in the phalanges

A

Enchondroma

1274
Q

Most common bone lesion encountered by radiologists

A

Non-ossifying fibroma

1275
Q

Most common location of Non-ossifying fibroma

A

Knee

1276
Q

Most common presentation of myeloma

A

Diffuse permeative

1277
Q

Most common differential diagnosis of a lytic lesion in the epiphysis of a patient less than 30 years old

A

Infection

1278
Q

Most reliable plain film indicator for benign vs malignant lesions

A

Zone of transition

1279
Q

Most common primary malignant bone tumor

A

Osteosarcoma

1280
Q

One of the most common fractures of the forearm

A

Colles fracture

1281
Q

Most common shoulder dislocation

A

Anterior dislocation

1282
Q

Most common arthritide/arthritis

A

Osteoarthritis

1283
Q

Most common cause of osteoporosis

A

Senile osteoporosis or osteoporosis of aging

1284
Q

Most common cause of Osteomalacia

A

Renal Osteodystrophy

1285
Q

Most common presentation of renal osteodystrophy

A

Osteopenia

1286
Q

Most common cause of dwarfism

A

Achondroplasia

1287
Q

Most common location of rim rent

A

Anterior at the insertion of the supraspinatus

1288
Q

Most commonly seen cuff tear in mri

A

Rim rent

1289
Q

Most common location of osteochondral lesion

A

Knee

1290
Q

Second most common location of osteochondral lesion

A

Talar dome

1291
Q

Most commonly torn ankle ligament

A

Anterior talofibular ligament

1292
Q

Most common cause of a painful flatfoot

A

Tarsal coalition

1293
Q

Most commonly fractured carpal bone

A

Scaphoid

1294
Q

Second most commonly fractured carpal bone

A

Triquetrum

1295
Q

Most commonly fractured tarsal bone

A

Calcaneus

1296
Q

Benign Lytic Bone Lesions - FEGNOMASHIC

A

F - ibrous dysplasia
E - nchondroma
G - iant cell tumor
N - on ossifying fibroma
O - steoblastomq
M - etastatic diseases, Myeloma
A - neurysmal bone cyst
S - imple bone cyst
H - yperparathyroidism (Brown tumor)
I - nfection
C - hondroblastoma, Chondromyxoid

1297
Q

FEGNOMASHIC:
No periosteal reaction

A

Fibrous dysplasia

1298
Q

FEGNOMASHIC:
Older than age 40

A

Metastasis, Myeloma

1299
Q

FEGNOMASHIC:
Expansile, Younger than 30

A

Aneurysmal bone cyst

1300
Q

FEGNOMASHIC:
Central, Younger than 30

A

Solitary bone cyst

1301
Q

FEGNOMASHIC:
Calcification present (except in phalanges), Painless (No periostitis)

A

Enchondroma

1302
Q

FEGNOMASHIC:
Eccentric, Epiphyses closed, Abuts articular surface (in long bones), Well-defined with non-sclerotic margins (in long bones)

A

Giant cell tumor

1303
Q

FEGNOMASHIC:
Younger than 30, Painless (No periostitis)

A

Non-ossifying fibroma

1304
Q

FEGNOMASHIC:
Younger than 30, Epiphyseal

A

Chondroblastoma

1305
Q

Refers to a fistulous connection between the gallbladder and the duodenum. It is considered the most common type of enterobiliary fistulation

A

Cholecystoduodenal fistula

1306
Q

Giant Cell Tumor characteristics:
“C.A.E.N”

A
  • Closed epiphyses
  • Abuts Articular surface
  • Eccentric
  • Non-sclerotic margins
1307
Q

Most common type of fibrous dysplasia

A

Monostotic

1308
Q

Benign lytic bone lesion that can be wild looking, discrete lucency, patchy, sclerotic, expansile, or multiple. Will not have periostitis. Never undergoes malignant degeneration. Should not be painful unless fractured.

A

Fibrous dysplasia

1309
Q

Benign lytic bone lesion with classic description of ground glass or smoky matrix. Often purely lytic and becomes hazy or takes on a ground glass look as the matrix calcifies.

A

Fibrous dysplasia

1310
Q

When this lesion is encountered in the tibia, it resembles fibrous dysplasia. It is a malignant tumor that radiographically and histologically resembles fibrous dysplasia. Occurs almost exclusively in the tibia and a draw and is rare

A

Adamantimoma

1311
Q

This syndrome has polycystic fibrous dysplasia which occasionally occurs in association with cafe au lait spots on skin (dark pigmented, freckle like lesions) and precocious puberty. Also presents with Chuberism (physical appearance of a child with puffed out cheeks having an angelic look. Jaw lesions regress in adulthood.

A

McCune Albright Syndrome

1312
Q

Differential for Enchondroma:
- multiple enchondroma
- not hereditary
- does not undergo malignant degeneration

A

Ollier disease

1313
Q

Differential for Enchondroma:
- multiple enchondroma with soft tissue hemangiomas
- not hereditary
- Undergoes malignant degeneration / Increased incidence

A

Maffucci syndrome

1314
Q

Benign lytic bone lesions that occurs in any bone formed from cartilage and maybe central, eccentric, expansile, or non expansile. Contain calcified chondroid matrix except in phalanges.

A

Enchondroma

1315
Q

Enchondroma versus Bone infarct: How to differentiate between the two?

A

Bone infarct = (-) endosteal scalloping
Enchondroma = (+) endosteal scalloping

1316
Q

A benign lytic bone lesions that have different phases of the same disease manifesting in one. Almost exclusively in patients less than 30 years old. Occasionally has a bony sequestrum. Can mimic Ewing sarcoma and perforated (multiple small holes) lesion.

A

Eosinophillic granuloma

1317
Q

True or False:
The rule that Giant Cell tumors abut the articular surface does not apply to FLAT BONES such as the pelvis or apophyses.

A

True. It does not apply to flat bones such as pelvis or apophyses which have no articular surfaces.

1318
Q

True or False:
If ANY of the four (4) criteria of Giant Cell Tumor are not met, it may be excluded from the differential diagnoses.

A

True.

1319
Q

Benign lytic bone lesion that occur in the metaphysis of a long bone emanating from the cortex. They are considered in patients less than 30 y/o that presents with no periostitis and no pain (asymptomatic). These lesions spontaneously regress and are rarely seen after 30 y/o. Also known as Fibroxanthoma. Most commonly seen in the KNEE but can occur in any long bone.

A

Non-ossifying fibroma

1320
Q

Benign lytic bone lesion that looks like a large osteoid osteoma and are often called “Giant Osteoid Osteomas”. They also simulate Aneurysmal bone cysts having a expansile, soap bubble appearance. If ABC is considered, so should this lesion. These commonly occur in the posterior elements of vertebral bodies and about half demonstrate speckled calcifications.

A

Osteoblastoma

1321
Q

This bone lesion spares some of the vertebral body (if involved) leaving struts of cortical bone giving the appearance of a “mini brain” on CT and MRI, which is pathognomonic for this.

A

Plasmacytoma

1322
Q

This benign lytic bone lesion most commonly presents as a diffuse permeative process in the skeleton. It can be solitary or multiple lytic lesions. On a lateral skull xray, it shows a typical presentation for this lesion as multiple, small holes throughout the calvarium which appear well-defined.

A

Myeloma / Multiple myeloma

1323
Q

True or False:
The only metastatic lesion that is said to always be lytic is renal cell carcinoma.

A

True.

1324
Q

True or False:
In general, lytic expansile metastatic diseases tend to come from thyroid and renal tumors.

A

True

1325
Q

Benign lytic bone lesion that virtually always expansile, occurs in <30 y/o, presence of fluid/fluid levels, (+) pain, and can be located anywhere in the skeleton. Primary type has no known cause or association with other lesions. Secondary type occurs in conjunction with another lesion or trauma.

A

Aneurysmal bone cyst

1326
Q

Benign lytic bone lesion that begins at the physeal plate and not at the epiphyses. It almost exclusively occurs in <30 y/o. Always central in location. Majority located in long bones such as proximal humerus and proximal femur. Fairly common location in the Calcaneus (inferior surface, almost exclusively). Asymptomatic unless fractured. “Fallen fragment” sign is pathognomonic.

A

Solitary bone cyst / Unicameral bone cyst

1327
Q

What sign is elicited when a piece of cortex breaks off after a fracture in a solitary bone cyst, and the piece of cortical bone sinks to the gravity-dependent portion of the lesion?

A

Fallen fragment sign

1328
Q

Benign lytic bone lesion that has subperiosteal bone resorption as a pathognomonic feature. Will present as frayed, ragged appearance of open physes, more commonly secondary to renal osteodystrophy (osteoporosis or osteosclerosis). Should be searched for in phalanges, distal clavicles, proximal tibias and sacroiliac joints.

A

Hyperparathyroidism / Brown tumors

1329
Q

Benign lytic bone lesion that has a protean appearance, may have sclerotic or non-sclerotic border, or have associated periostitis. If a bony sequestrum, this may be strongly considered. Soft tissue findings such as fat obliteration and cartilage loss or effusion are unreliable and misleading.

A

Osteomyelitis

1330
Q

A benign lytic lesion that only occurs adjacent to articular diseases such as a degenerative disease or arthritides. This lesion could be considered a…

A

Geode or subchondral cyst

1331
Q

Benign lytic bone lesions that resemble Non-ossifying fibromas (NOF), May occur at any age, (+) painful, (+) extend to metaphyses (whereas in NOFs, painless and do not extend to metaphyses). These are also cartilagenous lesions that DO NOT HAVE CALCIFIED MATRIX. Mentioned when an NOF is mentioned as primary impression.

A

Chondromyxoid fibroma

1332
Q

Benign lytic lesion seen in <30 y/o
“Younger people (<30) like S.N.A.C.I.Es” pronounced Snackies

A

S-olitary bone cysts
N-on ossifying fibroma
A-neurysmal bone cyst
C-hondroblastoma
I-nfection (Osteomyelitis)
E-osinophilic granuloma

1333
Q

Bone lesions that arise from Epiphyses:
“E.C.I.G.G” (pronounced as E-Cig as in electronic cigarettes)

A

E-piphyseal
C-hondroblastoma/C-hondrosarcoma
I-infection (Osteomyelitis)
G-iant cell tumor
G - eode / Subchondral cyst

1334
Q

Benign lytic bone lesions in patients older than 40:
“M&M Morbidity and Mortality”

A

M-etastasis
M-elanoma
(+) Infection / Osteomyelitis

1335
Q

Classic differential for benign, cystic RIB lesion:
“F.A.M.E.ous RIBS”

A

F-ibrous dysplasia
A-neurysmal bone cyst (ABC)
M-etastatic and M-yeloma
E-nchondroma

1336
Q

Multiply lytic bone lesions
“Multiple iEFEHM (iFM) radio stations”

A

i-nfection (Osteomyelitis)
E-nchondroma
F-ibrous dysplasia
E-osonophilic granuloma
H-yperparathyroidism (Brown tumor)
M-etastatic or M-yeloma

1337
Q

The only benign lytic bone lesion that must exhibit calcified matrix

A

Enchondroma

1338
Q

Benign lytic lesions that have NO PAIN OR PERIOSTITIS
“NO.F.EynS” pronounced as No Pains

A

N-on ossifying fibroma
F-ibrous dysplasia
Eyn-chondroma
S-olitary bone cyst

1339
Q

True or false:
Infection and eosinophilic granuloma cause aggressive periostitis and mimic a malignant tumor that can have a wide zone of transition.

A

True.

1340
Q

True or false:
A “permeative” zone of transition lesion consists of multiple small holes and has no perceptible border and therefore a wide zone of transition.

A

True

1341
Q

Examples of tumors that have “permeative” zone of transition (in general, Young or Old)

A
  • Multiple myeloma
  • Ewing sarcoma
  • Primary lymphoma of bone
1342
Q

Lipoma MRI signal

A

High T1 (due to fat content) and smooth/sharp margins

1343
Q

Hemangiomas and AVMs MRI signal

A

Mixed high and low signals on both sequences (fat and blood elements), characteristic LOW signal serpiginous vessels visible

1344
Q

True or false:
All solid tumors enhance with contrast MRI with the exception of myxoid or necrotic areas or foci of matrix (osteoid or cartilaginous)

A

True

1345
Q

“Sunburst” appearance of aggressive periosteal reaction occurs in…

A
  • Osteosarcoma (frequently)
  • Ewing sarcoma
  • Osteoblastic metastasis (prostate, lung, breast)
1346
Q

True or false:
Parosteal osteosarcoma occurs in an older age group than the central osteosarcomas and is not aggressive or as deadly as long as it has not extended into the medullary portion of the bone.

