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分子遗传学分析在肾细胞癌诊断中的应用。

The use of molecular genetic analysis in the diagnosis of renal cell carcinoma.

作者信息

Long J P, Anglard P, Gnarra J R, Walther M M, Merino M J, Liu S, Lerman M I, Zbar B, Linehan W M

机构信息

Urologic Oncology Section, Surgery Branch, National Cancer Institute, Bethesda, MD 20892.

出版信息

World J Urol. 1994;12(2):69-73. doi: 10.1007/BF00184239.

Abstract

The most common genetic aberration seen in nonpapillary renal cell carcinoma is believed to be the loss or inactivation of allelic material on the short arm of chromosome 3 (3p). Two patients underwent nephrectomy at our institution, each initially receiving a histologic diagnosis of renal cell carcinoma. Molecular analysis of these tissues revealed no genetic deletion on 3p, prompting further histologic and immunohistochemical evaluation of the original specimens. These additional studies confirmed alternate histologies other than renal cell carcinoma in each case. These data suggest that the loss of genetic material on the short arm of chromosome 3 may be specific for nonpapillary renal cell carcinoma. Molecular analysis may prove to be a useful adjunct in establishing the diagnosis in renal neoplasms with equivocal histologies.

摘要

非乳头状肾细胞癌中最常见的基因畸变据信是3号染色体短臂(3p)上等位基因物质的缺失或失活。两名患者在我们机构接受了肾切除术,最初均被组织学诊断为肾细胞癌。对这些组织进行的分子分析显示3p上没有基因缺失,这促使对原始标本进行进一步的组织学和免疫组化评估。这些额外的研究证实,在每例病例中,其组织学并非肾细胞癌。这些数据表明,3号染色体短臂上的基因物质缺失可能是非乳头状肾细胞癌所特有的。分子分析可能被证明是一种有用的辅助手段,用于对组织学不明确的肾肿瘤进行诊断。

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