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核周型抗中性粒细胞胞浆抗体相关性血管炎和抗肾小球基底膜肾小球肾炎的序贯性发展

Sequential development of perinuclear ANCA-associated vasculitis and anti-glomerular basement membrane glomerulonephritis.

作者信息

Serratrice Jacques, Chiche Laurent, Dussol Bertrand, Granel Brigitte, Daniel Laurent, Jego-Desplat Sophie, Disdier Patrick, Swiader Laure, Berland Yvon, Weiller Pierre-Jean

机构信息

Service de Médecine Interne and Service d'Anatomie Pathologique, CHU Timone, Marseille, France.

出版信息

Am J Kidney Dis. 2004 Mar;43(3):e26-30. doi: 10.1053/j.ajkd.2003.11.019.

Abstract

A 75-year-old man suffered from perinuclear antineutrophil cytoplasm antibody (p-ANCA)-associated vasculitis with mild renal involvement. Three years later, he suddenly experienced an anuric acute renal failure due to anti-glomerular basement membrane (GBM) disease. Antibodies to myeloperoxydase were continuously present at a high titer in the patient's serum while serum anti-GBM antibodies were only detected at the time of the acute renal failure. A substantial proportion of patients with anti-GBM glomerulonephritis simultaneously display ANCAs whose pathogenic role is not clear. In our case, ANCAs were supposed to be of pathogenic importance because they may have uncovered the Goodpasture antigen. This case report lends further support to the concept that p-ANCA vasculitis may trigger anti-GBM disease.

摘要

一名75岁男性患有核周抗中性粒细胞胞浆抗体(p-ANCA)相关性血管炎,伴有轻度肾脏受累。三年后,他因抗肾小球基底膜(GBM)病突然出现无尿性急性肾衰竭。患者血清中髓过氧化物酶抗体持续高滴度存在,而血清抗GBM抗体仅在急性肾衰竭时检测到。相当一部分抗GBM肾小球肾炎患者同时表现出ANCA,其致病作用尚不清楚。在我们的病例中,ANCA被认为具有致病重要性,因为它们可能暴露了Goodpasture抗原。本病例报告进一步支持了p-ANCA血管炎可能引发抗GBM病这一概念。

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