A

True.

1347
Q

True or false:
Ewing sarcoma exhibits onion-skin type of periostitis but can also have a periostitis that is sunburst or amorphous in character.

A

True.

1348
Q

Classic differential diagnosis for a permeative lesion in a child

A
  • Ewing sarcoma
  • Infection
  • Eosinophillic granuloma
1349
Q

Snowflake or popcorn-like, amorphous calcification seen in a long bone of a 43 y/o patient. (+) Pain

A

Chondrosarcoma

1350
Q

The only malignant tumor that can involve a large amount of bone or the patient is asymptomatic

A

Primary lymphoma of the bone

1351
Q

The only primary tumor that virtually never presents with blastic metastatic disease

A

Renal cell carcinoma (entirely lytic disease rather than blastic/sclerotic)

1352
Q

Typically has a diffuse permeative appearance that can mimic Ewing sarcoma or Primary lymphoma of the bone. Frequently involves the calvarium. One of the only lesions that is not characteristically “Hot” on a radionuclide bone scan. Bone or skeletal surveys are performed in place of a radionuclide bone scan.

A

Myeloma

1353
Q

True or false:
The diagnosis of Liposarcoma requires the presence of fat.

A

False. Liposarcoma might or might not have fat present. Lipoma, on the other hand, only requires visualization of fat on T1 to be determined.

1354
Q

True or false:
Synovial sarcomas only very rarely originated in a joint. They are often adjacent to joints.

A

True.

1355
Q

A benign joint lesion that occurs from metaplasia of the synovium that leads to multiple calcific loose bodies in a joint

A

Synovial osteochondromatosis

1356
Q

A benign synovial soft tissue process that causes joint swelling in pain and occasionally joint erosion. It virtually never has calcifications. Characteristic appearance on MRI is marked low signal lining the synovium seen on T1 and T2 because of the hemosiderin deposits.

A

Pigmented villonodular synovitis

1357
Q

Regarding bone lesions, what differentiates a true permeative pattern versus a pseudopermeative pattern?

A

Pseudopermeative pattern has INTACT CORTEX while a True permeative pattern occurs in intramedullary portion or the endosteal part of bone.

1358
Q

Atypical synovial cyst that is seen in the popliteal region at the knee joint that can present as a soft tissue mass. It is well-defined, fluid-filled, and homogenously hyperintense on T2 and often septated.

A

Baker cyst

1359
Q

A blow to the top of the head such as when an object falls directly on the apex of the skull can cause the lateral masses of C1 to slide apart splitting the bone ring of C1.

A

Jefferson fracture
“je-FIRST-son fx” First = C1 fracture

1360
Q

Atlantoaxial joint becomes fixed and the C1 & C2 bodies move together as one (en masse), instead of rotating on one another. Diagnosed with open mouth odontoid views. One of the spaces, lateral to the dens, is wider than the other and stays wider even with rotation of the head to the opposite side. Normally, with rotation of the head to the left, space on the left widens and vice versa.

A

Rotatory Fixation of the Atlantoaxial joint

1361
Q

Fracture of the C6 or C7 spinous processes

A

Clay shoveler fracture
“67ay shoveler” = C6 C7

1362
Q

Unstable serious fracture of the upper cervical spine that is caused by hyperextension and distraction (such as hitting one’s head on a dashboard). Fracture of the posterior elements of C2, usually displacement of the C2 body anterior to C3

A

Hangman fracture

“Hang | Man” (2 words = C2 fracture)

1363
Q

Severe flexion of the cervical spine can cause a disruption of the posterior ligaments with anterior compression of a vertebral body. Usually associated with spinal cord injury often from the posterior portion of the vertebral body being displaced into the central canal.

A

Flexion teardrop fracture

1364
Q

Severe flexion associated with some rotation can result in rupture of the apophyseal joint ligaments and facet joint dislocation. It can result in locking of the facets in an overriding position that causes some stabilization to protect against further injury. Occasionally occurs bilaterally.

A

Unilateral Locked Facets

1365
Q

Injury secondary to hyperflexion at the waist, as occurs in an automobile accident while restrained by a lap belt. Causes distraction of the posterior elements and ligaments and anterior compression of the vertebral body. This usually involves the T12, L1 and L2 level.

A

“Seatbelt injury”

seatbe12, seatbeL1, seatbeL2 (T12, L1, L2)

1366
Q

Also known as seatbelt fractures. These are flexion-distraction injuries of the spine that extend to involve all three spinal columns. These are unstable injuries and have a high association with intra-abdominal injuries such as pancreas and duodenum.

A

Chance fractures

1367
Q

Break or defect into pars interarticularis portion of the lamina

A

Spondylolysis

1368
Q

Scottie dog with collar sign

A

Spondylolysis

1369
Q

Denotes the slippage of one vertebra relative to the one below.Can occur anywhere in the vertebral column but is most frequent in the lumbar spine, particularly when due to spondylolysisat L5/S1.

A

Spondylolisthesis

spondylo-SLIP-thesis = Slippage

1370
Q

An eponymous name for osteonecrosisand collapse of a vertebral body. It represents delayed (usually two weeks) vertebral body collapse due to ischemia and non-union of anterior vertebral body wedge fractures after major trauma. Plain radiograph / CT scan shows collapse of affected vertebrae (typically lower thoracic and upper lumbar).

A

Kummel disease

1371
Q

Fracture at the base of the thumb/first digit into the carpometacarpal joint.

A

Bennet fracture

1372
Q

Commuted fracture of the base of the thumb/first digit that extends into the carpometacarpal joint

A

Rolando fracture

1373
Q

Fracture of the base of the thumb/first digit that does not involve the carpometacarpal joint

A

Pseudo-Bennett fracture

1374
Q

Avulsion injury at the base of the distal phalanx where the extensor digitorum tendon inserts

A

Mallet finger or Baseball finger

This is also like the injury related to basketball “Na-pingeran/fingeran”

1375
Q

Avulsion on the ulnar aspect of the first metacarpal phalangeal joint where the ulnar collateral ligament of the thumb inserts. It requires internal fixation. Usually occurs when falling on a ski pole and having the pole jam into the webbing between the thumb and the index finger.

A

Gamekeeper’s thumb

1376
Q

Occurs when the ligaments between the capitate and the lunate are disrupted allowing the capitate to dislocate from the cup-shaped articulation of lunate. Can also occur with fall on an outstretched arm. Normally, the capitated should be seen in the cup-shaped lunate.

A

Lunate / Perilunate dislocation

1377
Q

Failure to diagnose and treat lunate / perilunate dislocation will lead to permanent injury of what nerve?

A

Median nerve

1378
Q

True or false:
On AP view, Lunate/Perilunate dislocation will present as a rhomboid shape.

A

False. Lunate/Perilunate dislocation will present as triangular or pie-shaped lunate on AP view.

1379
Q

Most commonly associated fracture associated with Lunate / Perilunate dislocation

A

Transscaphoid/Scaphoid fracture

1380
Q

What view should you order when you want to see a fracture of the hook of hamate?

A

Carpal tunnel view

1381
Q

Most common cause of hook of the hamate fracture

A

Fall On Out-Stretched Hand (FOOSH)

1382
Q

Rotary subluxation of the Schapoid bone is another wrist injury after FOOSH. It results from rupture of the scapholunate ligament. What sign is demonstrated when there is space between the scaphoid and the lunate where ordinarily they are closely opposed?

A

Terry Thomas sign
“ro-TERRY subluxation of Scaphoid”

Named after a famous british actor (1950s) with a GAP BETWEEN HIS TWO FRONT TEETH

1383
Q

The eponymous name given to osteonecrosis involving the lunate. It is often referred to as lunatomalacia. Diagnosed by noting increased density of the lunate which may or may not go on to collapse and fragmentation.

A

Kienbock disease / Kienbock malacia

1384
Q

Type of ulnar variance if the Ulna is SHORTER than radius and is associated with increased incidence of Kienbock disease/ malacia.

A

Negative ulnar variance

1385
Q

Type of ulnar variance if the Ulna is LONGER than radius and is associated with increased incidence of Triangular fibrocartilage tears.

A

Positive ulnar variance

1386
Q

A small chip of the bone on the dorsal aspect of the wrist seen on lateral film is virtually pathognomonic of an avulsion from which carpal bone fracture?

A

Triquetrial fracture

1387
Q

Fracture of the distal radius and ulna after a fall on an outstretched arm/hand. Results in dorsal angulation of the distal forearm and wrist. Dinner fork deformity. Dorsally flexed FOOSH.

A

Colles fracture

“colle-D it!” pronounced Called it!
D-istal ra-D-ius
D-orsal angulation
D-istal forearm
D-inner fork deformity
D-orsally flexed FOOSH

1388
Q

Ulnar or long bones suffer a traumatic insult and force on the bones causes BENDING instead of a fracture. No visible fracture line or visible cortical injury noted. If left untreated, may result in reduced supination and pronation.

A

Plastic bowing deformity

1389
Q

Fracture of the ulna with dislocation of the proximal radius

A

Monteggia fracture

“MUGR” pronounced Mugger/Robber
M-onteggiA
U-lnar fracture
G-aleazzi
R-adial fracture

For dislocations, use this:
monteggiaA = A is proximal in the alphabet so PROXIMAL radial dislocation
galeaZZi = Z is distal in the alphabet so DISTAL ulnar dislocation

1390
Q

Fracture or the Radius with dislocation of the distal ulna

A

Galezzi fracture

“MUGR” pronounced Mugger/Robber
M-onteggiA
U-lnar fracture
G-aleazzi
R-adial fracture

For dislocations, use this:
monteggiaA = A is proximal in the alphabet so PROXIMAL radial dislocation
galeaZZi = Z is distal in the alphabet so DISTAL ulnar dislocation

1391
Q

A visible posterior fat pad sign of the elbow in an adult patient (closed epiphyses) is seen. This is indicative of what fracture?

A

Fracture of the radial head (elbow region)

1392
Q

A visible posterior fat pad sign of the elbow in a child (open epiphyses) is seen. This is indicative of what fracture?

A

Supracondylar fracture

1393
Q

True or false:
In the setting of trauma, a visible posterior fat pad sign is indicative of an elbow fracture.

A

True.

1394
Q

In elbow injury, effusion displaces the normally visible anterior fat pad superiorly and outward from the humerus and has been likened to the appearance of a spinnaker sail. This sign is called?

A

Sail sign

1395
Q

Occurs when the arm is forcibly external rotated and abducted. Commonly seen when football players arm tackle or when kayakers brace the paddle above their heads and allow their arms to get to far posterior. Radiographically seen as the humeral head lying inferior and medial to the glenoid.

A

Anterior shoulder dislocation

1396
Q

Humeral head often impacts on the inferior lip of the glenoid causing an indentation on the posterior superior portion of the humeral head. Its presence indicates a greater likelihood of recurrent dislocation and some surgeons use it as an indicator to intervene surgically to prevent recurrence.

A

Hill-Sachs deformity

1397
Q

A bony regularity or fragment of the inferior glenoid resulting from the impact of the humeral head on the inferior lip of the glenoid.

A

Bankart deformity

In Bankart deformity, the deformity is on the GLENOID whereas, in Hill-Sachs deformity, the deformity is on the HUMERAL HEAD.

1398
Q

Often mistaken for a dislocated shoulder. This disease entity displaces the humeral head inferoLATERALLY on the AP view.

A

Traumatic hemarthrosis

Anterior dislocation displaces the humeral head inferoMEDIALLY on AP view.

1399
Q

On Scap-Y / Transscapular view, the humeral head is displaced inferiorly in relation to the glenoid with absence of the crescent sign likely due to hemarthrosis. Not posteriorly or anteriorly displaced but INFERIORLY. Can suggest a subtle or occult humeral head fracture. Should be recognized to prevent attempts to reduce the shoulder.

A

Pseudodislocation of the shoulder

1400
Q

True or false:
In looking for secure fractures one should examine the arcuate lines of the sacrum bilaterally to see if they are symmetric or asymmetric. If these arcuate lines are interrupted it might be due to fracture.

