Chapter 7 Vasculitis Flashcards

1
Q

What are two Large vessel vasculitides?

A

Temporal (Giant Cell) Arteritis

Takayasu Arteritis

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2
Q

What type of vasculitis is Temporal Arteritis? What vessel does it usually affect?

A

Granulomatous vasculitis that classically involves branches of the carotid artery.

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3
Q

What demographic does Temporal Arteritis affect?

A

Older adults (>50) usually women

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4
Q

What are the presenting symptoms of temporal arteritis?

A

Headache (temporal artery involvment), visual disturbances (opthalmic artery involvment), jaw claudication. FLu like symptoms with joint and muscle pain (polymyalgia rheumatica).

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5
Q

What is an irregular lab value seen in temporal arteritis?

A

ESR is elevated

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6
Q

What does a biopsy reveal in temporal arteritis? What is important to keep in mind when taking a biopsy segment?

A

Biopsy reveals inflamed vessel wall with giant cells and intimal fibrosis. Must take long segment because lesions are segmental.

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7
Q

What is the treatment of temporal arteritis. What major complication indicates early treatment even without confirmative diagnosis?

A

Treatment is corticosteroids. there is a high risk of blindness without treatment.

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8
Q

What type of vasculitide is takayasu Arteritis?

A

Large vessel granulomatous vasculitis very similar to temporal vasculitis.

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9
Q

What vessels does takayasu arteritis affect?

A

involves aortic arch at branch points.

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10
Q

What demographic does takayasu arteritis affect?

A

adults (<50) classically young asian females

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11
Q

What are the presenting symptoms of Takayasu arteritis?

A

visual and neurological symptoms with a weak or absent pulse in the upper extremity (pulseless disease)

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12
Q

What lab value is elevated in takayasu arteritis?

A

ESR

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13
Q

What is the treatment of takayasu arteritis?

A

Corticosteroids

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14
Q

Name 3 medium vessel vasculitides?

A

Polyarteritis nodosa
Kawasaki disease
Buerger Disease

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15
Q

What type of vasculitis is PAN? What type of arteries does it affect? which organs?

A

Medium vessel (muscular arteries supplying organs) necrotizing vasculitis. All organs except lungs.

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16
Q

How does PAN present?

A

In young adults as hypertension (renal artery involvment), abdominal pain with melena (mesenteric artery), neurological disturbances, and skin lesions.

17
Q

What virus is PAN associated with?

A

HBV

18
Q

What demographic does kawasaki disease affect?

A

Asian children <4

19
Q

How does kawasaki disease present?

A

Nonspecific signs including fever, conjuctivitis, erythematous rash of palms and soles, and enlarge cervical lymph nodes.

20
Q

What is a major feared complication of kawasakis disease (which artery)

A

Coronary artery involvment is common and leads to risk for thrombosis with MI and aneurysm with rupture

21
Q

How is kawasaki disease treated?

A

Aspirin and IVIG, disease is self limiting

22
Q

What doe early lesions of PAN show?

A

transmural inflammation with fibrinoid necrosis

23
Q

What type of vasculitis is buerger disease? what body parts does it affect?

A

medium vessel vasculitis involving digits.

24
Q

How does beurger disease present?

A

ulceration, gangrene, and autoamputation of fingers and toes, raynaud phenomenon is often present.

25
Q

What risk factor is high associated with beurger disease? what does treatment involve?

A

Smoking, treatment is to stop smoking

26
Q

What type of vasculitis is Wegners Granulomatosis (granulomatosis with polyarteriitis)? what areas of the body are commonly invovled?

A

necrotizing small vessel vasculitis involving the nasopharynx, lungs, and kidneys.

27
Q

What is the classic presentation of Wegners granulomatosis?

A

middle aged male with sinusitis or nasopharyngeal ulceration, hemoptysis with bilateral lung infiltrates, hematuria due to rapidly progressive glomerulonephritis. (presents with hematuria)

28
Q

What serum marker correlates with diease activity in Wegners granulomatosis?

A

c-ANCA

29
Q

What does biopsy reveal in Wegners granulomatosis?

A

Large necrotizing granulomas with adjacent necrotizing vasculitis

30
Q

What is the treament for Wegners granulomatosis? Does it work well?

A

cyclophosphamide and steroids, relapses are common

31
Q

What type of vasculitis is is microscopic polyangiitis? What organs does it involve?

A

Small vessel necrotizing vasculitis involving multiple organs, mainly lungs and kidney (similar to Wegners but without nasopahryngeal involvment)

32
Q

What serum marker correlates with disease activity in microscopic polyangiitis?

A

p-ANCA

33
Q

What type of Vasculitis is Churg-Strauss Syndrome and what organs does it primarily affect?

A

small vessel vasculitis with necrotizing granulomatous inflammation with eosinophils involving multiple organs especially the lungs and heart

34
Q

What findings are often present in Churg Strauss syndrome (clinical and laboratory)

A

Peripheral eosinophilia and asthma

35
Q

What serum marker correlates with disease activity in Churg strauss syndrome?

A

p-ANCA

36
Q

What type of vasculitis is Henoch schonlein purpura? what is the cause of it? what demographic is it most common in

A

Small vessel vasculitis due to IgA immune complex deposition mainly seen in children.

37
Q

How does Henoch Schonlein pupura present? what usually preceeds it?

A

palpable purpura on the buttocks and legs, GI pain and bleeding, and hematuria (IgA nephopathy) usually following an upper respiratory tract infection.

38
Q

How is Henoch schonlein purpura treated?

A

Disease is self-limited, but may recur; treat with steroids. if sever