Self Assessment Mock 2 Flashcards

1
Q

Best imaging for Popliteal artery entrapment syndrome

A

MRI - provides underlying anatomy and aids surgical planning

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2
Q

Amyloid arthropathy

A

Large joint, symmetrical arthropathy.
XR: Preserved joint space, subchondral cysts and well circumscribed erosions.
MRI: Low T1 and T2 intra-articular nodules and bone lesions with enhancement.
Positive on Congo Red stain

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3
Q

Scleroderma - oesophageal findings

A

Dilatation and reduced peristalsis in the distal 2/3 due to fibrosis of smooth muscle.
Upper oesophagus is unaffected.

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4
Q

Myositis ossificans

A

MRI: Low peripheral T1 and T2 with iso T1 and heterogenous T2 centrally.
Significant surrounding high STIR (oedema).
XR to confirm benign nature

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5
Q

Achondroplasia

A

Anterio-inferior beak and posterior vertebral vody scalloping (like Hurlers).
Narrowing of the interpedicular distance (like Thanatophoric)

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6
Q

Pyloric stenosis - US criteria

A

Single wall diameter >3mm,
Overall pyloric transverse diameter >11mm
Pyloric length >15mm,
Pyloric volume >1.5cc

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7
Q

Pituitary apoplexy

A

CT fairly insensitive
MRI: High T1 if haemorrhagic (depending on age of blood).
Peripheral enhancement with restricted diffusion in the infarcted centre.

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8
Q

Omphalocele vs Gastrochisis

A

Omphalocele is associated with Turners and other chromosomal abnormalities.
Omphalocele is midline and has peritoneal covering. Gastrochisis is right, has no covering or ascites.
Omphalocele is more associated with liver herniation and less with associated bowel complications

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9
Q

Loefgren syndome

A

Acute form of sarcoid with fevers, malaise, arthritis, lymph node enlargement and erythema nodosum.

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10
Q

Common cause for renal and splenic mets

A

Melanoma

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11
Q

ET tube placement in neonate

A

1.5cm above carina

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12
Q

TACE for HCC vs Thermal Ablation

A

Non-curative, life prolonging Rx for HCC.
Indicated for large, unresectable tumours with Child Pugh A and B.
Thermal ablation indicated for small tumours not amenable to surgery.
TACE can be used to reduce volume prior to thermal or used post thermal to reduce recurrence.

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13
Q

Osteitis Condensans Ilii

A

Benign, usually women with children.
Subchondral sclerosis, often triangular, at the iliac side of the SI joint with preserved joint space.

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14
Q

Pseudoprogression (chemo damage) vs Tumour Recurrence

A

MR Spect: Reduced Choline vs Reduced NAA and Increased Choline
CT perfusion: Reduced rCBV vs Increaseds rCBV
Thallium spect: Reduced vs Increased

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15
Q

Initial staging for SCC cervix

A

MRI pelvis and 18F-FDG PET/CT (Pet indicated for stage 2b or greater disease)

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16
Q

Mesenchymal hamartoma

A

Multiloculated cystic lesions with some vascular solid components and septae.
Similar appearance to infantile haemangioendothelioma but with normal aortic calibre
Normal AFP unlike hepatoblastoma

17
Q

Causes of increased liver attenuation

A

Haemochromatosis,
Amiodarone,
Thorotrast,
Iron overload,
Wilson disease,
Haemosiderosis,
Glycogen storage disease (can cause high or low)

18
Q

Causes of decreased liver attenuation

A

Fatty infiltration,
Amyloid,
Hepatic venous congestion,
Steroid use,
Glycogen storage disease (can cause high or low)

19
Q

Most common ILD associated with Sjogrens

A

NSIP
(Sjogrens is one of the only CTDs associated with LIP, but NSIP is still more common in Sjogrens)

20
Q

Tailgut cysts

A

Presacral space, high T2 and low T1 if simple, or can be complicated by infection, haemorrhage or mucus.
Lack of fat signal excludes endometrioma or dermoid.
Lack of sacral bone defect rules out anterior sacral meningocele

21
Q

Band heterotopia

A

Diffuse grey matter heterotopia affecting mostly females.
Band of grey matter deep to and roughly parallel to the cortex.

22
Q

Most powerful predictor of invasive adenocarcinoma (lung) vs AIS or MIA

A

Nodule mass

23
Q

Congenital rubella vs CMV

A

Rubella more associated with congenital cardiac abnormalities

24
Q

Glioblastoma

A

Complete rim enhancement, central fluid signal (necrosis), mild diffusion restriction and increased cerebral blood flow in and around the lesion

25
Kawasaki disease
Small or medium vessel vasculitis. Fever, rash, hand desquamation, red tongue, conjunctivitis, lynphadenopathy. Coronary artery aneurysms and thin walled, dilated GB are associated
26
Chordoma
Chordoma: Commonest primary sacral malignancy, also other midline structures. High T1 foci represent haemorrhage, fairly specific.
27
CXR findings in Truncus Arteriosus
Enlarged heart, plethoric lungs, left aortic arch. Associated with right arch in 1/3 of cases, more than background population but still left is more common.
28
Most common location for Meckels
Antimesenteric border of the distal ileum
29
GBM vs Lymphoma
Both cross the midline via corpus callosum. Lymphoma is uniformly enhancing and restricts diffusion. GBM is ring enhancing.
30
Lymphocele (post renal transplant)
Simple cystic structure adjacent to the kidney. Remains for years post op, in a well patient. Haematoma or seroma should have resolved by this time.
31
Chairi malformations
Chairi I: Just cerebellar tonsils inferiorly displaced. commonly incidental Chairi II: Varying severity. Small posterior fossa with descent of structures through foramen magnus, along with spinal myelomeningocele. Can include medulla and vermis herniation. Chairi III: more unusual, associated with encephaloceles.