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伴有t(X;17)的肾细胞癌:具有特定表型/基因型特征的罕见儿科肿瘤。

Renal cell carcinoma with t(X;17): singular pediatric neoplasm with specific phenotype/genotype features.

作者信息

Zambrano Eduardo, Reyes-Múgica Miguel

机构信息

Department of Pathology, Yale University School of Medicine, 310 Cedar Street, LB20, New Haven, CT 06520-8023, USA.

出版信息

Pediatr Dev Pathol. 2003 Jan-Feb;6(1):84-7. doi: 10.1007/s10024-002-1010-0. Epub 2002 Dec 10.

Abstract

Renal cell carcinomas in children are extremely rare and are usually associated with specific chromosomal rearrangements, different from those seen in adult patients. We present the case of a 9-year-old girl with a renal cell carcinoma with t(X;17) diagnosed at our institution. We also review the pertinent literature, with an emphasis on the genetic and molecular aspects associated with this rare neoplasm.

摘要

儿童肾细胞癌极为罕见,通常与特定的染色体重排相关,这与成年患者所见的情况不同。我们报告了一例在我院诊断为t(X;17)肾细胞癌的9岁女孩病例。我们还回顾了相关文献,重点关注与这种罕见肿瘤相关的遗传和分子方面。

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