A

True

1401
Q

Honda sign is a characteristic appearance of this fracture on radionuclide bone scan.

A

Bilateral Sacral stress fracture

Occurs in BILATERAL only, not UNILATERAL

1402
Q

Fractures that also have been termed “insufficiency fractures” indicating that the underlying bone is abnormal similar to a pathologic fracture.

A

Sacral stress fractures

1403
Q

Most serious stress fracture and is one of the rarest.

A

Femoral neck stress fracture / Stess fracture of the femoral neck

1404
Q

Misalignment of the medial border of the 2nd metatarsal to the medial border of the 2nd cuneiform (intermediate cuneiform) should suggest what

A

Lisfranc fracture-dislocation

1405
Q

Hallmarks of Osteoarthritis
“J.O.S.teoarthritis”

A

J-oint space narrowing
O-steophytosis
S-clerosis

1406
Q

Erosive osteoarthritis is a form of hand osteoarthritis associated with osteoporosis and erosions. Present radiographically with joint space narrowing, subchondral erosions, joint ankylosis. However, there is absence of marginal erosion, soft-tissue swelling, and osteopenia. (-) Rheumatoid factor, (-) ANA, Slightly elevated ESR/CRP. This is also known as…

A

Kellgren Arthritis

1407
Q

Exceptions to the classic triad of Degenerative joint disease / Osteoarthritis

A

TMJ, Acromioclavicular joint, Sacroiliac joint, Symphysis pubis

1408
Q

Radiographic hallmarks of rheumatoid arthritis:
“J.O.S.E. may Rheumatoid Arthritis”

A

J-oint space narrowing
O-steoPOROSIS
S-oft tissue swelling (STS)
E-rosions (marginal)

1409
Q

Associated with Swan neck deformity, which is hyperextension of the PIP with flexion of the DIP, and Boutonniere disease which is flexion of the PIP with extension if the DIP.

A

Rheumatoid arthritis

“‘WAN Button RA” pronounced as One Button Rebuildable atomizer (vape)
sWAN neck deformity
BUTTONniere disease

1410
Q

Migration of the femoral head in Osteoarthritis and Rheumatoid arthritis
“OAS.is AMun RA”

A

O-steo
A-rthritis
S-uperolaterally
i
s
A-xial
M-edial
u
N
R-heumatoid
A-rthritis

1411
Q

HLA-B27 Spondyloarthropathies
“HiLA para mag-A.P.I.R”

A

HiLA = HLA-B27
A-nkylosing spondylitis
P-soriatic arthritis
I-nflammatory / Enteropathic arthritis
R-eactive arthritis / R-eiter syndrome

1412
Q

Single/Unilateral Sacroiliac joint involvement

A

Reiter syndrome/Reactive arthritis
Psoriasis

“yung iisang SUSI nakay Reiter at Sora”
Iisang = One
S-ingle
U-nilateral
S-acro
I-liac joint I-nvolvement
Reiter disease
“Sora”iasis / Psoriatic arthritis

1413
Q

Bilateral sacroiliac joint involvement in HLA-B27 Spondyloarthropathies
“A.P.I.R. nga diyan, BILAT!

A

A-nklyosis spondylitis
P-soriatic arthritis
I-nflammatory bowel disease (Enteropathic arthritis)
R-eiter syndrome / Reactive arthritis
BILATeral

1414
Q

Metabolic disorder that results in hyperuricemia and leads to monosodium urate crystals being deposited in various sites in the body especially joints. Classic radiographic findings include well-defined erosions often with sclerotic borders or overhanging edges, soft tissue nodules that calcify in the presence of renal failure, and random distribution in the hands without marked osteoporosis. Typically effects metatarophalangeal joint of the great toe.

A

Gout

1415
Q

Most common location of chondrocalcinosis in CPPD

A
  • Knee
  • Symphysis pubis
  • Triangular fibrocartilage of wrist
1416
Q

Classic triad of Pseudogout / Calcium PyroPhosphate Deposition disease
“CPPD has CCPD”

A

C-artilage C-alcification
P-ain
D-estruction of joint

1417
Q

Classic radiographic findings of Gout
“I like my GOAT meat picked at RANDOM, SOFT, WELL-done, and OVERHANGING and NO burn Marks”

A

GOAT = Gout
RANDOM distribution
SOFT tissue nodules
WELL defined erosions with OVERHANGING edges
No marked osteoperosis

1418
Q

Three diseases that have a high degree of association with CPPD
“PGH”

A
  • Primary hyperparathyroidism
  • Gout
  • Hemochromatosis
1419
Q

Disease of excess iron deposition in tissues throughout the body leading to fibrosis and eventual organ failure. Radiographic changes include degenerative joint disease of the 2nd to 4th MCP joints, Squarring of the metacarpal heads appearing enlarged and block-like, and “drooping” osteophytes.

A

Hemochromatosis

1420
Q

Deposition of granulomatous tissue in the body, lungs, and bones. Predilection for the hands causing destructive lesions in the cortex with a lace like appearance which is characteristic. Skin nodules may also be appreciated in the hands.

A

Sarcoid

1421
Q

Hallmarks of a Neuropathic joint or Charcot joint

A
  • Joint destruction
  • Dislocation
  • Heterotropic new bone
1422
Q

Most commonly seen Neuropathic/Charcot joint today is

A

Diabetic foot

Typically affects 1st - 2nd tarsometatarsal joints in a fashion similar to Lisfranc fracture

1423
Q

Classic findings for juvenile rheumatoid arthritis and hemophilia

A

Overgrowth of the ends of the bones (epiphyseal enlargement) associated with gracile diaphysis (widening of the intercondylar notch of the knee)

1424
Q

Most likely cause for the overgrowth of the ends of the bones seen in JRA, hemophilia, and paralysis and is a common denominator shared by the three

A

Disuse

1425
Q

A relatively common disorder caused by a metaplasia resulting in deposition of cartilage in the joint. Most often calcify and are readily seen on radiograph. Most commonly seen in the knee, hip, and elbow. Classifications begin in the synovial and tend to shed into the joint where they can cause symptoms of free fragments “joint mice”

A

Synovial Osteochromatosis

1426
Q

Also known as Shoulder-Hand syndrome or Chronic regional pain syndrome. Typically occurs after a minor trauma to one extremity resulting in pain swelling and dysfunction. Radiographic findings include severe patchy (aggressive) osteoporosis and soft tissue swelling. Typically affects the distal part of an extremity such as a hand or foot. Intermediate joints such as knee and the hip are occasionally involved.

A

Sudeck atrophy

1427
Q

Uncommon chronic inflammatory process of the synovial that causes synovial proliferation. Swollen joint with lobular masses of synovial occurs and causes pain and joint destruction. Whenever this is considered, Synovial chondromatosis should be mentioned. Characteristic appearance on MRI shows low signal hemosiderin lining the synovial on T1 and T2.

A

Pigmented villonodular synovitis

1428
Q

Most reliable radiographic sign for knee effusion is

A

Distance between suprapatellar fat pad and the anterior femoral fat pad.

<5mm = normal
5-10mm = equivocal
>10mm = effusion

1429
Q

The only fat pad around the hip that gets displaced with hip effusion is the

A

Obturator Internus

1430
Q

True or false:
In the setting of trauma, elbow joint effusions indicate fractures. Other joint effusions are clinically obvious and do not require radiographic validation.

A

True.

1431
Q

Earliest sign of avascular necrosis or osteonecrosis in any joint

A

Joint effusion

1432
Q

Radiographic hallmark of Avascular necrosis/Osteonecrosis

A

Increased bone density at an otherwise normal joint

Increased bone density at a NARROWED joint indicates Degenerative joint disease, Not Osteonecrosis

1433
Q

True or false:
Presence of a subchondral lucency often develops which forms a thin line along the articular surface described as being an early indicator for Avascular necrosis.

A

False. It is a LATE sign for Avascular necrosis

1434
Q

A smaller and more focal form of AVN. Most likely caused by trauma. Occurs most often in the knee or medial epicondyle. Frequently leads to a smaller fragment of bone sloughed ofdlf and becoming a free fragment in the joint, “joint mouse/mice”

A

Osteochondritis dissecans

1435
Q

Avascular necrosis of the Navicular bone

A

Kohler disease

“KOH Ta Na” (Quota Na)
Kohler disease, Talus Navicular
“Legg = Femur”
Legg-Parthes, Femoral head
“LuBak”
LUnate, kieBOCK malacia
“naTATAMeme si Frei”
MeTaTarsals, Freiberg infarction
“Showman Fire Rings”
Scheuermann disease, APOYphyseal RINGS of vertebral bodies

1436
Q

Avascular necrosis of the metatarsal heads

A

Freiberg infarction

“KOH Ta Na” (Quota Na)
Kohler disease, Talus Navicular
“Legg = Femur”
Legg-Parthes, Femoral head
“LuBak”
LUnate, kieBOCK malacia
“naTATAMeme si Frei”
MeTaTarsals, Freiberg infarction
“Showman Fire Rings”
Scheuermann disease, APOYphyseal RINGS of vertebral bodies

1437
Q

Avascular necrosis of the femoral head

A

Legg-Parthes disease

“KOH Ta Na” (Quota Na)
Kohler disease, Talus Navicular
“Legg = Femur”
Legg-Parthes, Femoral head
“LuBak”
LUnate, kieBOCK malacia
“naTATAMeme si Frei”
MeTaTarsals, Freiberg infarction
“Showman Fire Rings”
Scheuermann disease, APOYphyseal RINGS of vertebral bodies

1438
Q

Avascular necrosis of the apophyseal rings of vertebral bodies

A

Scheuermann disease

“KOH Ta Na” (Quota Na)
Kohler disease, Talus Navicular
“Legg = Femur”
Legg-Parthes, Femoral head
“LuBak”
LUnate, kieBOCK malacia
“naTATAMeme si Frei”
MeTaTarsals, Freiberg infarction
“Showman Fire Rings”
Scheuermann disease, APOYphyseal RINGS of vertebral bodies

1439
Q

Main radiographic finding in osteoporosis

A

Thinning of the cortex

Most reliably demonstrated in the 2nd metacarpal at the mid diaphysis

1440
Q

Disuse osteoporosis is a type of osteoporosis that results from immobilization from any cause, most commonly follows

A

Treatment of a fracture

(Patient is just lying down on a bed after fracture treatment)

1441
Q

The only finding pathognomonic for osteomalacia (vs. osteoporosis). It is a fracture through the osteoid seams.

A

Looser fracture

1442
Q

Most common cause of osteomalacia in children

A

Rickets

Causes the epiphysis to become flared and irregular and the long bones to undergo pending from the bone softening.

1443
Q

Most common cause of primary hyperparathyroidism

A

Parathyroid adenoma (80%)

1444
Q

Most common cause of secondary hyperparathyroidism

A

Renal disease / Renal osteodystrophy with chronic hypocalcemia

1445
Q

Radiographic sign that is pathognomonic for hyperparathyroidism

A

Subperiosteal bone resorption

Most commonly seen on radial aspect of the middle phalanges of the hand, medial aspect of the proximal tibia, sacrum joints, and in the distal clavicle.

1446
Q

True or false:
Metabolic bone surveys are no longer recommended to assess bone lesions of Hyperparathyroidism

A

True

1447
Q

Clinically, you notice that a patient is obese and of short stature with round facies. Bilateral hand xray revealed brachydactyly in several of the metacarpals. Diagnosis?

A

Pseudohypoparathyroidism

1448
Q

Pituitary gland hyperfunction, due to secreting adenoma or hyperplasia of the anterior lobe of the pituitary gland, before the epiphysis close causes what?

A

Gigantism

1449
Q

Pituitary gland hyperfunction, due to secreting adenoma or hyperplasia of the anterior lobe of the pituitary gland, after the epiphysis close causes what?

