Fukunaga M, Ushigome S
Department of Pathology, The Jikei University School of Medicine, Tokyo, Japan.
Virchows Arch. 1998 Oct;433(4):385-9. doi: 10.1007/s004280050264.
We report a Ewing-like adamantinoma of the periosteal region of the right tibia in a 15-year-old boy. The tumour was well demarcated but unencapsulated and showed cortical bone erosion. Histologically, the neoplastic cells were arranged in trabecular and cord-like patterns with fibrous, hyalinized, and myxoid stroma. Cellular atypia was mild, and mitotic figures were rarely seen. Many tumour cells expressed wide keratin, epithelial membrane antigen, leu 7, synaptophysin, Ewing's sarcoma-related antigen O13, and some were positive for neuron-specific antigen, vimentin, and CD68. The tumour was negative for S-100 protein, desmin, alpha-smooth muscle actin, and muscle-specific actin. Flow cytometric analysis showed that the tumour was aneuploid. After wide excision the patient has been well for the 16 months since diagnosis.
我们报告了一名15岁男孩右胫骨骨膜区域的尤文氏样造釉细胞瘤。肿瘤边界清晰但无包膜,表现为皮质骨侵蚀。组织学上,肿瘤细胞呈小梁状和索状排列,伴有纤维、玻璃样变和黏液样间质。细胞异型性轻微,罕见核分裂象。许多肿瘤细胞表达广谱角蛋白、上皮膜抗原、leu 7、突触素、尤文氏肉瘤相关抗原O13,部分细胞对神经元特异性抗原、波形蛋白和CD68呈阳性。肿瘤对S-100蛋白、结蛋白、α-平滑肌肌动蛋白和肌肉特异性肌动蛋白呈阴性。流式细胞术分析显示肿瘤为非整倍体。广泛切除术后,自诊断以来患者已健康存活16个月。