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Microscopic polyangiitis : ウィキペディア英語版
Microscopic polyangiitis

Microscopic polyangiitis (also known as microscopic polyarteritism,〔 "Microscopic polyarteritis nodosa," "MPA"〔) is an ill-defined autoimmune disease characterized by a systemic, pauci-immune, necrotizing, small-vessel vasculitis without clinical or pathological evidence of necrotizing granulomatous inflammation.
==Signs and symptoms==
Clinical features may include constitutional symptoms like fever, loss of appetite, weight loss, fatigue, and kidney failure. A majority of patients may have blood in the urine and protein in the urine. Rapidly progressive glomerulonephritis may occur. Because many different organ systems may be involved, a wide range of symptoms are possible in MPA.
Purpura and livedo racemosa may be present.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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