A

Acromegaly

1450
Q

Patient presents with calvarial thickening, enlarged sinuses, and enlarged sella turcica. Prognathic jaw. Terminal tufts of the distal phalanges become hypertrophied and have a so called spade appearance. “Spade tufts”

A

Acromegaly

1451
Q

Congenital hypothyroidism / Thyroid gland HYPOfunction leads to decreased thyroid secretion, which results in delayed skeletal maturation in children

A

Cretinism

1452
Q

Bone infarcts, Step off deformities of the vertebral body endplates, and “fish” vertebrae (appearance like the vertebrae found in fish)

A

Sickle cell disease

1453
Q

A myeloproliferative neoplasm in which there is replacement of bone marrow with collagenous connective tissue and progressive fibrosis in patients older than 50 y/o. Leads to anemia, splenomegaly, and extramedullary hematopoiesis. Osteosclerosis is seen in patients older than 50

A

Primary Myelofibrosis

1454
Q

Pencil-in-cup deformity is classically associated with…

A

Psoriatic arthritis

However, it is not pathognomonic for it. It may also be seen in Rheumatoid arthritis and Reactive arthritis.

1455
Q

A congenital abnormality that demonstrates dense bones. Patients are typically short and have hypoplastic mandibles. Radiographic findings of acroosteolysis (a.k.a phalangeal osteolysis, refers to resorption of the distal phalanx. Terminal tuft most commonly affected) with sclerosis are pathognomonic. Distal phalanges have the appearance of chalk that has been put into a pencil sharpener.

A

Pyknodysostosis

Y = You, kno = Know, dys = This
“P-YouKnowThis-Ostosis” imagine a teacher pointing a sharp CHALK at you, with the Distal phalanx / Terminal tuft near the chalk as well.

1456
Q

This line in the pelvis MUST be thickened if Paget disease is present since the disease is almost commonly present in the pelvis

A

Iliopectineal line

1457
Q

Classification of this ligament is said to be characteristic of Fluorosis

A

Calcification of the sacrotuberous ligament

1458
Q

Dripping candle wax appearance of thickened cortical new bone that accumulates near the ends of long bones, usually on one side.

A

Melorheostosis / Leri disease

1459
Q

Classically described radiographic appearance is a cortically based sclerotic lesion in a long bone that has a small lucency within it called the nidus. A painful lesion that occurs almost exclusively in patients less than 30 years old. It is treated successfully with surgical excision or thermal ablation. When the nidus is surgically removed or thermally ablated, complete cessation of pain.

A

Osteoid osteoma

1460
Q

Osteoid osteoma will have an area of increased uptake corresponding to the area of reactive sclerosus but in addition, will demonstrate a secondary of increased uptake corresponding to the nidus. This has been termed…

A

“Double density” sign

1461
Q

Also known as Voorhoeve disease. Manifested by multiple 2-3 mm thick linear bands of sclerotic bone aligned parallel to the long axis of the bone. Usually affects multiple long bones and is asymptomatic.

A

Osteopathia striata

1462
Q

Hereditary, asymptomatic disorder that is usually an incidental finding of multiple small (3-10mm) sclerotic bony densities affecting primarily the pelvis and ends of long bones. Maybe confused for diffuse osteoblastic metastasis.

A

Osteopoikilosis

1463
Q

Rare, familial disease manifested by thickening of the skin of extremities and face, clubbing of fingers, and widespread periostitis. More common in black patients. Periosteal reaction is similar to hypertrophic pulmonary osteoarthropathy but is only occasionally painful. Characteristic lace-like pattern of bony destruction in the hands. Multiple calendars are typically affected in either or both hands.

A

Pachydermoperiostitis

1464
Q

Begins with a painful hip with no underlying disorder or other findings rather than osteoporosis which is limited to the painful hip. Self limited with full resolution. Occur more often in males. Percent with more edema than AVN and no well-demarcated margin is seen. Treated with pain management and protected weight bearing.

A

Transient osteoporosis of the hip / idiopathic transient osteoporosis of the hip (ITOH)

1465
Q

Also called Transient osteoporosis of the knee. Most commonly occurs in medial condyle but can occur in the proximal tibia. T2 with fat suppression shows marked high signal in the medial condyle in a middle-aged woman with sudden onset of pain. Pain resolved over a 6 month period. Protected weight-bearing is recommended. Edema has been reported. Can occur in several different locations over time or simultaneously and is then called regional migratory osteoporosis.

A

Painful bone marrow syndrome

1466
Q

Meniscal signal that does not disrupt an articular surface is representative of intrasubstance degeneration which is myxoid degeneration of the fibrocartilage. Most likely represents aging and normal wear and tear.

A

Meniscal degeneration

1467
Q

Grading scale for menisci:
Rounded or amorphous signal that does not disrupt an articular surface

A

Grade 1

1468
Q

Grading scale for menisci:
Rounded or linear signal that disrupts an articular surface

A

Grade 3, “Meniscal tear”

Note: Grade 1&2 are intrasubstance degeneration and NOT TEARS. If mentioned as a tear, may lead to unnecessary arthroscopy.

1469
Q

Grading scale for menisci:
Linear signal that does not disrupt an articular surface

A

Grade 2

1470
Q

Most common type of meniscal tear

A

Oblique tear (Extending to inferior surface of posterior horn of medial meniscus)

1471
Q

A displaced, vertical longitudinal meniscal tear that can result in the inner free edge of the meniscus displaced centrally and the humerus becoming displaced into the intercondylar notch. Commonly occurs with medial meniscus and are associated with ACL tears. On coronal view, meniscus may be shortened or truncated. Other findings include absent bow tie sign on sagittal view.

A

Bucket-handle tear

NOTE: Double PCL sign (bucket-handle tears of medial meniscus) and Double ACL sign (bucket-hand tears of lateral meniscus) on sagittal view.

1472
Q

Large meniscus that can have many different shapes such as lens shape, wedge or flat. More prone to tear than a normal meniscus. Can be symptomatic even without being torn. Easily identified on coronal view by noting extension of meniscal tissue into the tibial spines at the intercondylar notch.

A

Discoid meniscus

1473
Q

Most common appearance of ACL tear

A

Most often simply NOT VISUALIZED

1474
Q

Partial tears or sprains of the ACL present on MRI as

A

High signal within an otherwise intact ligament

1475
Q

This cruciate ligament is infrequently torn and even less frequently repaired by surgeons. When torn it appears as chicken and has diffuse intermediate signal throughout. Always thicker than 7 mm. Rarely a cause of instability.

A

Posterior cruciate ligament tear

1476
Q

This collateral ligament gets Injured usually from a valgus stress to the lateral part of the knee such as “clipping” injury in football.

A

Medial collateral ligament injury

1477
Q

Medial collateral ligament injury grading:
Represents a mild sprain and diagnosed on mri by presence of fluid or hemorrhage in the soft tissues medial to the MCL. Ligament is normal.

A

Grade 1

1478
Q

Medial collateral ligament injury grading:
Considered a partial tear and is seen as a high signal in and around the mcl on T1 and T2. Ligament is intact but deep and superficial fibers may show minimal disruption.

A

Grade 2, Partial tear

1479
Q

Medial collateral ligament injury grading:
Complete disruption of the MCL.

A

Grade 3, complete tear

1480
Q

Occurs when the medial meniscus is torn from its attachment to the joint capsule. Most commonly occurs at the site of the MCL and often occurs concomitantly with an MCL injury. Easily recognized on T2 coronal image by noting joint fluid extending between the medial meniscus and the capsule.

A

Meniscocapsular separation

1481
Q

Patellar cartilage commonly undergoes degeneration causing exquisite pain and tenderness. More easily identified on axial images. Begins with focal swelling and degeneration of the cartilage seen as high signal foci. Progression causes thinning and irregularity of the articular surface of the cartilage. Finally, the underlying bone is exposed. Final stage occurs more commonly from trauma than wear and tear.

A

Chondromalacia patella

1482
Q

An embryologic remnant from where the knee was divided into three compartments. It is a thin fibrous band that extends from the middle capsule toward the medial facet of the patella. On rare occasions, can thicken and cause clinical symptoms indistinguishable from torn meniscus termed “Plica syndrome”

A

Patellar plica

1483
Q

Most frequently encountered bony abnormalities seen with MRI

A

Bone Contusion

1484
Q

These represent microfractures from trauma and are also called bone bruises. On T1, subarticular areas often inhomogeneous low signal are seen. On T2, increased signal for several weeks depending on its severity. Can progress to osteochondritis dissecans if not treated with decreased weight-bearing.

A

Bone contusions

1485
Q

True or false:
An isolated bone contusion with no other internal derangement is a serious finding that requires protection.

A

True.

Bone contusion can progress to osteochondritis dissecans if not treated with decreased weight-bearing.

1486
Q

A bone contusion that occurs on the posterior part of the lateral tibial plateau have associated tears of what ligament in 90% of cases?

A

ACL tears, Acute ACL tears (90%) of cases

1487
Q

An avulsion fracture of the kneethat involves the lateral aspect of the tibial plateau and is very frequently (~75% of cases) associated with disruption of the anterior cruciate ligament (ACL). A small bony fragment pulled off the posterior lateral tibial joint line by an avulsion of the lateral joint capsule. It is almost always associated with an ACL tear.

A

Segond fracture

1488
Q

A bursal abnormality that can cause joint pain and clinically mimic a syndrome or a torn meniscus

A

Bursitis

1489
Q

True or false:
Pes Anserine Bursitis / bursa inflammation can mimic Plica syndrome and Torn medial meniscus.

A

True.

1490
Q

True or false:
Medial bursae inflammation / Medial bursitis can mimic Meniscal cysts

A

True.

1491
Q

Occurs from abduction of the humerus which allows the tendon to be impinged between the anterior acromion and the greater tuberosity. Can also be impinged by the undersurface of the AC joint if downward-pointing osteophytes or a thick and capsule is present.

A

Impingement of the supraspinatus tendon (Impingement syndrome)

1492
Q

True or false:
Joint effusion, when present, the intra-articular structures such as the labrum, biceps, and articular surface of the cuff are more easily evaluated.

A

True.

1493
Q

True or false:
Tendon degeneration (tendinopathy) is seen as a high signal in T1 that does not increase with T2. Can be seen asymptomatic shoulders of all ages. If the signal gets brighter on T2, must consider pathologic causes such as tendinitis or a partial tear.

A

True

1494
Q

True or false:
Partial tears have more clinical to clinical significance if they are greater than 25% of the cuff thickness.

A

True

1495
Q

A term of a particular type of articular sided partial tear. It occurs at the insertion of the fibers of the cuff onto the greater tuberosity. Most commonly occurs entirely at the insertion of the supraspinatus. It is the most commonly seen cuff tear on MRI.

A

Rim rent

1496
Q

This bony abnormality is a posterolateral humeral head depression fracture, resulting from the impaction with the anterior glenoid rim, and indicative of an anterior glenohumeral dislocation. Bony impaction on the posterior superior aspect of the humeral head can be seen in patients with anterior instability of the humeral head.

A

Hill-Sachs lesion

“Humeral Hill” Humeral head, Hill-Sachs lesion

1497
Q

Most common normal variant in the labrum that can mimic a torn or detached labrum

A

Sublabral recess (70% of shoulders)

Often seen on the oblique coronal images that can make a Superior Labrum Anterior to Posterior (SLAP) tear. Should only be thin, smooth and seen only in the anterior part of the superior labrum.

1498
Q

Difference between Tenosynovitis versus Tendinosis:

A

Tenosynovitis = Fluid seen in the tendon sheath surrounding an otherwise normal tendon

Tendinosis = Tendon is enlarged and/or has high signal within

1499
Q

True or False:
A subscapularis tear must be present if the biceps tendon is dislocated.

A

True

1500
Q

A fairly common finding is a ganglion in the spinoglenoid notch that impresses the infraspinatus portion of the nerve with resultant pain and atrophy of the infraspinatus muscle. Commonly seen in males were athletic particularly weightlifters. Always associated with a torn posterior labrum, and can clinically mimic rotator cuff tear.

A

Suprascapular nerve entrapment

1501
Q

Quadrilateral space syndrome most commonly occurs from

A

Fibrous bands or scar tissue in the quadrilateral space impinging on the axillary nerve

1502
Q

If supraspinatus is smaller than other muscles and/or fatty infiltration, this is the likely diagnosis

A

Suprascapular nerve entrapment, secondary to a ganglion in spinoglenoid notch

1503
Q

If the teres minor has fatty atrophy, this is most likely the diagnosis

A

Quadrilateral space syndrome

1504
Q

Neurogenic edema is found in muscle groups that correspond to a particular nerve. Not pathognomonic because a traumatic nerve injury could have a similar appearance. No history of trauma, sudden onset of severe pain, followed by profound weakness, and edema. Seems to have an association with prior vaccinations viral illness or general anesthesia.

