首页> 外文期刊>Bulletin du Cancer: Journal de l'Association Francaise pour l'Etude du Cancer >HNPCC (hereditary non-polyposis colorectal cancer) or Lynch syndrome: a syndrome related to a failure of DNA repair system
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HNPCC (hereditary non-polyposis colorectal cancer) or Lynch syndrome: a syndrome related to a failure of DNA repair system

机译:HNPCC(遗传性非息肉性结直肠癌)或Lynch综合征:与DNA修复系统故障相关的综合征

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摘要

The HNPCC syndrome (hereditary non polyposis colon cancer) or Lynch syndrome stands for an autosomic dominant condition leading to the most prevalent hereditary colo-rectal cancers (CCR). MMR (mismatch repair)'s genes are involved in carcinogenesis as they play a role in ADNA mismatch repair. Microsatellite instability (MSI+ phenotype) induced by germline mutations is characteristic of such tumors and is necessary to assert the diagnosis. The HNPCC syndrome is associated with a significant increased risk of CCR altogether with endometrium, upper urinary tract and small bowel carcinomas as well as ovarian, biliary system and gastric cancers although of lesser extent. It is of importance to diagnose HNPCC syndrome prior to the treatment starts because it may influence patient's (as well as her/his relatives) disease management (type of surgery, surveillance and screening exams). New French recommendations, developed in 2009, about prophylactic colo-rectal and gynecologic surgeries and monitoring update latest ones published on 2004.
机译:HNPCC综合征(遗传性非息肉性结肠癌)或Lynch综合征代表常染色体显性遗传病,导致最普遍的遗传性结肠直肠癌(CCR)。 MMR(错配修复)基因参与ADNA错配修复,因此参与了癌变过程。种系突变引起的微卫星不稳定性(MSI +表型)是此类肿瘤的特征,是断言诊断所必需的。 HNPCC综合征与子宫内膜癌,上泌尿道癌和小肠癌以及卵巢癌,胆道癌和胃癌的CCR风险显着增加有关,尽管程度较小。在治疗开始之前诊断HNPCC综合征很重要,因为它可能影响患者(及其亲属)的疾病管理(手术类型,监视和筛查检查)。法国于2009年提出了有关预防性直肠和妇科手术和监测的最新法国建议,并于2004年发布了最新建议。

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