Desbiens Christine, Hogue Jean-Charles, Lévesque Yves
Centre des Maladies du Sein Deschênes-Fabia, Hôpital du Saint-Sacrement, CHA Universitaire de Québec, 1050 chemin Sainte-Foy, Québec City, QC, Canada G1S 4L8.
Case Rep Oncol Med. 2011;2011:517047. doi: 10.1155/2011/517047. Epub 2011 Jul 6.
Background. Primary breast angiosarcoma is a rare entity. Case. Initial diagnosis was a benign hemangioma at core biopsy. Wide local excision was performed, with positive margins. Pathology after surgery reported a moderately differentiated angiosarcoma. Tumor was finally treated using mastectomy and radiations. She developed a second angiosarcoma in contralateral breast, with an initial diagnosis on core biopsy of an atypical vascular lesion and was again treated using mastectomy and radiations. She developed bones and lung metastases. Conclusion. Primary breast angiosarcoma is a rare entity often difficult to diagnose on core biopsy, and a benign differential diagnosis is frequent. A highly vascular breast mass should always be considered malignant until proven otherwise. Surgical treatment seems to be the best course of action. There is a lack of data proving efficacy of adjuvant chemotherapy and radiation therapy.
背景。原发性乳腺血管肉瘤是一种罕见的疾病。病例。粗针活检最初诊断为良性血管瘤。进行了广泛局部切除,切缘阳性。术后病理报告为中度分化血管肉瘤。肿瘤最终采用乳房切除术和放疗进行治疗。她对侧乳房出现了第二个血管肉瘤,粗针活检最初诊断为非典型血管病变,再次采用乳房切除术和放疗进行治疗。她出现了骨和肺转移。结论。原发性乳腺血管肉瘤是一种罕见的疾病,粗针活检时常常难以诊断,且经常需要与良性病变进行鉴别诊断。在排除其他可能之前,高度血管化的乳腺肿块应始终被视为恶性。手术治疗似乎是最佳的治疗方法。缺乏数据证明辅助化疗和放疗的疗效。