CVS Flashcards

1
Q

If you see nothing, look for…

A

amyloid

emboli

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2
Q

cardiomyopathies

A

hypertrophic/HOCM: all genetic (50% familial)

dilated: idiopathic, familial (25%), toxic, postviral, others
restrictive: ischaemic, amyloid, sarcoid

ARVD (familial) - fat in RV wall

left ventricular non-compaction - spongy LV wall

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3
Q

myocarditis (inflammatory cardiomyopathy)

A

lymphocytic (viral)

eosinophilic (hypersensitivity)

giant cell

granulomatous (exclude infection)

rheumatic fever

toxic (drugs)

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4
Q

cardiac valve vegetations

A

infective endocarditis

rheumatic heart disease

non-bacterial thrombotic endocarditis (no inflammation or destruction of valve)

Libman-Sacks endocarditis (SLE)

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5
Q

cardiac neoplasms

A

atrial myxoma (Carney complex)

rhabdomyoma (tuberous sclerosis)

cardiac sarcoma

lymphoma

mets

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6
Q

Beurger disease (clinical and morph)

A

young men, heavy smokers

small-medium arteries and veins of limbs

vasculitis with thrombotic occlusion

neuts and giant cell in thrombus

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7
Q

benign vascular tumours

A

capillary haemangioma (GLUT1+)

cavernous haemangioma/lymphangioma

arteriovenous malformation (thick and then vessels, A-V anastomoses, dx on arteriography)

epithelioid haemangioma (ALHE)

venous haemangioma

spindle cell haemangioma

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8
Q

capillary haemangioma subtypes

A

infantile: RICH, NICH (rapidly- or non-involuting congenital haemangioma)

tufted angioma

verrucous angioma

cherry angioma

pyogenic granuloma

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9
Q

intermediate vascular tumours

A

kaposiform HE (deep soft tissue infnants, assoc Kasabach-Merritt syndrome)

retiform HE (looks like rete testis, with hobnail cells)

Dabska tumour (papillary intralymphatic angioendothelioma)

KS (patch, plaque or nodular)

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10
Q

malignant vascular tumours

A

EHE

angiosarcoma (and epithelioid angiosarcoma)

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11
Q

reactive and ectatic vascular tumours

A

Masson tumour

glomeruloid haemangioma (Castlemans/POEMS)

port wine stain

venous lake

angiokeratoma

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12
Q

large (elastic) vessel vasculitis

A

giant cell arteritis

Takayasu arteritis (younger, more necrosis)

Both have granulomatous inflammation, use elastic stain in both

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13
Q

medium vessel vasculitis

A

1) Kawasaki disease (mucocutaneous lymph node syndrome): coronary artery in children, necrosis
2) polyarteritis nodosa: esp gut and kidney, fibrinoid necrosis
3) any of the small vessel vasculitides

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14
Q

fibrinoid necrosis in a vasculitis

A

polyarteritis nodosa

Wegeners

Churg-Strauss

rheumatoid vasculitis

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15
Q

pauci immune (no IgG on IF) small vessel vasculitis

A

Wegeners (respiratory tract, glomeruli): basophilic necrosis, giant cells, cANCA

Churg-Strauss (lungs, organs): palisading necrosis, eosinophils

microscopic polyangiitis (lungs, kidney): pANCA

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16
Q

immune mediated small vessel vasculitis (not distinguishable on histology - need clinical/serology). All have leukocytoclasis.

A

Henoch-Schonlein

cryoglobulinaemia

rheumatoid vasculitis

lupus vasculitis

17
Q

aortic valve stenosis

A

bicuspid AV

calcific aortic stenosis

post-inflammatory

post-rheumatic

18
Q

aortic valve insufficiency

A

1) root dilatation:

age related (minimal or no change)

bicuspid valve

Marfans

2) aortitis:

takayasu

giant cell arteritis

rheumatoid arteritis

syphilis

19
Q

mitral valve disease

A

stenosis: post inflammatory, post rheumatic

regurgitation:

1) mitral valve prolapse (myxoid degeneration) +/- Marfan or Ehlers-Danlos
2) annular dilatation (normal structure - caused by papillary muscle dysfunction in DCM or IHD)

20
Q

right side valve disease

A

congenital (eg ToF)

carcinoid heart disease

pulmonary artery hypertension

Fen-phen valvulopathy (anorectic drug)