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This Journal feature begins with a case vignette highlighting a common clinical problem. Evidence supporting various strategies is then presented, followed by a review of formal guidelines, when they exist. The article ends with the authors' clinical recommendations.
A healthy 33-year-old woman comes to establish care. She reports no breast symptoms, her age at menarche was 14, and she has no children. She notes a family history of early-onset breast cancer in her sister (whose condition was diagnosed at the age of 35 years and who is alive at 39 years), mother (diagnosed at 37 years and alive at 60
The Clinical Problem
Strategies and Evidence
Risk Assessment and Genetic Testing
Specialized Breast-Cancer Surveillance
Breast Examination
Mammography
Magnetic Resonance Imaging
Ultrasonography
Screening for Other Cancers
Strategies for Reducing Risks
Chemoprevention
Surgery
Areas of Uncertainty
Recommendations from Professional Societies
Summary and Conclusions
Source Information
From the Clinical Genetics Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York.
Address reprint requests to Dr. Robson at the Clinical Genetics Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, 1275 York Ave., New York, NY 10021, or at robsonm@mskcc.org.
Related Letters:
Management of an Inherited Predisposition to Breast Cancer
Sardanelli F., Podo F., Robson M., Offit K.
Extract |
Full Text |
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N Engl J Med 2007;
357:1663, Oct 18, 2007.
Correspondence
This article has been cited by other articles:
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