How to spot heritable breast cancer: a primary care physician's guide

Cleve Clin J Med. 2014 Jan;81(1):31-40. doi: 10.3949/ccjm.81a.13051.

Abstract

Because breast cancer is common, primary care physicians will encounter many patients who have a personal or family history of it. Many patients may benefit from referral to a cancer genetics program for assessment, genetic counseling, and consideration of genetic testing. This article discusses the complexities of risk assessment in cancer genetics (focusing on breast cancer), and highlights the primary care physician's role in identifying and caring for patients at risk.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • BRCA1 Protein / genetics
  • BRCA2 Protein / genetics
  • Breast Neoplasms / diagnosis
  • Breast Neoplasms / ethnology
  • Breast Neoplasms / genetics*
  • Female
  • Genetic Counseling*
  • Genetic Predisposition to Disease
  • Genetic Testing*
  • Humans
  • Medical History Taking
  • Middle Aged
  • Physician's Role*
  • Practice Guidelines as Topic
  • Primary Health Care*
  • Risk Assessment

Substances

  • BRCA1 Protein
  • BRCA2 Protein