Vasculitis Flashcards

1
Q

name the 5 main types of vasculitis

A
  1. large vessel
  2. medium vessel
  3. ANCA-associated small vessel
  4. immune complex small-vessel vasculitis
  5. anti-GBM
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2
Q

name the type of vasculitis:

polyarteritis nodosa
kawasaki disease

A

medium vessel

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3
Q

name the type of vasculitis:

microscopic polyangitis
Wegner’s
Churg-strauss

A

ANCA-associated small vessel

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4
Q

name the type of vasculitis:

cryoglobulinemic vasculitis
IgA vasculitis - Henoch-Schönlein
hypocomplementemic urticarial vasculitis - Anti-C1q vasculitis

A

immune complex small-vessel vasculitis

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5
Q

name the type of vasculitis:

Takayasu arteritis
giant cell arteritis

A

large-vessel

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6
Q

large vessel vasculitis affects what?

A

chronic granulomatous inflammation of the aorta and its major branches

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7
Q

name the 2 main types of large vessel vasculitis

A

GCA and Takayasu

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8
Q

who does Takayasu commonly affect?

age?
sex?
ethnicity?

A

young
female
asian

(100 times more common in asians)

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9
Q

GCA commonly affects what artery?

A

temporal artery

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10
Q

features of GCA?

A

low-grade fever, malaise, night sweats, weight loss, arthralgia and fatigue

claudicant symptoms

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11
Q

what 3 things are elevated in large vessel vasculitis?

A

ESR
PV
CRP

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12
Q

what imaging technique shows thickened walls and stenosis in large vessel arteritis?

A

MR angiography

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13
Q

large vessel arteritis treatment?

A

corticosteroids - 40-60mg prednisolone

methotrexate and azathioprine can be added

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14
Q

small to medium vasculitis can be split into what?

A

ANCA positive and negative

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15
Q

do small to medium vessel vasculitis blanch?

A

no

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16
Q

diagnose:

non-ANCA
IgA dominant

A

Henoch-Schnlein purpura

17
Q

diagnose:

ANCA
granulomatous
no asthma/eosinophilla

A

Wegner’s granulomatosis

18
Q

diagnose:

non-ANCA
no IgA
no cryoglobulinemia

A

other - IBD vasculitis

19
Q

diagnose:

ANCA
granulomatous
asthma/eosinophilla

A

Churg-Strauss Syndrome

20
Q

diagnose:

non-ANCA
no IgA
cryoglobulin

A

cryoglobulinemia

21
Q

diagnose:

ANCA
no granulomas

A

microscopic polyangitis

22
Q

the following may be seen in what condition:

fever and weight loss 
raised, non blanching purpuric rash 
arthralgia/arthritis 
mononeuritis multiplex 
glomerulonephritis 
lung opacities on x-ray
A

small-medium vessel vasculitis

23
Q

diagnose:

granulomatous inflammation involving the respiratory tract and necrotising vasculitis affecting small to medium vessels

A

granulomatosis with polyangitis (Wegner’s or GPA)

24
Q

diagnose:

necrotising vasculitis with few or no immune deposits affecting small vessels with glomerulonephritis being very common

A

microscopic polyangitis

25
diagnose: eosinophil-rich and granulomatous inflammation involving the respiratory tract and necrotising vasculitis affecting small to medium vessels associated with asthma and eosinophilia
Churg-Strauss Syndrome
26
GPA/Wegner's common symptoms?
ENT complications: nose bleeds, deafness, sinusitis, nasal crusting an nasal cartilage collapse, haemoptysis and caveating lesions on CXR
27
GPA is associated with _ANCA and PR_
GPA is associated with cANCA and PR3
28
EGPA/Churg-Strauss Syndrome characteristics?
late onset asthma, rhinitis and a raised peripheral blood eosinophil count neurological symptoms such as mono neuritis multiplex are common
29
most important complication in microscopic polyangitis?
glomerulonephritis
30
can ANCA be relied on all of the time for diagnosis?
no!
31
investigations of ANCA vasculitis?
``` ESR, PR, CRP anaemia U+E for renal ANCA urinalysis CXR biopsy ```
32
ANCA associated vasculitis treatment?
IV steroids and cyclophosphamide
33
name the generalised vasculitis that is non-ANCA and is IgA mediated
Henoch-Schonlein
34
who does Henoch-Schonlein commonly affect? after what infection?
childen | after URTI
35
Henoch-Schonlein signs/symptoms? treatment?
purpuric rash over the buttocks and lower limbs, abdominal pain and vomiting and joint pain self limiting - settles over weeks to months