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按癌症部位进行的基因检测:子宫。

Genetic testing by cancer site: uterus.

机构信息

Clinical Cancer Genetics Program, Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Cancer J. 2012 Jul-Aug;18(4):338-42. doi: 10.1097/PPO.0b013e3182610cc2.

Abstract

This review article discusses hereditary cancer predisposition syndromes with uterine manifestations. Lynch syndrome accounts for 2% to 3% of endometrial cancers. The identification of endometrial cancer patients at risk for Lynch syndrome is discussed, as are the characteristics of Lynch syndrome-associated endometrial cancer and the screening and prevention options for women at risk for Lynch syndrome-associated endometrial cancer. Endometrial cancer associated with PTEN hamartoma tumor syndrome (also known as Cowden syndrome) is also discussed. HLRCC (hereditary leiomyomatosis and renal cell carcinoma), which has an associated high risk of symptomatic uterine leiomyomas, is reviewed.

摘要

这篇综述文章讨论了具有子宫表现的遗传性癌症易感性综合征。林奇综合征占子宫内膜癌的 2%至 3%。讨论了识别有林奇综合征风险的子宫内膜癌患者的方法,以及与林奇综合征相关的子宫内膜癌的特征,以及有林奇综合征相关的子宫内膜癌风险的女性的筛查和预防选择。还讨论了与 PTEN 错构瘤肿瘤综合征(也称为考登综合征)相关的子宫内膜癌。综述了 HLRCC(遗传性平滑肌瘤和肾细胞癌),其与有症状的子宫平滑肌瘤的高风险相关。

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