Vasculitis Flashcards

(39 cards)

1
Q

general presentation of vasculitis

A

myalgia, arthralgia, arthritis, fever >38, wt loss, malaise

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2
Q

what is ANCA and what are the names of the types

A

Ab expressed by endothelium against neutrophil granulocyte

types: cytoplasmic, perinuclear

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3
Q

what test is used to detect ANCA

A

immunofluorescence

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4
Q

what does ANCA stand for

A

anti-neutrophil cytoplasmic ab

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5
Q

what score is used to monitor vasculitis

A

Birmingham vasculitis score

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6
Q

causes of secondary causes of vasculitis

A

infection, drug, toxin, inflammatory disorder e.g. cancer

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7
Q

broad categories of vasculitis

A

large vessel
medium vessel
small vessel

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8
Q

types of large vessel vasculitis

A

Takayasu arteritis

Giant cell arteritis

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9
Q

difference in age of presentation for large vessel vasculitis

A

Takayasu arteritis: <40yrs

Giant cell arteritis: >50yrs

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10
Q

condition associated with large vessel vasculitis

A

polymyalgia rheumatica

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11
Q

age, gender and race that are risk factors for takayasu’s arteritis

A

japanese female aged 20 - 40

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12
Q

general presentation of takayasu’s arterities

A

dizzy, vision change, weak arm pulses, weight loss, aortic regurg, HTN/IHD

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13
Q

blood tests for takayasu’s arteritis

A

ESR, CRP

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14
Q

imaging for takayasu’s arteritis

A

MRI / PET CT

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15
Q

management of takayasu’s arteritis

A

prednisolone

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16
Q

examples of medium vessel vasculitis

A

kawasaki’s disease, polarteritis nodosa PAN

17
Q

auto-antibody for kawasaki’s disease

vessels commonly affected by kawasaki’s disease

A

anti-endothelial ab

often coronary arteries

18
Q

age group affected by kawasaki’s disease

A

mainly children

19
Q

polyarteritis nodosa management

A

corticosteroids +- cyclophosphamide

20
Q

“necrotizing lesions, aneurysm, segmental transmural inflam + fibrinoid necrosis” describes pathology of which disease

A

polyartitis nodosa PAN

21
Q

categories of small vessel vasculitis

A

ANCA associated and immune complex

22
Q

examples of immune complex mediated small vessel vasculitis

A

cryoglobulinaemia, HSP, SLE, Goodpasture’s

23
Q

autoantibodies for GPA

A

cANCA, anti-PR3

24
Q

pathology of GPA

A

granulomatosis, necrotizing glomerulonephritis, retinal thrombosis

25
male, resp tract ulcer, sinusitis, nasal crust, epistaxis, deaf, otitis media, saddle nose, haemoptysis, cough, purpura, cranial nerve palsy, conjunctivitis, proptosis, uveitis
Wegener’s GPA polyangitis
26
investigations for GPA
CXR, urinalysis (proteinurea), autoantibodies
27
examples of anca associated small vessel vasculitis
wegener's GPA polyangitis microscopic polyangitis MPA churg strauss EGPA
28
autoantibodies for microscopic polyangitis mpa
pANCA, anti-MPO
29
microscopic polyangitis mpa pathology
necrotizing glomerulonephritis, no granulomas
30
what is pauci immune vasculitis
ANCA associated small vessel vasculitis
31
what is the difference between the presentation of GPA & EGPA
EGPA has later onset and asthma and no eye/ENT involvement
32
autoantibodies for EGPA
pANCA, anti-MPO
33
gender GPA more common in
males
34
what areas of the body are affected by PAN
at vessel bifurcation skin/gut/kidney, spares lung
35
what immune component is affected by Henoch-Schonlein purpura
IgA
36
age group affected by Henoch-Schonlein purpura
children, occasionally adults
37
predisposing factor sometimes present in HSP
strep URTI 1-3 weeks before
38
presentation of HSP
purpuric rash on feet / buttocks / extensor surfaces plus glumerulonephritis +- abdo pain
39
management of HSP
self limiting, supportive