A

Parsonage-Turner syndrome

Supraspinatus/infraspinatus = Suprascapular nerve
Teres minor/Deltoid=Axillary nerve

1505
Q

True or False:
Achilles tendon will not have tenosynovitis because it does not have a sheath associated with it.

A

True.

Tenosynovitis is fluid within a tendon sheath with underlying tendon normal. Since the Achilles tendon doesnt have a sheath, it cannot have tenosynovitis.

1506
Q

Rupture of the posterior tibial tendon results clinically in what kind of foot

A

Flat foot, due to loss of arch support

1507
Q

This ligament runs deep to the posterior tibial tendon and then goes underneath the neck of the talus which it supports in a sling like fashion. When the posterior tibial tendon tears, stress is then placed on this ligament to support to talus and the arch

A

Spring ligament

1508
Q

True or false:
Spring ligament as a high incidence of destruction when the posterior tibial tendon is torn.

A

True

1509
Q

This structure will be next to fail after the posterior tibial tendon and spring ligament tear from stress

A

Subtalar joint ligaments, in the sinus tarsi

1510
Q

Ballet dancers will often have tenosynovitis all this tendon, seen on MRI as fluid in the sheath surrounding the tendon. Rupture of this tendon is rare.

A

Flexor Hallucis Longus tendon (FHL)

1511
Q

Avulsion of the fifth metatarsal from a fool by the peroneus brevis tendon is known as

A

“Dancer’s fracture” or Jones fracture

1512
Q

Most commonly injured ligament in over 90% of ankle sprains

A

Lateral ligament

1513
Q

Patient presents with lateral ankle pain and tenderness and perception of hindfoot instability the ligaments are torn and the fat is replaced with granulation tissue or scar tissue. T2 High (granulation tissue) and T2 Low (scar), while T1 will be low in signal.

A

Sinus tarsi syndrome

1514
Q

Results from hypertrophy and scarring of the sinovium in the lateral gutter of the ankle. Patients present with lateral ankle pain and inability to dorsiflex normally. Often have a click on dorsiflexion. The anterior talofibular ligament is commonly torn or fibrosed.

A

Anterolateral impingement syndrome

1515
Q

Bony sequestrum
“E.L.F. O.n a QUEST”

A

E-osinophilic granuloma
L-ymphoma
F-ibrosarcoma
O-steomyelitis
QUEST = se-QUEST-rum

1516
Q

Bone lesions with No Periositits
”No Pera? FINES” (English of Oks lang)

A

F-ibrous dysplasia
I-nfection
N-on ossifying fibroma
E-nchondroma
S-olitary bone cyst

1517
Q

Painless bone lesions
“NO F.Eyn.S” (read as No Pains)

A

N-on O-ssifying fibroma
F-ibrous dysplasia
Eyn-chondroma
S-olitary bone cyst

1518
Q

Sclerotic bone lesions
“BIG FiDOO” if you remember, Fido dido was white like sclerotic

A

B-rown tumor
I-nfection
G-iant cell tumor
Fi-brous D-ysplasia
O-steoid O-steoma

1519
Q

Expansile lytic lesions of posterior elements of the spine:
“T.A.O lang ang nagpapalaki (expansile lytic) ng nakaraan (posterior elements)”

A

T-uberculosis
A-neurysmal bone cyst
O-steoblastoma

1520
Q

Also known as the superior sulcus tumor

A

Pancoast tumor

May be associated with SVC syndrome, Brachial plexus compression, and Horner syndrome

1521
Q

Barcode/stratosphere sign on chest ultrasound

A

Pneumothorax

1522
Q

Seashore sign on chest ultrasound

A

Normal chest lung on ultrasound

1523
Q

This modality provides the greatest anatomic detail in pelvic imaging

A

MRI of the female pelvis

1524
Q

A benign endometrial pathology that can cause mucous discharge or irregular vaginal bleeding. On ultrasound, represent as a focal nodular area of endometrial thickening with a feeding vessel by doppler. Hysterosonogram is definitive.

A

Endometrial polyp

1525
Q

A benign endometrial pathology that manifests as abnormal proliferation of the endometrial glands and stroma. Causes abnormal uterine bleeding. Etiology is unopposed estrogen stimulation (on Tamoxifen). On ultrasound, there is smooth endometrial thickening and or cystic changes.

A

Endometrial hyperplasia or metaplasia

1526
Q

True or false:
Larger endometrial polyps (>1.5 cm) in postmenopausal women have malignant potential.

A

True

1527
Q

Most common location of fibroid/leiomyoma

A

INTRAMURAL (within the myometrium)

1528
Q

Most common congenital uterine abnormality / malformation

A

Septate uterus, followed by bicornuate uterus

1529
Q

Women’s imaging:
On ultrasound, uterine enlargement with heterogenous and multicystic bunch of grapes appearance.

A

Complete hydatidiform mole, does not contain any fetal parts

Incomplete / partial mole contains fetal parts.

1530
Q

On second trimester scan, a thickened nuchal fold is suggestive of what syndrome

A

Down syndrome

1531
Q

On first trimester scan, a nuchal translucency of more than or equal to 3 mm is suggestive of

A

Aneuploidy, an abnormal number of chromosomes / chromosome abnormality

1532
Q

Amniotic fluid index of more than 25

A

Polyhydramnios

Most commonly associated with:
GI abnormalities, Severe CNS abnormalities, Swallowing problems, Twin-twin transfusion syndromes

1533
Q

Amniotic fluid index of less than 7

A

Oligohydramnios

Most commonly associated with:
Renal agenesis, Renal dysplasia, ARPKD, Congenital bladder outlet obstruction

1534
Q

Most common associated neural tube defect in Chiari II

A

Lumbar myelomeningocele

1535
Q

Chiari II malformation - flattened cerebellar hemispheres in the small posterior fossa

A

Banana sign

1536
Q

Chiari II malformation - flattening of the frontal bones

A

Lemon sign

1537
Q

Boomerang shape on antenatal ultrasound

A

Holoprosenceohaly

1538
Q

Most frequent occult cancer detected Carcinoma contained within the duct with an intact basement membrane in place. Lowest stage of breast cancer, Stage 0. Presents mammographically as classifications. On MRI, pattern of linear or segmental clumped enhancement.

A

Ductal carcinoma in situ (DCIS)

1539
Q

Most common subtype of breast cancer representing 70-80% of cases. Presents with palpable mass and on mammogram as irregular mass with spiculated margins and associated pleomorphic calcifications.

A

Invasive ductal carcinoma (IDC)

1540
Q

Breast malignancy that have tendency to spread through the breast tissue without forming a discrete mass. Very difficult to diagnose through mammography because it ranges from one-view asymmetry to architectural distortion to a spiculated mass.

A

Invasive lobular carcinoma (ILC)

1541
Q

It is an aggressive breast cancer where the tumor invades the dermal lymphatics. Patients have poor prognosis. Physical exam findings show erythema, edema, and firmness, peau d’ orange or orange peel appearance. On mammography, the affected breast is larger and denser, with trabecular and skin thickening. Primary differential is mastitis.

A

Inflammatory carcinoma

1542
Q

A form of DCIS that infiltrates the epidermis of the nipple. Presents with erythema, ulceration, and eczematoid changes of the nipple.

A

Paget disease of the nipple

1543
Q

True or false:
Cancers with HER2/neu overexpression may respond to monoclonal antibody trastuzamab (brand name Herceptin), or tyrosine kinase inhibitors such as Lapatinib.

A

True

1544
Q

True or false:
Triple-negative cancers are ER, PR, and HER2/neu negative, and the majority are biologically aggressive with poor prognosis.

A

True

1545
Q

Most common aneuploidy detected at birth

A

Trisomy 21, Down syndrome

1546
Q

Most accurate means for sonographic dating of pregnancy in the first trimester

A

Crown rump length (CRL)

1547
Q

Most common abnormalities that result in first trimester abortions

A

Trisomy 16 and 45,X

1548
Q

Most common clinically significant type of human chromosomal abnormality

A

Aneuploidy

1549
Q

Most common cause of maternal infection

A

Cytomegalovirus

1550
Q

Most prominent radiation-associated abnormalities are

A

CNS defects

1551
Q

Single most powerful marker in screening for down syndrome

A

Fetal nuchal translucency (1st trim)

1552
Q

Most common cardiac defect associated with infants with down syndrome

A

VSD

1553
Q

Leading cause of intestinal obstruction in the newborn

A

Duodenal atresia

1554
Q

One of the most important markers in most sensitive and specific marker for mid trimester detection of down syndrome

A

Nuchal fold

1555
Q

Most common pathologic condition of the umbilicus and is associated with what trisomy

A

Single umbilical artery, Trisomy 18

1556
Q

The single most common cause of mental retardation

A

Down syndrome, Trisomy 21

1557
Q

Cause of 95% stillbirth or spontaneous abortion

A

Trisomy 18

1558
Q

With the early rupture of the amnion, the fetal parts get entrapped in bands which reduces the flow on the affected limb causing amputation. On ultrasound, constriction rings around digits arms and legs swelling of extremities distal to constriction, facial clefts, cephalocele, club feet, club arms, micropthalmia, and other ocular anomalies.

A

Amniotic band syndrome

1559
Q

Most characteristic prenatal feature of turner syndrome

A

Cystic hygroma

1560
Q

True or false:
Twin-twin transfusion syndrome only occurs in monochorionic, diamniotic pregnancy.

A

True

1561
Q

First definitive finding to SUGGEST early intrauterine pregnancy

A

Gestational sac

1562
Q

True or false:
Gestational sac should be detected by transvaginal sonography or transabdominal sonography when mean sac diameter (MSD) is at least 4 mm.

A

False. 5mm

1563
Q

Most common congenital CNS malformations

A

Neural tube defects

1564
Q

Most common syndrome associated with agenesis of the corpus callosum

A

Aicardi syndrome

1565
Q

Most common craniosynostosis

A

Scaphocephaly

1566
Q

Most common spinal abnormalities seen in skeletal dysplasia

A

Platyspondyly

1567
Q

Most common non-lethal skeletal dysplasia

A

Achondroplasia

1568
Q

Most common congenital diaphragmatic hernia is

A

Bochdalek hernia

1569
Q

Most common cause of congenital hydrothorax

A

Chylothorax

1570
Q

It is the leading cause of meconium ileus

A

Cystic fibrosis

1571
Q

Most common location of duplication cyst in the small bowel

A

Terminal ileum, at its mesenteric side

1572
Q

Most common origin of intestinal obstruction in the neonate

A

Hirschsprung disease

1573
Q

Most common congenital anal anomaly

A

Anal atresia

1574
Q

Most common type of anal atresia

A

Low

1575
Q

Most common benign tumor of the liver in fetus and units

A

Hemangioma

1576
Q

Most common hepatic malignancy in young children

A

Hepatoblastoma

1577
Q

Most common cause of obstructive jaundice in the newborn

A

Biliary atresia

1578
Q

Most common location of ectopic kidneys

A

Pelvis

1579
Q

Most common cause of urinary tract dilatation in the newborn

A

UPJ obstruction

1580
Q

Most common cause of non inherited renal cysts

A

Parenchymal dysplasia

1581
Q

Most common cause of inherited renal cystic disease

A

ADPKD

1582
Q

Most common origin of congenital abdominal masses

A

Kidneys

1583
Q

Most common renal tumor in the fetus

A

Mesoblastic nephroma

1584
Q

Most common site of placental abruption

A

Placental edge, Marginal

1585
Q

Most common cause of bleeding in the third trimester

A

Placenta previa

1586
Q

Placenta that is adherent to villa

A

Placenta accreta

1587
Q

Placenta that invades myometrium

A

Placenta increta

1588
Q

Placenta that perforate serosa or surrounding structures

A

Placenta percreta

1589
Q

Most common non trophoblastic placental tumor

A

Chorioangioma

1590
Q

Most common benign neoplasm of the placenta

A

Chorioangioma

1591
Q

Most common tumor of the umbilical cord

A

Hemangioma

1592
Q

Most common ovarian germ cell tumor

A

Ovarian teratoma

1593
Q

Most common type of ovarian teratoma

A

Mature cystic teratoma or dermoid cyst

1594
Q

Most common location of an abdominal ectopic pregnancy

A

Broad ligament

1595
Q

Viral etiology that causes cervical cancer

A

HPV 16, 18

1596
Q

Most common sex cord tumor of the ovaries

A

Fibroma

1597
Q

Most common primary ovarian carcinoma

A

Epithelial type

1598
Q

Most common site of metastasis to female genital tract

A

Ovaries

1599
Q

These endometrial abnormalities are hyperplastic growths consisting of dense fibrous tissue or smooth muscle with disorganized endometrial glands

A

Endometrial polyps

1600
Q

An extreme form of mullerian duct anomaly with complete agenesis of the proximal vagina and anomalous cervix and uterus and patients usually present in early puberty with primary amenorrhea

A

Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH)

1601
Q

Complete or partial agenesis of a unilateral mullerian duct leads to development of what anomaly of the uterus?

