Abstract
Post-breast cancer treatment-related angiosarcomas were first observed in lymphedematous extremities after mastectomy and are now being reported with increasing frequency after lumpectomy and radiation. A case history is presented of a BRCA2 carrier who had a postmastectomy chest wall angiosarcoma but had neither therapeutic radiation nor clinically evident lymphedema. The absence of established risk factors led to speculation that the BRCA2 germline mutation could be a causative factor in the development of this patient's angiosarcoma. A literature review supported this concept.
| Original language | English |
|---|---|
| Pages (from-to) | 533-537 |
| Number of pages | 5 |
| Journal | Clinical Breast Cancer |
| Volume | 8 |
| Issue number | 6 |
| DOIs | |
| State | Published - Dec 1 2008 |
Keywords
- Haploinsufficiency
- Loss of heterozygosity
- Lymphedema
- Radiation therapy
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