Sellke F W, Loughry C W, Kashkari S
Department of Surgery, Akron City Hospital, Ohio.
Int Surg. 1988 Jul-Sep;73(3):193-5.
Angiosarcoma of the breast is a rare mesenchymal malignancy with a poor prognosis. One hundred sixty-four cases have been reported in the literature with 19 five-year, and 7 ten-year disease-free survivals. Two new cases of angiosarcoma of the breast are presented here, with disease-free survivals of five and ten years. In most series reviewed, angiosarcoma of the breast demonstrates as a rapidly fatal disease. Because axillary lymph node metastasis is rare, simple mastectomy with wide surgical margins is the procedure of choice. The mammographic and histologic findings may appear deceptively benign. A correlation exists between the histologic characteristics and the prognosis. Although there have been reports of increased survival with Actinomycin D, adjuvant therapy has failed to significantly alter the course of the disease in most series.
乳腺血管肉瘤是一种罕见的间叶性恶性肿瘤,预后较差。文献报道了164例病例,其中19例有5年无病生存期,7例有10年无病生存期。本文介绍了2例乳腺血管肉瘤新病例,其无病生存期分别为5年和10年。在大多数回顾性系列研究中,乳腺血管肉瘤表现为一种迅速致命的疾病。由于腋窝淋巴结转移罕见,选择手术切缘广泛的单纯乳房切除术。乳房X线摄影和组织学表现可能看似良性。组织学特征与预后之间存在相关性。尽管有使用放线菌素D提高生存率的报道,但在大多数系列研究中,辅助治疗未能显著改变疾病进程。