梭形细胞血管内皮瘤附2例报告。

I Murakami, A B Sarker, N Teramoto, Y Horie, K Taguchi, T Akagi
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引用次数: 16

摘要

本文报告2例梭形细胞血管内皮瘤。其中一名患者为16岁的日本女性,自3岁起患有奥利氏病(多发性内生性软骨瘤病),11岁时右腿出现多发性SCH。梭形细胞血管内皮瘤病变与内生软骨瘤病发生部位重合,此后病变数量增加。这是奥利氏病合并多发性SCH的首次报道。另一名患者,一名33岁的日本女性,她是乙型肝炎病毒(HBV)的携带者,在右脚踝外侧出现孤立性SCH, 10年前切除了脂肪瘤。两例肿瘤细胞均由四种细胞类型组成:(i)梭形细胞;(ii)上皮样细胞;(iii)空泡内皮细胞;(iv)通常的内皮细胞。海绵状区内皮细胞和空泡细胞对欧洲巨藻凝集素1 (UEA-I)、因子viii相关抗原和波形蛋白有反应。梭形细胞和上皮样细胞只对波形蛋白起反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spindle cell hemangioendothelioma: a report of two cases.

Two cases of spindle cell hemangioendothelioma (SCH) are reported. One of the patients was a 16 year old Japanese female, who had been suffering from Ollier's disease (multiple enchondromatosis) since 3 years of age and had developed multiple SCH in the right leg at the age of 11 years. Spindle cell hemangioendothelioma lesions coincided with the site of enchondromatosis and increased in number thereafter. This is the first report of Ollier's disease complicated with multiple SCH. Another patient, a 33 year old Japanese female, who was a carrier of hepatitis B virus (HBV), developed solitary SCH in the lateral aspect of the right ankle where a lipoma was extirpated 10 years previously. Tumor cells of both cases were composed of four cell types: (i) spindle cells; (ii) epithelioid cells; (iii) vacuolated endothelial cells; and (iv) usual endothelial cells. Endothelia in the cavernous area and vacuolated cells reacted to Ulex europaeus agglutin 1 (UEA-I), factor VIII-related antigen and vimentin. Spindle cells and epithelioid cells reacted only to vimentin.

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