RITE Images 2003 Flashcards

1
Q
A

Axonal spheroids in diffuse axonal injury

“shear injury” -> immediately unconscious w/ trauma à chronic closed head injury

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2
Q
A

Pituitary adenoma

  • Not MEGS*
  • Meningioma ependymoma glioma Schwannoma*
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3
Q

Which cranial nerve would be involved?

A

Bony erosion involving the stylomastoid foramen -> CN7 involved

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4
Q
A

Cystic astrocytoma

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5
Q
A

FTD

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6
Q
A

Schwannoma of the vestibular branch of the 8th cranial nerve

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7
Q
A

14&6 Hz positive spikes best seen in referential montage

Seen in adolescents in the posterior regions during light sleep

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8
Q
A

Wilson’s

High signal intensity in Thalamus & Putamen

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9
Q
A

Cerebellar cystic hemangioblastoma

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10
Q
A

Subacute SDH w/ mass effect on ventricles -> surgery

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11
Q
A

Colloid cyst

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12
Q
A

NCS with temporal dispersion, conduction block, and slow conduction -> CIDP

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13
Q
A

AVM

Can do amytal test and intravascular embolization to make surgery & radiation therapy more effective

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14
Q
A

Arachnoid cyst

Patient presents with cluster headache -> breath oxygen rich mixture if HA were to return

Do not need to drain or decompress arachnoid cyst b/c there’s no mass effect

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15
Q
A

neurosarcoidosis

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16
Q
A

Congenital retinoblastoma

Pineal gland shouldn’t be calcified until age 2 -> pineoblastoma

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17
Q
A

ALS - Degeneration of the corticospinal tracts

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18
Q
A

Thrombosed superior saggital sinus

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19
Q
A

Intracranial hypotension secondary to persistent CSF leak

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20
Q
A

Epidural metastasis

Bone & inner table shows irregularity & infiltration of tumor into the epidural space (metastatic prostate CA)

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21
Q
A

Sleep spindles generated in the reticular thalamic nucleus

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22
Q
A

Trichinella organism acquired by ingestion of undercooked pork

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23
Q
A

Chiari malformation w/ syringomyelia

Can get hydrocephalus due to cerebellar tonsils protruding into the foramen magnum

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24
Q
A

Cryptococcus infection

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25
Q
A

No flow in basilar artery

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26
Q
A

Germinal matrix hemorrhage – complication of premature birth

Germinal matrix = located in walls of lateral ventricles – very vascular & delicate

4 subtypes

  • I – localized to germinal matrix
  • II – ruptured into ventricle w/o ventricular dilation
  • III – ruptured into ventricle WITH ventricular dilation
  • IV – ruptured into ventricle AND cerebral parenchyma
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27
Q

2 T2 images scanned 6 months apart

A

abnormal signal in GP & white matter disease adjacent to trigone of R lateral ventricle; cerebral atrophy & enlarged CSF spaces; ventricular & subarachnoid spaces have increased -> parenchymal tissue loss

Anoxic injury in GP –

If GP affected -> CHAMWA

Canavan’s & Krabbe’s – white matter lesions!

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28
Q
A

B symmetric, parasagittal, cortical & BG venous infarctions due to thrombosis of superior sagittal sinus & deep cerebral veins

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29
Q
A

Methotrexate neurotoxicity – multiple PERIVENTRICULAR discrete or confluent foci of necrosis in cerebral or spinal white matter

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30
Q
A

Tethered cord syndrome –

Pts w/
back pain,
thickened filum terminale,
widened SC,
Posterior lipoma
Low lying SC

Axial L1/L2 should only show you filum terminale & not cord

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31
Q
A

PICA infarct – occlusion of vertebral artery

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32
Q
A

Rosenthal fibers – Alexander’s Disease

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33
Q
A

Onion bulbs – demyelination & remyelination

Seen in:
CMT
CIDP
Dejerine Sottas
Refsum

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34
Q
A

Gray Matter heterotopia or heterotopic gray matter

35
Q
A

Aspergillosis -> hemorrhagic infarcts

36
Q
A

Dandy Walker Malformation

No vermis

No posterior corpus callosum

Large posterior fossa cyst

37
Q
A

No inferior vermis & hypoplasia of 2 cerebellar hemispheres

38
Q
A

Tabes Dorsalis

Paraneoplastic Panel

Vit E deficiency

Cu deficiency

39
Q
A

Canavan’s – U-fibers not spared

40
Q
A

Colloid cyst

41
Q
A

Cryptococcus – multiple bubbly cysts in white matter, caudate, & putamen

42
Q
A

NF1

43
Q
A

Subdural empyema

44
Q
A

Caudate – chorea

STN -> hemiballismus

SN -> PD

45
Q
A

Atrophic cerebellar vermis & loss of both Purkinje & Granule cell neurons -> alcoholic cerebellar degeneration

