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三例迟发性少肾单位肾发育不全。

Three cases of late-onset oligomeganephronia.

作者信息

Kawanishi Kunio, Takei Takashi, Kojima Chiari, Moriyama Takahito, Sugiura Hidekazu, Itabashi Mitsuyo, Tsukada Misao, Uchida Keiko, Honda Kazuho, Nitta Kosaku

机构信息

Department of Medicine, Kidney Center.

Department of Pathology , Tokyo Women's Medical University , Tokyo , Japan.

出版信息

NDT Plus. 2011 Feb;4(1):14-6. doi: 10.1093/ndtplus/sfq175. Epub 2010 Oct 12.

Abstract

Oligomeganephronia is classified as a subgroup of renal hypoplasia, characterized by histopathologic abnormalities which progress to end-stage renal disease (ESRD) by school age. We describe three adult cases of oligomeganephronia who have not yet developed ESRD. We performed a renal biopsy in all of them. The pathological features, consisting of a reduced number of enlarged glomeruli, were diagnostic of oligomeganephronia. It was assumed that the condition had not progressed to ESRD in the patients because the degree of loss of glomeruli may have been milder than that in typical cases of oligomeganephronia.

摘要

少肾小球肾发育不全被归类为肾发育不全的一个亚组,其特征是组织病理学异常,到学龄期会发展为终末期肾病(ESRD)。我们描述了三例尚未发展为ESRD的成年少肾小球肾发育不全病例。我们对所有患者都进行了肾活检。病理特征为肾小球数量减少且增大,这可诊断为少肾小球肾发育不全。据推测,这些患者的病情尚未发展为ESRD,是因为肾小球丧失的程度可能比典型的少肾小球肾发育不全病例要轻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/533d/4421621/df6ce088fef9/sfq175fig1.jpg

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