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一名特发性肾病综合征患儿的不寻常组织学表现。

Unusual histological findings in a child with idiopathic nephrotic syndrome.

作者信息

Springate James, Nadasdy Tibor

机构信息

Department of Pediatrics, School of Medicine and Biomedical Sciences, State University of New York, and Division of Nephrology, Women and Children's Hospital, Buffalo, NY, 14214, USA.

出版信息

Pediatr Nephrol. 2007 Mar;22(3):451-3. doi: 10.1007/s00467-006-0330-0. Epub 2006 Nov 1.

Abstract

We report a 2-year-old child with corticosteroid-resistant nephrotic syndrome whose renal biopsy revealed light microscopically normal glomeruli but highly unusual finger-like projections and arches of the glomerular basement membrane. To our knowledge, the association between nephrotic syndrome and this patient's rare ultrastuctural lesion has not been previously documented in the literature. It is not certain whether this basement membrane is pathogenic or a striking but coincidental developmental anomaly.

摘要

我们报告了一名患有皮质类固醇抵抗性肾病综合征的2岁儿童,其肾活检在光学显微镜下显示肾小球正常,但肾小球基底膜有极不寻常的指状突起和弓形结构。据我们所知,肾病综合征与该患者这种罕见的超微结构病变之间的关联此前在文献中尚无记载。尚不确定这种基底膜是致病性的,还是一种显著但巧合的发育异常。

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