Rosen P P
Am J Surg Pathol. 1985 Sep;9(9):652-8. doi: 10.1097/00000478-198509000-00004.
This report describes three female patients who were treated for diffuse vascular lesions of the breast. The lesion was congenital in one patient. Two were adults (40 and 59 years old). Each presented with a mass within the breast. Microscopically, the tumors were composed of vascular channels growing diffusely in breast parenchyma. The vessels were lined by flat, inconspicuous endothelium with sparse supporting mural tissue virtually devoid of smooth muscle. The lesions consisted of hemangiomatous (erythrocyte-containing) and lymphangiomatous (seemingly empty) channels with lymphoid aggregates. This combination of a mixed pattern of vessels and diffuse growth is similar to that seen in lesions that have been called angiomatosis in other anatomic sites. Because the microscopic distinction between very orderly angiosarcomas and angiomatosis may be difficult, complete excision of the tumor is necessary. For bulky lesions, this may require mastectomy. In one patient congenital angiomatosis has persisted and recurred twice in the mammary region over 39 years. The other two patients remain well 3 years after local excision and 2 years and 4 months after mastectomy, respectively. Angiomatosis of the breast has not exhibited clinically malignant behavior since no metastases have been observed.
本报告描述了三名接受乳腺弥漫性血管病变治疗的女性患者。其中一名患者的病变为先天性。另外两名是成年人(分别为40岁和59岁)。每位患者均表现为乳腺内有肿块。显微镜下,肿瘤由在乳腺实质中弥漫性生长的血管通道组成。血管内衬扁平、不明显的内皮细胞,几乎没有平滑肌的稀疏支持性壁组织。病变由含血管瘤性(含红细胞)和淋巴管瘤性(看似空的)通道以及淋巴样聚集物组成。这种血管混合模式和弥漫性生长与在其他解剖部位被称为血管瘤病的病变中所见相似。由于非常有序的血管肉瘤与血管瘤病在显微镜下可能难以区分,因此有必要完整切除肿瘤。对于体积较大的病变,这可能需要进行乳房切除术。一名患者的先天性血管瘤病持续存在,并在39年内在乳腺区域复发两次。另外两名患者分别在局部切除术后3年、乳房切除术后2年4个月情况良好。乳腺血管瘤病未表现出临床恶性行为,因为未观察到转移情况。