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儿童和成人肾母细胞瘤共同发病机制的分子遗传学证据。

Molecular genetic evidence for common pathogenesis of childhood and adult Wilms' tumor.

作者信息

Kozman H M, Clarke J M, Little M H, Smith P J

机构信息

Queensland Institute of Medical Research, Herston, Brisbane, Australia.

出版信息

Cancer Genet Cytogenet. 1989 Mar;38(1):121-5. doi: 10.1016/0165-4608(89)90172-6.

Abstract

A case of Wilms' tumor in an adult is reported, showing, by restriction fragment length polymorphism analysis of somatic and tumor DNA, the loss of alleles from the short arm of chromosome 11. Loss of alleles in this region has previously been reported in childhood Wilms' tumor. The findings of this study indicate that adult Wilms' tumor and childhood Wilms' tumor may share a common pathogenic pathway. These results may also be useful in differentiating between Wilms' tumor and renal cell carcinoma or sarcoma in adults when the histologic findings are unclear.

摘要

报告了一例成人肾母细胞瘤病例,通过对体细胞和肿瘤DNA的限制性片段长度多态性分析显示,11号染色体短臂上等位基因缺失。此前在儿童肾母细胞瘤中也报道过该区域等位基因缺失。本研究结果表明,成人肾母细胞瘤和儿童肾母细胞瘤可能有共同的致病途径。当组织学检查结果不明确时,这些结果也可能有助于鉴别成人肾母细胞瘤与肾细胞癌或肉瘤。

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