| Literature DB >> 27113794 |
Fahad Mujtaba Iqbal1, Balen Ahmed2, Raghavan Vidya2.
Abstract
Angiosarcomas are rare and aggressive malignant tumours of vascular or endothelial origin that can originate in the breast. They can be classified as primary or secondary, with the latter most commonly due to postoperative radiotherapy as part of breast conservation therapy (wide local excision and adjuvant radiotherapy) for breast cancer. We report a case of postirradiation secondary angiosarcoma in a 56-year-old woman, alongside a review of the current literature, to inform clinicians of its clinical presentation and characteristics as a high index of clinical suspicion is required for an accurate diagnosis. 2016 BMJ Publishing Group Ltd.Entities:
Mesh:
Year: 2016 PMID: 27113794 PMCID: PMC4854132 DOI: 10.1136/bcr-2016-215310
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X