Ch 10: Blood Vessels Flashcards

1
Q

Immune mechanisms involved in vasculitis

A

1) deposition of immune complexes 2) direct attack on vessels by circulating Ab 3) Various forms of cell-mediated immunity

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2
Q

p-ANCAs are mainly against what ag?

A

MPO (myeloperoxidase)

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3
Q

c-ANCAs are mainly against what ag?

A

PR3 (proteinase 3)

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4
Q

Acute phase: Endothelial injury and denudation, ballooning degeneration of intimal smooth muscle cells & macrophages & medial smooth muscle cell necrosis, which may be fibrinoid.
Chronic phase: intimal hyperplasia and fibrosis of the vessel wall. Occasionally, vessels show complete fibrous occlusion.

A

Radiation Vasculitis

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5
Q

What are the Large vessel vasculitis diseases?

A
Giant Cell (temporal) Arteritis
Takayasu Arteritis
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6
Q

What are the medium vessel vasculitis diseases?

A

Polyarteritis Nodosa

Kawasaki Disease

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7
Q

What are the small vessel vasculitis diseases?

A

Microscopic Polyangitis
Granulomatosis w/ Polyangitis (Wegener’s)
Eosinophilic Granulomatosis w/ Polyangitis (Churg Strauss)
IgA Vasculitis (Henoch-Schonlein)

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8
Q

ANCA associated with Granulomatosis w/ Polyangitis (Wegener’s)

A

c-ANCA

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9
Q

ANCA associated with Microscopic Polyangitis

A

p-ANCA

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10
Q

ANCA associated with Eosinophilic Granulomatosis w/ Polyangitis (Churg-Strauss)

A

p-ANCA

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11
Q

Classic findings seen in Granulomatosis w/ Polyangitis

A

Sinusitis, hemoptysis w/ bilateral lung infiltrates, hematuria due to progressive glomerulonephritis

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12
Q

Classic findings seen in IgA Vasculitis (Henoch-Schonlen Purpura)

A

Palpable purpura on the buttocks and legs, GI Pain, hematuria (IgA Nephroathy)

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13
Q

Classic findings seen in Thromboangitis Obliterans (Buerger Disease)

A

Ulceration, gangrene and autoamputation of fingers and toes, Raynaud phenomenon is often present

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14
Q

Classic findings seen in Kawasaki Disease

A

Non-specific signs: fever, conjunctivitis, erythematous rash of palms and soles and enlarged cervical lymph nodes

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15
Q

Classic findings seen in Polyarteritis Nodosa

A

Seen in young adults w/ hypertension, abdominal pain w/ melena, neurologic disturbances and skin lesions

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16
Q

Classic findings seen in Eosinophilic Granulomatosis w/ Polyangitis (Churg- Strauss)

A

Asthama & peripheral eosinophilia

17
Q

Classic Findings seen in Microscopic Polyangitis

A

NO nasopharyngeal involvement of granulomas (differentiates from Wegeners)

Hemoptysis w/ bi-lateral lung infiltrates, hematuria due to progressive glomerulonephritis

18
Q

Classic Findings seen in Takayasu Arteritis

A

Present in adults ) in the upper extremity, ESR is elevated