Trassard M, Le Doussal V, Bui B N, Coindre J M
Département de Pathologie, Centre René Huguenin, Saint-Cloud, France.
Am J Surg Pathol. 1996 Nov;20(11):1412-7. doi: 10.1097/00000478-199611000-00014.
Angiosarcomas rarely develop within a peripheral nerve or a peripheral nerve sheath tumor. We describe an epithelioid angiosarcoma that arose in a benign schwannoma (neurilemoma) of the right thigh in a 65-year-old man who did not have von Recklinghausen's disease. Histologically, the resected tumor was a high-grade undifferentiated sarcoma that was predominantly arranged in solid sheets or nests and composed of epithelioid cells. The endothelial origin of the tumor was suggested by Factor VIII R-ag, Ulex europaeus-I, CD34, CD31, BNH9, and vimentin immunoreactivity, along with the ultrastructural evidence of occasional Weibel-Palade bodies. In this location, epithelioid angiosarcoma should be distinguished from malignant transformation of a schwannoma with epithelioid changes. This observation stresses the importance of immunohistochemical and ultrastructural analysis in the differential diagnosis of vascular tumors with features of epithelioid sarcoma.
血管肉瘤很少发生于周围神经或周围神经鞘瘤内。我们描述了一例上皮样血管肉瘤,该肿瘤发生于一名65岁男性右大腿的良性神经鞘瘤(神经膜瘤)中,该患者无冯雷克林霍增氏病。组织学上,切除的肿瘤为高级别未分化肉瘤,主要呈实性片状或巢状排列,由上皮样细胞组成。肿瘤的内皮起源通过因子VIII R-ag、荆豆凝集素-I、CD34、CD31、BNH9和波形蛋白免疫反应性得以提示,同时还有偶尔可见的W-P小体的超微结构证据。在此部位,上皮样血管肉瘤应与伴有上皮样改变的神经鞘瘤恶变相鉴别。该观察结果强调了免疫组化和超微结构分析在鉴别具有上皮样肉瘤特征的血管肿瘤中的重要性。