Vasculitis Flashcards

(36 cards)

1
Q

Two types of symptoms with vasculitis?

A
  • Non-specific systemic symptoms

* Symptoms of organ ischemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Large vessel vasculitis involves what

A

Aorta and major branches

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Two main types of large vessel vasculitis

A

Temporal (giant cell) arteritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Most common vasculitis in adults?

A

Temporal arteritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Temporal arteritis most commonly affects what?

A

Branches off the carotid artery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Symptoms of temporal arteritis?

A
  • HA
  • Visual disturbances
  • Jaw claudication
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Common lab finding in ESR

A

Very high ESR > 100

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are two ways that you can get ischemia secondary to vasculitis?

A
  1. Disrupt the endothelium → coagulation → thrombus

2. Injure wall → heal wall → fibrosis and narrowing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What will biopsy of temporal cell arteritis show?

A

Granulomatous inflammation (which shows giant cells) and intimal fibrosis (healing response)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is the distribution of inflammation in giant cell arteritis?

A

It is segmental

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How does Takayasu’s compare to giant cell arteritis?

A

Its almost the same except:
• Adults < 50 y/o (young Asian female)
• More proximal (aortic arch at branch points)
• Weak or absent pulses in upper extremity
• (will have elevated ESR and treat with steroids)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What arteries are involved in medium vessel vasculitis?

A

Muscular arteries supplying organs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is polyarteritis nodosa?

A

A NECROTIZING vasculitis that involved MOST organs but spares the LUNGS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Symptoms of polyarteritis nodosa?

A
  1. HTN (renal arteries)
  2. Abdominal pain with melena (mesenteric artery)
  3. Neurological distrubances
  4. Skin lesions
  5. Associated with serum HBsAG
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What type of necrosis is involved with polyarteritis nodosa?

A

Transmural fibrinoid necrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the common radiological finding in polyarteritis nodosa?

A

String of pearls appearance due to alternating segments of early fibrinoid necrosis and areas of fibrosis

17
Q

What disease commonly affects Asian children less than 4 years of age?

18
Q

What are early symptoms of Kawasaki’s disease?

A
Vague symptoms:
• Fever
• Conjunctivitis
• Erythematous rash on palms and soles
• Enlarged cervical lymph nodes
19
Q

What artery is preferentially involved with Kawasaki’s?

A

Coronary artery (can lead to MI or aneurysm

20
Q

What is Buerger disease?

A

Medium vasculitis involving the arteries of the hands which will present with ulceration, gangrene, and autoamputation of the hands.

21
Q

What is the treatment for Buerger disease

22
Q

What is Wegener’s granulomatosis?

A

Necrotizing granulomatous vasculitis of the nasopharynx, lungs, and kidneys

23
Q

Treatment for Wegeners

A

Cyclophosphamide

24
Q

High risk population for Wegeners

A

Middle aged male

25
Kidney involvement with Wegeners
Rapidly progressive glomerulonephritis
26
Serology for Wegeners
Elevated C-ANCA
27
What is microscopic polyangiitis?
Like Wegners but without nasopharyngeal involvement or granulomas
28
Serology for Microscopic polyangiitis?
Elevated P-ANCA
29
What is Churg-Strauss syndrome?
Necrotizing granulomatous vasculitis with eospinophilia which involved multiple organs including lungs and heart (differentiate this from microscopic polyangiitis)
30
How can you differentiate Churg-Strauss from microscopic polyangiitis since they both have p-anca
* Not granulomas with microscopic polyangiitis | * Churg-Strauss typically has asthma and eosinophilia
31
What is HSP?
Vasculitis from IgA and ICs deposition
32
What is most common vasculitis in kids?
HSP
33
What is rash like in HSP?
Palpable purpura in buttocks and legs
34
What are non-skin findings in HSP?
* Hematuria from IgA nephropathy | * GI pain and bleeding
35
When does HSP usually occur?
After a URI type infection (because you will get IgA production during URIs)
36
What is treatment for HSP?
Generally self-limited but can treat with steroids