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并存的韦格纳肉芽肿病和抗肾小球基底膜病。

Coexistent Wegener's granulomatosis and anti-glomerular basement membrane disease.

作者信息

Wahls T L, Bonsib S M, Schuster V L

出版信息

Hum Pathol. 1987 Feb;18(2):202-5. doi: 10.1016/s0046-8177(87)80340-4.

Abstract

Wegener's granulomatosis and Goodpasture's syndrome represent two major causes of a pulmonary-renal syndrome. We describe the clinical course and morphologic features of a patient in whom pulmonary manifestations of Wegener's granulomatosis developed and were followed six months later by anti-glomerular basement membrane disease. Although we regard this as a unique and probably fortuitous association, a genetic predisposition or a secondary form of anti-GBM disease cannot be excluded.

摘要

韦格纳肉芽肿病和古德帕斯丘综合征是肺肾综合征的两大主要病因。我们描述了一名患者的临床病程和形态学特征,该患者先出现韦格纳肉芽肿病的肺部表现,六个月后又出现抗肾小球基底膜病。尽管我们认为这是一种独特且可能偶然的关联,但不能排除遗传易感性或抗肾小球基底膜病的继发形式。

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