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患有进行性狼疮性肾炎或肺出血肾炎综合征的重症患者的治疗选择。

Therapeutic options for critically ill patients suffering from progressive lupus nephritis or Goodpasture's syndrome.

作者信息

Merkel F, Netzer K O, Gross O, Marx M, Weber M

机构信息

First Department of Internal Medicine, Klinikum Köln-Merheim, Cologne, Germany.

出版信息

Kidney Int Suppl. 1998 Feb;64:S31-8.

PMID:9475486
Abstract

Systemic lupus erythematosus is a chronic disease with many clinical features, while Goodpasture's syndrome usually becomes manifest with progressive glomerulonephritis and pulmonary hemorrhage. Rapidly declining renal function and even pulmonary hemorrhage may be the common feature. Early and precise diagnosis is most important as it may provide general prognostic information and serve as a guideline for initial therapy. Immunosuppression with oral cyclophosphamide and high dose corticosteroids together with plasmapheresis is used in Goodpasture's syndrome. Progressive lupus nephritis requires high dose corticosteroids together with i.v. pulses of cyclophosphamide for at least six months, followed by maintenance immunosuppression. The benefits of therapy must always be weighed against the risks. Nevertheless, current therapy remains less than optimal. A better understanding of the pathogenesis of systemic lupus erythrematosis (SLE) and Goodpasture's syndrome may provide more specific information about the nature and the role of the immune response and thus lead to new treatment strategies.

摘要

系统性红斑狼疮是一种具有多种临床特征的慢性疾病,而古德帕斯彻综合征通常表现为进行性肾小球肾炎和肺出血。肾功能迅速下降甚至肺出血可能是其共同特征。早期准确诊断最为重要,因为它可以提供总体预后信息,并作为初始治疗的指导。古德帕斯彻综合征采用口服环磷酰胺和大剂量皮质类固醇进行免疫抑制,并联合血浆置换。进行性狼疮性肾炎需要大剂量皮质类固醇联合静脉注射环磷酰胺脉冲治疗至少六个月,随后进行维持性免疫抑制。治疗的益处必须始终与风险相权衡。然而,目前的治疗仍不尽如人意。更好地理解系统性红斑狼疮(SLE)和古德帕斯彻综合征的发病机制可能会提供有关免疫反应的性质和作用的更具体信息,从而带来新的治疗策略。

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