46
Q
A

Clivus chordoma – arise from embryonic notochord (mesodermal derivative)

3rd & 4th decades; extrapontine lesion

Cartilaginous tumors – 20-60YO; extradural, arise adjacent to body of sphenoid bone;

47
Q
A

Hamartoma in tuber cineureum - *pt would have precocious puberty

48
Q
A

Cavum septum pellucidum & cavum vergae

49
Q
A

lipoma

50
Q
A

ventriculitis

51
Q
A

MRI is effective in demonstrating a displaced optic chiasm b/c it’s mo

52
Q
A

Lateral Geniculate Nucleus (LGN)

53
Q
A

oligodendroglioma

54
Q
A
55
Q
A

Cyclopia - holoprosencephaly

56
Q
A

stroke

57
Q
A

NPH

58
Q

Tissue resected from intraventricular mass

A

Tuberous sclerosis

abundant eosinophilic cytoplasm w/ prominent single nucleoli – subependymal giant cell astrocytomas – SEGA!

59
Q
A

Healed toxoplasmosis – multiple calcified lesions seen in brain parenchyma, & cerebellum @ G/W junction – AIDS

AIDS patients have generalized atrophy

*Sarcoidosis – calcification is NOT a feature

Sturge-Weber – intracranial calcification 2ndary to pial angiomatosis w/ curvilinear calcification following contour of cortex typically in occipital / parieto-occipital lobe*

  • Hyperparathyroidism – B symmetric BG calcification, dentate nuclei of cerebellum & periventricular white matter*
  • Tuberous sclerosis – subependymal tubers lining ventricles*
60
Q
A

Flaky keratin – epidermoid/dermoid

61
Q
A

Neuritic plaques!

62
Q
A

GBM! Poorly circumscribed variegated mass w/ foci of necrosis & hemorrhage

NOT infarct, abscess, meningioma or Huntington’s

63
Q

What is disease?

Clinical presentation?

Treatment?

A

Tolosa-Hunt syndrome – enhancing lesion in cavernous sinus

Idiopathic noncaseating granulomatous inflammation in the cavernous sinus;

Acute painful ophthalmoplegia, progression over days to weeks, CN 3 & 6 involved; 4 & V1 in 1/3

Optic nerve 20%, V2 10%; may have elevated ESR & SLE; recurring attacks over months to eyars

Tx: high dose prednisone

64
Q
A

Small pons & cerebellar atrophy, & olive atrophy – cerebellar pontine olivary atrophy – look for loss of belly of pons!

65
Q
A

Severe pontine atrophy – olivopontocerebellar atrophy – part of MSA; alpha synuclein

66
Q
A

Schizencephaly w/ septo optic dysplasia – cavity lined w/ gray matter

Porencephalic cyst – cavity would be lined w/ white matter

67
Q
A

Tumor seeding – sagittal MR post gad who multiple round enhancing lesions on surface of spinal cord & dorsal aspect of upper thoracic cord

Cord contusions would have high signal intensity w/in the cord

68
Q
A

Hemosiderin from prior repeated SAH

69
Q
A

Centronuclear myopathy

Type I myofiber predominance

70
Q
A

Substantia nigra

Damage to one SN -> hemi parkinsonism contralateral to lesion

71
Q
A

Indusium griseum

Coronal section of CC & cingulate gyri

Indusium – direct continuation of hippocampal formation

72
Q
A

Thrombosed aneurysm

73
Q
A

Ill defined ring enhancement w/ edema -> malignant brain neoplasm

74
Q
A

Arnold Chiari Malformation – herniation of cerebellar vermis & medulla

kinking of upper cervical cord

beaking of quadrigeminal plate

75
Q
A

Anatomical variant of both ACA originating from LICA

RPCA originates from anterior circulation – (fetal origin)

76
Q
A

Negri body – eosinophilic intracytoplasmic inclusion in cortical neuron; seen in rabies

77
Q
A

Leigh’s disease – abnormal signal in brain stem & BG symmetric

-see metabolic acidosis & elevated lactate

78
Q
A

Ependymoma – b/c tumor arises from spinal canal & molds the vertebral bodies

Chordoma – arise FROM vertebral bodies or scrum

79
Q
A

Caudate atrophy

80
Q
A

Meningioma

Non contrast CT on L -> isointense extra-axial mass

Contrast enhancement is homogeneous & intense

81
Q
A

Dissection – flame shaped “stump” of ICA

82
Q

What is E?

A

E – superior medullary velum

thin, transparent lamina of white matter, which stretches between the superior cerebellar peduncles

It forms, together with the superior cerebellar peduncle, the roof of the upper part of the fourth ventricle

83
Q
A
84
Q
A

Quadrantic sectoranopia

stroke in the LGN

Anterior choroidal artery involved