首页> 外文期刊>The journal of obstetrics and gynaecology research >Carcinoma of the lower uterine segment diagnosed with Lynch syndrome based on MSH6 germline mutation: A case report
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Carcinoma of the lower uterine segment diagnosed with Lynch syndrome based on MSH6 germline mutation: A case report

机译:基于MSH6种系突变的林奇综合征诊断术治疗患者的癌:案例报告

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Endometrial cancer in the lower uterine segment (LUS) is associated with Lynch syndrome with MLH1 or MSH2 germline mutation. Here, we report a case of carcinoma of the LUS diagnosed with Lynch syndrome based on MSH6 germline mutation in a 46-year-old woman with abnormal vaginal bleeding. She had had rectal cancer at age 39 with a family history of colon cancer (father, 75 years), pancreatic cancer (paternal grandmother, 74 years), and colon cancer (maternal grandmother, 85 years). Magnetic resonance imaging showed a tumor in the LUS. Endometrial biopsy revealed endometrioid adenocarcinoma G1. As her cancer history met the revised Bethesda criteria, we examined microsatellite instability and the result was negative, but loss of the MSH6 expression was detected by immunohistochemistry. Genetic testing revealed deleterious germline mutation of MSH6, which was compatible with Lynch syndrome. To our knowledge, this is the first case of endometrial carcinoma of the LUS with MSH6 germline mutation.
机译:下子宫段(LUS)中的子宫内膜癌与Lynch综合征与MLH1或MSH2种系突变有关。在这里,我们报告了基于MSH6种系突变在一个异常的阴道出血的46岁女性中被诊断出患有Lynch综合征的LUS的癌症案例。她在39岁时患有直肠癌,患有结肠癌(父亲,75岁),胰腺癌(祖母,74岁)和结肠癌(外祖母,85岁)的家族史。磁共振成像在LU中显示出肿瘤。子宫内膜活检显示腺瘤腺癌G1。随着她的癌症历史达到修订的贝塞斯达标准,我们检查了微卫星不稳定性,结果是阴性,但通过免疫组化检测MSH6表达的损失。基因检测揭示了MSH6的有害种类突变,与林奇综合征相容。据我们所知,这是具有MSH6种系突变的LU子宫内膜癌的第一种情况。

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