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A Case of Microscopic Polyangiitis / 대한신장학회잡지
Korean Journal of Nephrology ; : 358-362, 2000.
Article in Korean | WPRIM | ID: wpr-157722
ABSTRACT
Microscopic polyangiitis is a systemic small vessel vasculitis, which, although primarily associated with necrotizing and crescentic glomerulonephritis and pulmonary capillaritis, often has cutaneous and muscul-oskelectal features. Microscopic polyangiitis is strongly associated with antineutrophil cytoplamic autoantibody that are a useful diagnostic serologic marker for the most common form of necrotizing vasculitis, and that have two patterns(C-ANCA and P-ANCA). We have experienced a case of microscopic polyangiitis with purpurae on both lower extrimities, C-ANCA positive and cresent formation on renal biopsy, which had no history of asthma and no pathologic evidence of granuloma. In our case, deterioration of renal function was recovered after steroid pulse therapy.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Purpura / Asthma / Vasculitis / Biopsy / Antibodies, Antineutrophil Cytoplasmic / Microscopic Polyangiitis / Glomerulonephritis / Granuloma Language: Korean Journal: Korean Journal of Nephrology Year: 2000 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Purpura / Asthma / Vasculitis / Biopsy / Antibodies, Antineutrophil Cytoplasmic / Microscopic Polyangiitis / Glomerulonephritis / Granuloma Language: Korean Journal: Korean Journal of Nephrology Year: 2000 Type: Article