首页|期刊导航|外科理论与实践|遗传性乳腺癌风险基因检测与咨询:NCCN指南解读与瑞金医院临床实践

遗传性乳腺癌风险基因检测与咨询:NCCN指南解读与瑞金医院临床实践OACSTPCD

Hereditary breast cancer risk gene assessment and counseling:interpretation of NCCN guidelines and Ruijin Hos-pital clinical practice

中文摘要英文摘要

遗传性乳腺癌相关基因突变显著增加女性乳腺癌的发病风险,对此,美国国立综合癌症网络(NCCN)制定了《遗传/家族高风险评估指南》以指导这类基因突变携带者的遗传风险评估和咨询,为乳腺癌的预防、筛查和治疗提供必要信息.本文结合上海交通大学医学院附属瑞金医院的临床实践经验对《遗传/家族高风险评估指南》进行解读.

Hereditary breast cancer-related gene mutations significantly increase the risk of breast cancer in women.In this regard,the National Comprehensive Cancer Network(NCCN)Clinical Practice Guidelines in Genetic/Familial High-Risk Assessment was developed to guide genetic assessment and counseling in mutation carriers of breast cancer risk genes,providing crucial information for the prevention,screening and treatment of breast cancer.This article provided an interpretation of the NCCN Clinical Practice Guidelines in Genetic/Familial High-Risk Assessment,integrating the clinical practice experience of Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine.

韩梦圆;陈小松

上海交通大学医学院附属瑞金医院普外科 乳腺疾病诊治中心,上海 200025上海交通大学医学院附属瑞金医院普外科 乳腺疾病诊治中心,上海 200025

临床医学

乳腺癌遗传风险基因基因突变NCCN指南实践

Breast cancerHereditary risk geneGene mutationNCCN guidelinesPractice

《外科理论与实践》 2024 (5)

401-404,4

10.16139/j.1007-9610.2024.05.06

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