A

Unicornuate uterus

1602
Q

Most common type of mullerian anomaly

A

Septate uterus

1603
Q

A normal variant of uterine configuration in which the thickened fundal portion of the myometrium slightly indents the endometrial canal creating a heart shape endometrial cavity

A

Arcuate uterus

1604
Q

This is a disease characterized by migration of endometrial glands and stroma from the stratum basale into the myometrium often occurring in association with the reactive hyperplasia of the surrounding myometrial smooth muscle.

A

Adenomyosis

1605
Q

Retention cyst that develop secondary to obstruction of the cervical glands or crypts are called

A

Nabothian cysts

1606
Q

These lesions appear on ultrasound images as well circumscribed masses of variable echogenicity seen in the cervix and are typically relatively avascular

A

Cervical leiomyoma

1607
Q

Adnexal pathology that occurs when there is partial or complete rotation of the adnexal structures around there was fear pedicle with associated obstruction of venous outflow and arterial inflow

A

Adnexal torsion

1608
Q

Most consistently reported grayscale ultrasound finding of adnexal torsion

A

Unilateral enlarged ovary (>4cm) with or without an associated mass

1609
Q

This sonographic sign is described as a perifollicular hyperechoic rim that is 1-2 mm in thickness, seen surrounding the small peripheral antral follicles of the torsed ovary

A

Follicular ring sign

1610
Q

Most henorrhagic cysts typically resolve within how many weeks?

A

8 weeks

1611
Q

A sign of pelvic inflammatory disease wherein there are thickened and inflamed endosalpingeal folds that may suggest small mural nodules, that help differentiate pyosalpinx from an inflamed appendix.

A

Cogwheel sign

1612
Q

Most frequent site of extrapelvic disease

A

Anterior abdominal wall

1613
Q

This is a sonographic confirmatory diagnostic sign of leiomyoma wherein there is demonstration of a vascular supply into a mass derived from the uterus

A

Bridging vascular sign

1614
Q

Most common type of benign degeneration of leiomyoma

A

Hyaline degeneration

1615
Q

An acute form of benign leiomyoma degeneration is

A

Red degeneration

1616
Q

This sonographic finding is highly specific of a hemorrhagic ovarian cyst

A

Retracting clot

1617
Q

Most significant potential complication of a hemorrhagic ovarian cyst

A

Rupture with hemoperitoneum

1618
Q

Characteristic sonographic appearance of a mature cystic teratoma wherein there are areas of marked acoustic shadowing of the echogenic cyst contents of sebum and hair

A

Tip of the iceberg sign

1619
Q

This refers to the hyperechoic component of a mature cystic teratoma that typically corresponds to mixed hair and sebaceous material or occasionally to classification, sometimes related to a bone or tooth

A

Rokitansky nodule, Dermoid plug

1620
Q

This type of epithelial ovarian carcinoma is highly aggressive that present with advanced stage at diagnosis and likely originated from precursors arising in the fibriated segments of the fallopian tube epithelium.

A

Type II

1621
Q

This type of epithelial ovarian carcinoma is composed of low-grade neoplasms that present at an early age with an indolent course and are believed to arise from precursor lesions in the ovary, such as cortical inclusion cysts lined by tubal epithelia, serous cystadenomas, borderline neoplasms, or endometriosis

A

Type I

1622
Q

Most important sonographic feature for predicting ovarian malignancy

A

Presence of a solid component

1623
Q

Primary consideration once a solid ovarian mass is seen

A

Sex cord stromal tumor

1624
Q

Granulosa cell tumors most commonly secrete what hormone?

A

Estrogen

1625
Q

Sertoli-Leydig cell tumor most commonly secrete hormone?

A

Androgens, Testosterone

1626
Q

These ovarian tumors are uncommon surface epithelial tumors that often differ from others in that they are mostly solid appearing with internal classifications and are generally benign

A

Brenner tumors

1627
Q

Primary consideration if one encounters a lobulated solid ovarian mass particularly in a 20 to 30 year old woman

A

Dysgerminoma

1628
Q

A sonographic sign of tubal dilatation wherein the dilated tube folds back on itself and there is juxtaposition of the two inner folds of the fallopian tube

A

Incomplete septation sign

1629
Q

Hallmark of pelvic inflammatory disease

A

Sonographic involvement of the fallopian tube or ovary

1630
Q

Tuberculosis reaches and infects the fallopian tubes most commonly via what route?

A

Hematogenous route

1631
Q

In the non pregnant patient, hematosalpinx is most commonly due to what disease

A

Endometriosis

1632
Q

Primary fallopian tube carcinoma has a classical clinical presentation of LATZKO’S TRIAD composed of:

A
  • Pelvic mass
  • Vaginal discharge (bloody)
  • Colicky pain (relieved by the discharge)
1633
Q

Most common predisposing factor for ectopic pregnancy

A

Tubal scarring secondary to sexually transmitted infections (STI)

1634
Q

What disease is characterized by nodular thickening of the isthmic portion of the fallopian tube accompanied by multiple diverticula

A

Salpingitis isthmica nodosa

1635
Q

Term referring to a pregnancy that is detected biochemically but not yet visible sonographically or laparoscopically

A

Pregnancy of Unknown Location

1636
Q

Most reliable sonographic finding for ectopic pregnancy with a 100% positive predictive value

A

Extrauterine embryo with or without a heartbeat

1637
Q

Transvaginal ultrasound reveals an hourglass shaped uterus composed of a uterine corpus and disproportionately enlarged cervix with a “waist” at the level of the internal os. There is trophoblastic flows seen. Diagnosis is likely what?

A

Cervical pregnancy

1638
Q

Transvaginal ultrasound shows two endometrial cavity with a midline partition extending into the internal cervical os. A single cervix is present. The outer fundal contour of the uterus appears broad. This likely represents what anomaly of the reproductive tract?

A

Septate uterus

1639
Q

The most common anomaly of the female reproductive tract

A

Imperforate hymen

1640
Q

The usual cause of prepubertal bleeding

A

Vulvovaginitis

1641
Q

Most common vaginal foreign body in pediatric or adolescent patients

A

Fibrous material from clothing

1642
Q

Most frequent ovarian malignancy in childhood

A

Dysgerminoma

1643
Q

AAST Liver injury grading:
- Laceration <1 cm
- Subcapsular hematoma <10% surface area

A

Grade 1

1644
Q

AAST Liver injury grading:
- Laceration 1-3 cm, <10 cm in length
- Subcapsular hematoma 10-50% surface area
- Intraparenchymal hematoma <10 cm

A

Grade 2

1645
Q

AAST Liver injury grading:
- Laceration >3 cm
- Subcapsular hematoma >50% surface area
- Intraparenchymal hematoma >10 cm
- Vascular injury with active bleeding contained within liver parenchyma

A

Grade 3

1646
Q

AAST Liver injury grading:
- Laceration with parenchymal disruption 25-75% of liver or involves 1-3 Couinaud segments
- Vascular injury with active bleeding breaching liver parenchyma into peritoneum

A

Grade 4

1647
Q

AAST Liver injury grading:
- Laceration with parenchymal disruption >75% of hepatic lobe
- Vascular injury involving juxtahepatic venous injuries (IVC, Central major hepatic veins)

A

Grade 5

1648
Q

AAST Splenic injury scale:
- Subcapsular hematoma <10% surface area
- Parenchymal laceration < 1 cm
- Capsular tear

A

Grade 1

1649
Q

AAST Splenic injury scale:
- Subcapsular hematoma 10-50% surface area
- Parenchymal laceration 1-3 cm
- intraparenchymal hematoma <5 cm

A

Grade 2

1650
Q

AAST Splenic injury scale:
- Subcapsular hematoma >50% surface area
- Parenchymal laceration >3 cm
- intraparenchymal hematoma >5 cm

A

Grade 3

1651
Q

AAST Splenic injury scale:
- Splenic vascular injury or active bleeding CONFINED within splenic capsule
- Laceration involving segmental or hilar vessels producing >25% devascularization

A

Grade 4

1652
Q

AAST Splenic injury scale:
- SHATTERED SPLEEN
- Splenic vascular injury with active bleeding extending beyond the splenic capsule into the peritoneum

A

Grade 5

1653
Q

AAST Renal injury scale:
- Subcapsular hematoma or contusion
- No laceration

A

Grade 1

1654
Q

AAST Renal injury scale:
- Hematoma confined within perirenal fascia
- Laceration <1 cm

A

Grade 2

1655
Q

AAST Renal injury scale:
- Vascular injury or active bleeding CONFINED within perirenal fascia
- Laceration >1 cm not involving collecting system

A

Grade 3

1656
Q

AAST Renal injury scale:
- Vascular injury or active bleeding BEYOND perirenal fascia
- Laceration involving collecting system with urinary extravasation
- Vascular injury to SEGMENTAL renal artery or vein

A

Grade 4

1657
Q

AAST Renal injury scale:
- SHATTERED KIDNEY
- Avulsion of renal hilum or laceration of main renal artery or vein
- Devascularized kidney with active bleeding

A

Grade 5

1658
Q

Stanford classification of Aortic dissection:
Involves any part of the aorta proximal to the origin of the left subclavian artery

A

Stanford A
“Stanford A A-ffects A-scending A-orta”

1659
Q

Stanford classification of Aortic dissection:
Arises distal to the left subclavian artery origin

A

Stanford B
B for Baba = Descending aorta

1660
Q

DeBakey classification of Aortic Dissection:
Involves ascending and descending aorta (Stanford A)

A

DeBakey Type I

1661
Q

DeBakey classification of Aortic Dissection:
Involves ascending aorta ONLY (Stanford A)

A

DeBakey type II

1662
Q

DeBakey classification of Aortic Dissection:
Involves descending aorta ONLY, commencing after origin of left subclavian artery (Stanford B)

A

DeBakey type III

1663
Q

Most common location of thoracic aortic aneurysm

A

Ascending aorta, Aortic root (60%)

1664
Q

Most frequently injured viscous secondary to penetrating injury (firearms & stabbing)

A

Liver

1665
Q

Most common cause of subcapsular liver hematoma

A

Iatrogenic hepatic injury secondary to liver biopsy

1666
Q

A self-limiting, viral type of illness which is referred to as Valley fever when associated with erythema nodosum and arthralgias. Chest radiographs may be normal or show focal or multifocal segmental airspace opacities that resolve over several months. Hilar and mediastinal adenopathy and pleural effusions may be seen.

A

Acute coccidioidomycosis

“Cox Valley”
C. immitis
Coccidioidomycosis
Valley fever

1667
Q

Also known as fungus ball, consisting of hyphae, mucous, and cellular debris that colonizes a pre-existing bulla or a parenchymal cavity created by some other pathogen or destructive process. It is usually asymptomatic but may cause hemoptysis which may be massive. Presents as a solid round mass within an upper lobe cavity with an “Air crescent” sign separating from the cavity wall.

A

Aspergilloma / Mycetoma

1668
Q

Pulmonary disease caused by the Lung fluke. Acquired by eating raw crabs for snails. Patients may be asymptomatic or present with cough, hemoptysis, dyspnea, and fever. Radiographic findings include: multiple cysts with variable wall thickness, cystic opacities may become congruent with focal atelectasis and sub-segments of consolidation, dense linear densities representing burrows of the organism.

A

Paragonimiasis

By Paragonimus westermani

1669
Q

Refers to the extension of an empyema out of the pleural space and into the neighboring chest wall and surrounding soft tissues

A

Empyema necessitans / Empyema necessitatis

1670
Q

A rare complication of pulmonary infection when a portion of the lung is sloughed off. Imaging findings include an ordered aura mass within a cavity with a crescent of air surrounding the sloughed portion of the lung.

