Gitelman综合征患者的C1q肾病。

NDT Plus Pub Date : 2011-12-01 Epub Date: 2011-09-06 DOI:10.1093/ndtplus/sfr097
Consolación Rosado Rubio, Pilar Fraile Gómez, María Asunción Gómez Muñoz, Pedro Garcia-Cosmes, José Luis Lerma Márquez
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引用次数: 3

摘要

巴特综合征可以表现为三种不同的形式,很少与肾小球肾病合并。然而,这种关联在儿童中更为常见。我们报告的情况下,一个50岁的妇女与吉尔曼综合征在过去的30年谁也有最近出现的肾病综合征。她的肾活检显示肾小球旁器官增生和肾小球系膜C1q沉积,无系统性红斑狼疮的临床或血清学证据。我们尚未发现成人患者C1q肾病引起的Gitelman综合征和肾病综合征的相关报道。本病例提示低钾血症小管肾病与肾小球肾病之间可能存在关联,后者可引起肾病综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

C1q nephropathy in a patient with Gitelman syndrome.

C1q nephropathy in a patient with Gitelman syndrome.

C1q nephropathy in a patient with Gitelman syndrome.

Bartter syndrome can manifest in three different forms and is rarely concomitant with glomerular nephropathies. However, this association is more frequently observed in children. We report the case of a 50-year-old woman with Gitelman syndrome for the past 30 years who also had a nephrotic syndrome of recent appearance. Her renal biopsy revealed hyperplasia of the juxtaglomerular apparatus and mesangial deposits of C1q, with no clinical or serological evidence of systemic erythematous lupus. We have not found any reports of instances of association of Gitelman syndrome and nephrotic syndrome arising from C1q nephropathy in adult patients. Our case suggests the possible existence of an association between hypokalaemic tubular nephropathies and glomerular nephropathies that may cause nephrotic syndrome.

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