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伴有颅骨发育不全的肾小管发育不全:两例报告

Renal tubular dysgenesis with hypoplastic calvaria: report of two cases.

作者信息

Erdogan S, Kacar A, Yilmazer D, Satar M, Tunali N

机构信息

Cukurova University, Medical Faculty, Department of Pathology, Adana, Turkey.

出版信息

Genet Couns. 2004;15(3):335-9.

Abstract

Renal tubular dysgenesis (RTD), a rare, lethal, autosomal recessive disorder, is characterized by short and poorly differentiated proximal tubules and associated with hypoplastic calvaria. We report two cases of RTD with hypoplasia of the calvaria. Microscopically, proximal tubules in the kidneys were not seen on routine H&E stain. Almost all tubules in the cortex were stained for epithelial membrane antigen (EMA), confirming the absence of proximal tubule differentiation. The autopsy findings, microscopic features and the etiology of this rare condition is discussed and compared with literature data.

摘要

肾小管发育不全(RTD)是一种罕见的致死性常染色体隐性疾病,其特征为近端小管短且分化不良,并伴有颅骨发育不全。我们报告两例伴有颅骨发育不全的RTD病例。显微镜下,常规苏木精-伊红(H&E)染色未在肾脏中发现近端小管。皮质中的几乎所有小管上皮膜抗原(EMA)染色阳性,证实近端小管未分化。本文讨论了这一罕见病症的尸检结果、微观特征及病因,并与文献数据进行了比较。

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