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通过血浆置换和免疫抑制治疗非抗肾小球基底膜抗体介导的快速进展性肾小球肾炎。

Treatment of non anti-GBM-antibody mediated, rapidly progressive glomerulonephritis by plasmapheresis and immunosuppression.

作者信息

Müller G A, Seipel L, Risler T

出版信息

Klin Wochenschr. 1986 Mar 3;64(5):231-8. doi: 10.1007/BF01711654.

Abstract

A retrospective study was conducted to evaluate the efficacy of plasmapheresis in combination with different immunosuppressive drugs ("pulse" therapy, azathioprine or cyclophosphamide together with steroids) in nine patients presenting with rapidly progressive glomerulonephritis (RPGN) not mediated by antibody to glomerular basement membrane. Six of these patients had to be initially dialysed. All patients underwent renal biopsy, which revealed that seven patients had a minimum of 80% crescents and five had interstitial fibrosis. Recovery of renal function was observed in seven patients (78%). All patients without interstitial fibrosis were recompensated for at least 14 months after the acute onset of RPGN. Those who presented with interstitial fibrosis declined to endstage renal failure after 13 months requiring chronic hemodialysis treatment or cadaveric kidney transplantation. On the basis of these findings interstitial fibrosis seems to be a limiting factor for the prognosis of non-anti-GBM-antibody mediated RPGN.

摘要

开展了一项回顾性研究,以评估血浆置换联合不同免疫抑制药物(“冲击”疗法、硫唑嘌呤或环磷酰胺联合类固醇)对9例非抗肾小球基底膜抗体介导的快速进展性肾小球肾炎(RPGN)患者的疗效。其中6例患者最初需要进行透析。所有患者均接受了肾活检,结果显示7例患者至少有80%的新月体形成,5例有间质纤维化。7例患者(78%)肾功能恢复。所有无间质纤维化的患者在RPGN急性发作后至少14个月肾功能得到改善。那些出现间质纤维化的患者在13个月后进展为终末期肾衰竭,需要进行慢性血液透析治疗或尸体肾移植。基于这些发现,间质纤维化似乎是非抗GBM抗体介导的RPGN预后的限制因素。

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