A

Pulmonary gangrene

1671
Q

Uncommon post-infectious form of constrictive bronchiolitis that typically results from severe viral or mycoplasma infection in infancy or childhood. Radiologic findings include: hyperlucent lung with normal or small-volume, attenuated vasculature, expiratory air trapping, and occasional proximal bronchiectasis.

A

Swyer-James syndrome

1672
Q

Honeycomb cysts are frequently seen in:

“Honey, don’t C.U.Ss in front of the kids”

A

C-hronic hypersensitivity pneumonitis
U-sual interstitial pneumonitis
S-arcoidosis

1673
Q

True or false:
Cysts of LCH and LAM have shared walls.

A

False. Honeycomb cysts have shared walls whereas the cysts in LCH and LAM do not.

1674
Q

True or false:
Honeycomb cysts tend to occur in the subpleural regions of lower lobes. Cysts of LCH and LAM are usually evenly distributed from central to peripheral in the upper lobes with or without lower lobe involvement.

A

True.

1675
Q

True or false:
Honeycomb cysts uniformly destroys lung and produces distortion of the lung interfaces and traction bronchiectasis.

A

True.

1676
Q

Disease of young and middle-aged women typically involve inflammation of multiple organs mediated by autoantibodies and circulating immune complexes. Radiographic findings include pleural effusions and pleural fibrosis, which may result in diffuse pleural thickening (present in long-standing disease)

A

Systemic lupus erythematosus (SLE)

1677
Q

Pulmonary disease associated with SLE presenting with rapid onset of fever, dyspnea, and hypoxemia and may require mechanical ventilation. Indistinguishable from ARDS with diffuse alveolar damage producing an exudative intra-alveolar edema with hyaline membrane formation. Present radiographically as rapidly coalescent bilateral airspace opacities and on CT scan as ground-glass opacities. Diagnosis by excluding pneumonia and pulmonary edema and improvement following immunosuppressive therapy.

A

Acute lupus pneumonitis

1678
Q

Produces inflammation and fibrosis of the skin, esophagus, musculoskeletal, lungs, kidneys in young and middle-aged women. Lungs are involved in nearly 90%. Pulmonary testing is more sensitive than conventional radiographs and shows typical diminished lung volumes, preserved flow rates, and low diffusing capacity. Pulmonary arterial hypertension with enlarged pulmonary arteries and right ventricular dilatation is seen in 50% of patients.

A

Scleroderma (Progressive systemic sclerosis)

Thickening and obliteration of small muscular pulmonary arteries and arterioles are responsible for development of pulmonary arterial hypertension in Scleroderma.

1679
Q

Autoimmune inflammation and destruction of skeletal muscle resulting in proximal muscle pain and weakness and skin rash. Thoracic manifestations include respiratory and pharyngeal muscle weakness. Fine reticular interstitial pattern in acute disease leads to a chronic course, reticular, and reticulonodular process predominantly basilar in distribution. Other radiographic findings: small lung volumes, diaphragmatic elevation, basilar linear atelectasis. Pharyngeal and upper esophageal muscle weakness predisposed to aspiration pneumonia.

A

Dermatomyositis and Polymyositis

1680
Q

Subacute illness with several months history of nonproductive cough and dyspnea. PFTs show restrictive pattern with diminished lung volumes and normal to increased flow rates. Histopath: Mononuclear cell exudate in bronchioles and surrounding alveoli organizes to form intro bronchial and intra-alveolar granulation tissue. Radiologic findings: patchy ground glass opacities surrounded by crescentic regions of more dense consolidation turned “reversed halo” sign.

A

Cryptogenic Organizing Pneumonia (COP)

1681
Q

This sign is also known as the ATOLL SIGN. On chest CT, seen as central ground-glass opacitysurrounded by denser consolidation of crescentic shape (forming more than three-fourths of a circle) or complete ring.

A

Reverse halo sign

As seen in Organizing pneumonia, Cryptogenic Organizing Pneumonia

1682
Q

Interstitial pneumonia that is characterized by accumulation of macrophages within the alveolar spaces

A

Desquamative interstitial pneumonia

1683
Q

Eggshell calcifications in Thorax and Mediastinum:
“Silly Sarco Likes Her Smart ABC while Mike likes EGGS”

A

“Silly Sarco Likes Her Smart ABC and Mike likes EGGS”

S:silicosis(5%)
S:sarcoidosis: (5%)
L:lymphoma (postradiation Hodgkin disease, usually 1-9 years following treatment)
H:histoplasmosis (rare)
S:scleroderma(rare)
A:amyloidosis(rare)
B:blastomycosis(rare)
C:coal workers’ pneumoconiosis(1%)
M: mycobacterium tuberculosis

1684
Q

This inhalational disease is seen pathologically as a large number of bodies with a transparent core surrounded by a coat of iron and protein deposited in lung tissue

A

Asbestos bodies in Asbestosis

1685
Q

This inhalational disease has pathologic findings of nodules with dense concentric lamellae of collagen in lung tissue.

A

Silicotic nodules in Silicosis

1686
Q

This inhalational disease is caused by inhaling large amounts of carbon containing inorganic material. Results from deposit of carbonaceous material within the lung. Appear as round or stellate nodules ranging in size from 1 to 5 mm. Pathologically seen as pigment laden macrophages with minimal or absent collagen formation.

A

Coal dust macule in Coal Worker’s Pneumoconiosis

1687
Q

This is also known as Extrinsic Allergic Alveolitis. This is an immunologic pulmonary disorder associated with inhalation of one of the antigenic organic dusts. Mediated by Type 3 hypersensitivity reaction. Radiographic findings include: fine nodular or ground glass opacities in the lower lobes or progressive airspace opacification which may resolve within hours to days. Chronic changes include: diffuse course reticular or reticulonodular opacities in the mid lung and upper lung zones, honeycombing with loss of lung volume.

A

Hypersensitivity pneumonitis

1688
Q

Schaumann bodies, which are laminated calcium-containing concretions, are characteristic of this granulomatous disease.

A

Sarcoidosis

1689
Q

Granulomatous disease with early histopathologic changes showing palisading epithelioid histiocytes with intermixed multinucleated giant cells

A

Schaumann bodies in Sarcoidosis

1690
Q

Bowler hat sign

A

GI polyps or diverticulum

The orientation of the bowler hat helps differentiate between the two conditions. When the top of the bowler hat is directed towards the center of the long axis of the colonic lumen it is a polyp.When the bowler hat is directed away from the colonic lumen it is a diverticulum.

1691
Q

Pathologically demonstrates multiple small nodules found predominantly in the axial interstitial tissues of the upper and mid lung zones around small bronchioles around small bronchioles. These are composed predominantly of cells with eosinophilic cytoplasm.

A

Langerhans cell histiocytosis

1692
Q

Systemic autoimmune disorder characterized pathologically by a necrotizing granulomatous vasculitis involving the upper and lower respiratory tracts and kidneys. Characteristic lesions in the lungs are discrete nodules or masses of granulomatous inflammation with central necrosis and cavitation. High serologic titers of antineutrophil cytoplasmic antibody are specific for the diagnosis.

A

Wegener granulomatosis

1693
Q

Most commonly results from damage to type 2 pneumocytes secondary to acute insult to the lungs. Initially manifests as pulmonary edema in a geographic or non-dependent distribution without pleural effusion interlobular thickening.

A

Diffuse alveolar damage (DAD)

1694
Q

Drugs that induce Diffuse Alveolar Damage:
“DAD is OP (Overpowered), drinks CHEvas GOLD, eats MIT (meat)”

A

D-iffuse A-lveolar D-amage
OP-iates
CHE-motherapeutic agents
GOLD
MIT-omycin

1695
Q

Characterized by formation of bone within lung parenchyma.

A

Diffuse pulmonary ossification

1696
Q

Diffuse tracheal and central bronchial dilatation resulting from an acquired or congenital defect of tracheal cartilage. Acquired more common. Imaging hallmark: excessive airway collapse on expiration. On CT: “FROWN-LIKE” configuration / Frown sign on Axial

A

Tracheobronchomalacia (TBM)

Frown sign = caused by anterior bowing of the posterior tracheal wall during expiration on Axial view

1697
Q

Production of abnormally thick tenacious mucus which plugs the small airways causing bronchial obstruction in dyspnea. Radiographs show hyperinflation with predominantly upper lobe bronchiectasis with mucous plugging. Diagnosis: Positive family history and sweat test showing an abnormally high concentration of chloride.

A

Cystic fibrosis

1698
Q

Abnormal and ineffective epithelial cilia motion resulting in rhinitis, sinusitis, bronchiectasis, dysmotile spermatozoa and sterility, situs inversus and dextrocardia. Associated with Kartagener syndrome (Sinusitis, Situs inversus, Bronchiectasis). Diagnosis: Clinical & Radiographic findings and nasal biopsy samples of CILIA anatomy and motion samples.

A

Dysmotile cilia syndrome

1699
Q

Type of emphysema that is characterized by airspace distension in the central portion of the lobule and sparing of the distal portions

A

Centrilobular emphysema

1700
Q

Type of emphysema that is seen as selective distention of the peripheral airspaces adjacent to interlobular septa with sparing of the centrilobular region

A

Paraseptal emphysema

1701
Q

Cigarette smoking is associated predominantly with what type of emphysema

A

Centrilobular emphysema

1702
Q

A sign of pneumothorax in the SUPINE patient:
When both diaphragmatic dome and anterior portions of the diaphragm are visualized (being outlined by lung and pleural air). Air may outline the anterior portions of the hemidiaphragm and cause visualization of the anterior costophrenic sulcus.

A

Double diaphragm sign

1703
Q

Most common primary malignancies to produce secondary spontaneous pneumothorax

A
  • Osteogenic sarcoma
  • Lymphoma
  • Germ cell malignancies
1704
Q

A rare type of pneumothorax that occurs with menstruation. Effects women in their fourth decade and is most likely caused by cyclic necrosis of pleural endometrial implants which creates an air leak between the lung and pleura. Manage by preventing menstruation with oral contraceptives.

A

Catamenial pneumothorax

1705
Q

HOLLY LEAF sign refers to the appearance of this benign pleural manifestation of ASBESTOSIS on chest radiographs. Their irregular thickened nodular edges are likened to the appearance of a holly leaf.

A

Pleural plaques

1706
Q

Prevention of contralateral mediastinal shift despite extensive pleural tumor volume and effusion is a finding that helps distinguish this asbestos-related pleural disease from metastatic disease.

A

Mesothelioma

1707
Q

Lipoma that may be intra or extrathoracic and may project partially within and outside the thorax

A

Dumbbell lipoma / Dumb-bell lipoma / Dumb bell lipoma

1708
Q

A relatively common congenital anomaly which arises from the 7th cervical vertebral body. It is usually is asymptomatic and a minority of cases present with secondary weakness and swelling of the upper extremity. Surgical resection can relieve the symptoms.

A

Cervical rib

1709
Q

Congenital anomalies of the bony thorax:
These may be associated with thin, wavy, “RIBBON” RIBS

A

Neurofibromatosis and Osteogenesis imperfecta

1710
Q

What vessels are particularly involved in rib notching from Coarctation of the aorta?

A

Intercostal arteries

The tortuosity and dilatation of these vessels causes erosion of the INFERIOR MARGIN of the adjacent ribs. Also, notching predominantly affects the POSTERIOR aspect of ribs bilaterally. So, a possible answer in PBR2 maybe “Posteroinferior” margin or either of the two separately.

1711
Q

A type of vertebral anomaly and results from a lack of formation of one half of a vertebral body. It is a common cause of congenital scoliosis.

A

Hemivertebra/e

1712
Q

Hemivertebra/e are associated with:

A
  • Cleidocranial dysostosis (partial or complete aplasia of the clavicle)
  • Gastroschisis
  • VACTERL association
  • Mucopolysaccharidosis
1713
Q

A type of vertebral anomalythat results from the failure of fusion of the lateral halves of the vertebral body because of persistent notochordal tissue between them.

