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Screening and diagnosis of endometrial cancer in Lynch syndrome

查看全文 作  者:Caroline [1]Cornou;Anne Sophie [1]Bats;Charlotte [1]Ngo;Léa [1]Rossi;Perrine [1]Capmas;Pierre Laurent-[1]Puig;Chérazade [1]Bensaid;Claude [1]Nos;Marie Aude Lefrère-[1]Belda;Fabrice [1]Lécuru 高影响力作者 机构地区:[1]Department of Gynecologic Oncology, European Hospital Georges Pompidou, University of Paris Descartes高影响力机构 出  处:《World Journal of Obstetrics and Gynecology》索引2016年第5卷第4期,共8页高影响力期刊 摘  要:Lynch syndrome(LS) is an autosomal dominant inherited cancer predisposition syndrome caused by a mismatch of DNA repair(MMR system). Lifetime risk of developing endometrial and ovarian cancer in LS is higher than in the general population and gynecologic screening appears interesting. Screening is based on several tests: pelvic ultrasound, endometrial biopsy and hysteroscopy for endometrial cancer, pelvic ultrasound and CA125 for ovarian cancer. Those tests appear efficient for the diagnosis of gynecologic cancers in LS. Nevertheless, screening tests have not proved clinical benefit until now, and potential problems of compliance, risk of false negative cases, and interval cancer associated with screening do justify offering prophylactic surgery to patients. Women with LS should be informed of the potential benefits and risks of screening and the importance of evaluation in case of gynecologic symptoms or abnormal bleeding. Chemoprevention by progestincontaining oral contraceptives and the treatment of premalignant lesion are available options for reducing the risk of endometrial cancer in LS population. 关 键 词:DNA修复 染色体 治疗方法 临床分析
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