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Primary Breast Angiosarcoma: A Case Report
Despoina Milonaki1, Natalia Sinou2, Nikoleta Sinou2
1Department of General Surgery, General Hospital of Nikaia "Agios Panteleimon", Athens, GRC.
None:
Primary breast angiosarcomas are extremely rare and aggressive tumors that originate from the inner lining of blood and lymphatic vessels in the breast. They are typically associated with a poor prognosis and have a strong tendency to metastasize. This report describes the case of a 57-year-old woman who detected a suspicious mass in her left breast during a routine self-examination. She initially underwent a lumpectomy, followed by a prophylactic mastectomy one year later. The tumor was identified as a well-differentiated primary breast angiosarcoma. The patient is currently being closely monitored and may require further treatment, including reconstructive surgery and adjuvant therapy. This case highlights the critical role of early detection and prompt intervention in enhancing the outcomes for patients with primary breast angiosarcomas. Despite their rarity, these tumors demand timely and comprehensive care to minimize the risk of recurrence and metastatic disease.
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