A

Butterfly vertebra/e

1714
Q

Butterfly vertebra/e are associated with:

A
  • Anterior spina bifida
  • Anterior meningocele
  • VACTERL
1715
Q

STERNUM related abnormality:
- Heart displaced to LEFT
- Depressed soft tissues of anterior chest wall
- VERTICALLY oriented anterior ribs results in loss of right heart border

A

Pectus excavatum

1716
Q

Rounded, oval, or branching central lung opacity representing the obstructed, mucus-filled, dilated bronchus (mucocele/bronchocele) with hyperlucency in that portion of the lung supplied by the stenotic bronchus. Diagnosis: Central mucocele/bronchocele with peripheral hyperlucency in a young, asymptomatic patient.

A

Bronchial atresia

1717
Q

Echocardiography:
Increased E-F slope is associated with?
“E.T.A (Estimated Time of Arrival)”

A

-Ebstein anomaly
-Tricuspid regurgitation
-ASD

1718
Q

Most common morphologic variant of Hypertrophic cardiomyopathy present in 60-70% of cases?

A

Asymmetric hypertrophic cardiomyopathy / Asymmetric septal hypertrophy (ASH)

1719
Q

Subtype of Subvalvular / Subaortic stenosis:
Thin membrane less than 2 cm below the valve

A

Type 1

1720
Q

Subtype of Subvalvular / Subaortic stenosis:
Thick, collar type constriction

A

Type 2

1721
Q

Subtype of Subvalvular / Subaortic stenosis:
Irregular, fibromuscular type of narrowing

A

Type 3

1722
Q

Subtype of Subvalvular / Subaortic stenosis:
FUNNEL-like constriction

A

Type 4

1723
Q

True or false:
Valvular pulmonic stenosis is caused by PARTIAL FUSION in 95% of cases

A

True

1724
Q

Pulmonary valve cusps are immobile, thick, and redundant. No click noted and no post-stenotic dilatation.

A

Dysplastic pulmonary stenosis

1725
Q

Most common fungal agent in endocarditis

A

Candida

Followed by Aspergillus

1726
Q

These can be detected in 50-90% of patients with known bacterial endocarditis. Cause excessive vibration of the valves during systole and the leaflets may appear slightly thickened or fuzzy. Cause valvular incompetence or acute aguilar destruction. Remain even after successful antibiotic therapy.

A

Valvular vegetations, from Bacterial endocarditis

1727
Q

What is the pericardial disease?
- Calcified or fibrous thickening or the pericardium
- Chronically Compromise diastolic filling
- post-periCardiotomy is most common cause.

A

Constrictive pericardial disease

1728
Q

Widely swinging cardiac silhouette on DECUBITUS VIEW

A

Congenital abscence of the pericardium

1729
Q

Loud, continuous, MACHINE-like murmur

A

Patent ductus arteriosus (PDA)

1730
Q

Results from a deficiency in the supporting structure of the aortic valve cusps. Results in aneurysmal bulging of the aortic sinuses and in some cases, rupture. Most often affected is the RIGHT ANTERIOR aortic sinus.

A

Ruptured aneurysm of sinus of valsalva

1731
Q

Type of Pulmonary Atresia:
- RV is severely hypoplastic
- tricuspid valve is atretic
- no significant tricuspid regurgitation
- no RAE
- Intact intraventricular septum

A

Type 1

1732
Q

Type of Pulmonary Atresia:
- RV more developed
- Tricuspid valve more patent
- Gross tricuspid insufficiency
- Marked enlargement of RA
- Intact intraventricular septum

A

Type 2

1733
Q

Small hypoplastic RV and Tricuspid valve are present. RV pressures are exceedingly high, Shunting from right to left occurs at Atrial level. On Chest xray, decreased pulmonary vascularity and a shallow or concave pulmonary artery.

A

Pulmonary atresia

1734
Q

Cardiac anomalies that result in DECREASED PULMONARY VASCULARITY:
“Tetra H.U.E”

A
  • TETRAlogy of fallot
  • Hypoplastic right heart syndrome (Pulmonary atresia, Tricuspid atresia, Tricuspin stenosis)
  • Uhl disease
  • Ebstein anomaly
1735
Q

This refers to a heterogeneous group of congenital, non-sex-linked, genetic disorders of collagen type 1 production,involving connective tissues and bones. The hallmark feature is osteoporosis and fragile bones that fracture easily, as well as, blue sclera, dental fragility and hearing loss. Presence of ZEBRA STRIPE sign - cyclic bisphosphonate treatment produces sclerotic growth recovery lines in the long bones

A

Osteogenesis imperfecta

1736
Q

Complete vascular ring causes focal tracheomalacia or fixed tracheal stenosis. It is composed of what:

A
  • Right aortic arch and descending aorta
  • ARSA
  • LEFT ductus arteriosus or ligamentum arteriosum
1737
Q

This vascular anomaly has no symptoms ENT-wise (no stridor) or GI-wise (no dysphagia) BUT has decreased blood supply to UPPER EXTREMITY leading to DECREASED PULSES and ISCHEMIA of the extremity.

A

Isolated Left Subclavian Artery (ILSA)

While, Isolated Right Subclavian Artery (IRSA) findings are reversed from ILSA. They are like twins but different.

1738
Q

Vascular anomalies that pass anterior and compresses the trachea resulting in respiratory distress, wheezing, stridor, and difficulty in feeding. Tracheal indentation always ANTERIOR.

“AINNA & ALCCA are TROUBLESOME twins OUT FRONT, but ALLCA is CLOSEST to Archie.”

A

AINNA = Abberant INNominate Artery
ALCCA = Abberant Left Common Carotid Artery
OUT FRONT = Both pass ANTERIOR to trachea
TROUBLESOME = Tracheal compression, Respiratory distress, Wheezing, Stridor, Difficulty feeding
CLOSEST TO ARCHIE = ALCCA arises more PROXIMAL to AORTIC ARCH.

1739
Q

Most common cause of myocarditis

A

Viral, Coxsackie virus

1740
Q

Most common fetal cardiac tumor

A

Rhabdomyoma

1741
Q

This uterine mass causes abnormal bleeding by erosion of overlying endometrium. Compared to endometrial polyps, this uterine mass tends to be more hypoechoic, larger, and have multiple feeding vessels. Most common symptom is bleeding throughout the menstrual cycle. Acoustic shadowing may be seen emanating from the mass.

A

Submucosal Leiomyoma

1742
Q

Most common solid benign uterine neoplasm

A

Leiomyoma (Fibroids)

1743
Q

Ovarian epithelial tumor:
Thin-walled, usually unilocular, with anechoic fluid mimicking a functional ovarian cyst

A

Serous cystadenoma

1744
Q

Ovarian epithelial tumor:
Multiloculated with thick walls, thick septae and papillary projections into the fluid. On doppler study, blood flow is seen within the septa and papillary projections.

A

Serous cystadenocarcinoma

1745
Q

Ovarian epithelial tumor:
Maybe huge, filling the pelvis and extending high into the abdomen. Most have multiple septations and contain fluid that is echogenic because of the presence of MUCIN. Its rupture will spread mucin throughout the peritoneal cavity and may result in Pseudomyxoma peritonei.

A

Mucinous cystadenoma and cystadenocarcinoma

1746
Q

Polycystic ovary syndrome (PCOS)

A
  • Ovaries ENLARGED
  • Multiple follicles (>12 per follicle)
  • Follicles size < 10 cc with no dominant follicle >10 cc present
1747
Q

Serves as a sanctuary for disease because of ineffective access of chemotherapy

A

Testes

1748
Q

Presents on ultrasound as diffuse, punctate, non-shadowing, hyperechoic foci throughout the testicular parenchyma. Most patients have bilateral microlithiasis. It is a benign condition of microcalcifications within the seminiferous tubules but is associated with incidence of testicular carcinomas as high as 40%. Additional associations include cryptorchidism and infertility.

A

Testicular microlithiasis

1749
Q

Appear as mobile echogenic foci that move freely in the space between the layers of the tunica vaginalis. Most are small. Larger ones have been called “Scrotal pearls”. Cause is uncertain, possibly related to prior epididymitis. Incidental and of no clinical significance.

A

Scrotal calculi

1750
Q

Also known as lacunar skull or craniolacunae, is a dysplasia of the membranous skull vault and is associated with Chiari II malformations(seen in up to 80% of such cases). The inner table is more affected than the outer, with regions of apparent thinning (corresponding to unossified fibrous bone)of the skull vault. If particularly severe, with the individual lacunae coalescing into larger defects the term craniofenestrae is used.

A

Luckenschadel skull

1751
Q

Most common cause of symptomatic partial upper airway obstruction in infants

A

Croup

1752
Q

Most common cause of pulmonary infection in infants and young children

A

Respiratory syncytial virus

1753
Q

Most common cause of congenital bladder outlet obstruction

A

Posterior urethral valves

1754
Q

The most common extracranial solid childhood malignancy/neoplasm

A

Neuroblastoma

1755
Q

Most common chronic musculoskeletal disease of childhood

A

Juvenile idiopathic arthritis

1756
Q

Mri grade of stress injury:
- Perisoteal edema
- Mild bone marrow edema

A

Grade 2

1757
Q

Mri grade of stress injury:
- Periosteal edema
- Extensive bone marrow edema

A

Grade 2

1758
Q

Mri grade of stress injury:
- Periosteal edema
- Extensive bone marrow edema
- Multiple areas of intracortical changes / Fracture line

A

Grade IV

1759
Q

Refers to a depressed skull fracture of the infant skull caused by inner buckling of the calvarium. It is seen in newborns because of the soft and resilient nature of their bones (like greenstick fractures of long bones) and the fracture line is not visualized radiologically.

A

Ping pong skull fracture or pond skull fracture

1760
Q

First step in the orderly approach to the radiographic analysis of skeletal dysplasia

A

Assessment of Disproportion

1761
Q

Bone lesions that begin in the METAPHYSIS and with maturation , may migrate into diaphysis

A
  • Aneurysmal bone cyst
  • Chondromyoid fibroma
  • Enchondroma
1762
Q

Bone lesions arising from Metaphysis:
“S.O.F.A.CH.ER (sofachair) is Meta now. (Uso ngayon)”

A
  • SBC
  • Osteosarcoma
  • Fibrous dysplasia
  • ABC
  • osteoCHondroma
  • Enchondroma
1763
Q

Bone lesions arising from Diaphyses:
“DIA agents M.A.L.E O.fficers O.nly”

A
  • Multiple myeloma
  • Adamantimoma
  • Leukemia
  • Ewing sarcoma
  • O.steoid O.steoma
1764
Q

This sign refers to localized bilateral metaphyseal destruction of the medial proximal tibias. It is a pathognomonic sign of congenital syphilis.

A

Wimberger sign

1765
Q

This sign is a triangular or tubular echogenic cord of fibrous tissue, representing the ductal remnant of the extrahepatic bile duct,seen in the porta hepatis at ultrasonography, and is relatively specific for the diagnosis of biliary atresia.

A

Triangular cord sign

1766
Q

Most common type of tracheo-esophageal fistula

A

Proximal atresia with distal fistula (85%)

1767
Q

These are herniascontaining a Meckel diverticulum, and are also known as persistent omphalomesenteric duct hernias. They are most frequently encountered in the inguinal region. On CT scan, seen as a blind-ending tubular structure arising from antimesenteric border of small bowel and extending into inguinal sac. Normal appendix would be seen.

A

Littre hernia

1768
Q

Most common cause of small bowel obstruction in CHILDREN

A

Intussusception

1769
Q

The rarest among gastrointestinal duplications (<10%). Greater curvature is the most site of occurrence. Ultrasonography is an excellent imaging modality for characterization of these cystic masses. Often demonstate the typical “gut signature” or “double wall” sign

A

Gastric duplication cysts

1770
Q

The most common ingested foreign body

A

Coins

1771
Q

The most common cause of esophageal perforation in CHILDREN

A

Iatrogenic trauma

1772
Q

Primary imaging modality for the initial diagnosis of intussusception

A

Ultrasound

1773
Q

The most important factor that predicts unsuccessful enema reduction in Intussusception is

A

Longer duration of symptoms

(Bowels may be ischemic and/or infarcted after a long period of time. Can no longer be salvageable and must be removed surgically)

1774
Q

Type of choledochal cyst that presents with multiple cystic dilatation of both intra- and extrahepatic ducts.

A

Type 4

1775
Q

Most common malignancy of the spleen

A

Angiosarcoma

1776
Q

A syndrome of sequestration of blood elements within an enlarged spleen

A

Hypersplenism

1777
Q

Most common primary tumours of the spleen

A

Hamartoma & Hemangioma