Malignant nerve sheath tumor with rhabdomyoblastic differentiation arising from the acoustic nerve.

M Maeda, T Jozaki, S Baba, H Muro, H Shirasawa, T Ichihashi
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引用次数: 13

Abstract

A case of a malignant nerve sheath tumor with rhabdomyoblastic differentiation arising from the acoustic nerve in a 38 year old man is reported. At autopsy, the tumor was found to be extensively involved in the right cerebellopontine angle of the brain stem. Histologically, the tumor was composed mainly of spindle-shaped tumor cells proliferating in hypercellular fascicles scattered with pleomorphic cells. The tumor cells were characterized by high mitotic activity and invasive growth. Occasional tumor cells had eosinophilic cytoplasm, which in a few cases was cross-striated. Cytoplasmic interdigitations and a thick basal lamina were confirmed ultrastructurally. Immunohistochemical analysis revealed that some tumor cells were positive for myoglobin and desmin, but weakly positive or negative for S-100 protein. The patient did not have von Recklinghausen's disease.

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起源于听神经的恶性神经鞘肿瘤伴横纹肌母细胞分化。
我们报告了一位38岁男性听神经恶性神经鞘肿瘤伴横纹肌母细胞分化的病例。尸检发现肿瘤广泛累及脑干右桥小脑角。组织学上,肿瘤主要由纺锤形肿瘤细胞组成,呈高细胞束状,分散着多形性细胞。肿瘤细胞具有高有丝分裂活性和侵袭性生长的特点。偶尔肿瘤细胞有嗜酸性细胞质,少数呈横纹。细胞质间指和厚的基板在超微结构上被证实。免疫组化分析显示部分肿瘤细胞肌红蛋白和desmin阳性,但S-100蛋白弱阳性或阴性。这名患者没有患雷克林豪森氏病。
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