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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)』 ■ウィキペディアで「Microscopic polyangiitis」の詳細全文を読む
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