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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

韩梦圆 陈小松

外科理论与实践2024,Vol.29Issue(5):401-404,4.
外科理论与实践2024,Vol.29Issue(5):401-404,4.DOI:10.16139/j.1007-9610.2024.05.06

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

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

韩梦圆 1陈小松1

作者信息

  • 1. 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
  • 折叠

摘要

Abstract

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.

关键词

乳腺癌/遗传风险基因/基因突变/NCCN指南/实践

Key words

Breast cancer/Hereditary risk gene/Gene mutation/NCCN guidelines/Practice

分类

医药卫生

引用本文复制引用

韩梦圆,陈小松..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[J].外科理论与实践,2024,29(5):401-404,4.

外科理论与实践

OACSTPCD

1007-9610

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