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[伴有抗肾小球毛细血管基底膜抗体的快速进展性肾小球肾炎]

[Rapidly progressing glomerulonephritis with antibodies to glomerular capillary basement membrane].

作者信息

Matousovic K, Rossmann P

机构信息

Klinika nefrologie Institutu klinické a experimentální medicíny, Praha.

出版信息

Cas Lek Cesk. 1993 Mar 22;132(6):174-7.

PMID:8485756
Abstract

Antiglomerular basement membrane glomerulonephritis was diagnosed in 14 patients (6 men and 8 women) aged 20 to 59 years. Five patients were found to have Goodpasture s syndrome. 5 rapidly progressive glomerulonephritis. 1 nephrotic syndrome, and 1 had mild glomerulonephritis. Blood pressure, proteinuria and haematuria were not severe in most patients. In 10 patients, the diagnosis was not established before end-stage renal failure had developed. Four patients died of lung haemorrhage, in 3 the haemorrhage was controlled by the treatment, in 3 renal failure without lung haemorrhage occurred, and in 3 renal function improved or was stable. The prognosis improved significantly after plasma exchange together with immunosuppression had been introduced.

摘要

14例年龄在20至59岁之间的患者(6名男性和8名女性)被诊断为抗肾小球基底膜肾小球肾炎。其中5例患者患有Goodpasture综合征,5例为快速进行性肾小球肾炎,1例为肾病综合征,1例为轻度肾小球肾炎。大多数患者的血压、蛋白尿和血尿并不严重。10例患者在终末期肾衰竭发生之前未能确诊。4例患者死于肺出血,3例患者的出血通过治疗得到控制,3例发生了无肺出血的肾衰竭,3例患者的肾功能得到改善或保持稳定。在采用血浆置换联合免疫抑制治疗后,预后有了显著改善。

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1
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Cas Lek Cesk. 1993 Mar 22;132(6):174-7.
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