Chung D H, Keum J S, Lee G K, Kim C J, Park S H
Department of Pathology, Capital Armed Forces General Hospital, Seoul National University College of Medicine, Korea.
J Korean Med Sci. 1995 Jun;10(3):211-5. doi: 10.3346/jkms.1995.10.3.211.
Spindle cell hemangioendothelioma is a rare vascular tumor which is presented with subcutaneous nodules and follows a benign indolent course but has a recurrent tendency, and is histologically resembling a cavernous hemangioma and Kaposi's sarcoma. We present a case of spindle cell hemangioendothelioma possessing clinical aggressiveness with painful bony erosion, histologic pleomorphism and mitoses. A 20-year-old man presented with a recurrent painful mass on the left ankle. The mass was dark brown and firm with irregular margins and measured 1.5 cm in diameter, which affected and eroded the underlying medial malleolus of the left tibia. Microscopically, the tumor was composed of cavernous endothelial-lined blood spaces and spindle cellular areas mimicking Kaposi's sarcoma. The spindle cells intermingled with plump epithelioid cells and showed a moderate degree of pleomorphism with occasional mitoses. Immunohistochemically, the spindle cells were focally positive for factor VIII-associated antigen and vimentin, and negative for S-100 protein, desmin, and epithelial membrane antigen.
梭形细胞血管内皮瘤是一种罕见的血管肿瘤,表现为皮下结节,病程呈良性、进展缓慢,但有复发倾向,组织学上类似于海绵状血管瘤和卡波西肉瘤。我们报告一例具有临床侵袭性的梭形细胞血管内皮瘤病例,伴有疼痛性骨质侵蚀、组织学多形性和核分裂象。一名20岁男性患者,左踝部有一复发性疼痛性肿块。肿块呈深褐色,质地硬,边缘不规则,直径1.5厘米,累及并侵蚀了左胫骨内踝。显微镜下,肿瘤由海绵状内皮衬里血腔和类似卡波西肉瘤的梭形细胞区域组成。梭形细胞与丰满的上皮样细胞混合,显示出中度多形性,偶见核分裂象。免疫组化显示,梭形细胞局部VIII因子相关抗原和波形蛋白呈阳性,S-100蛋白、结蛋白和上皮膜抗原呈阴性。