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丛状神经鞘瘤 被引量:2

Plexiform schwannoma:a case report
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摘要 报告1例丛状神经鞘瘤。患者男,74岁。因右胸部皮肤结节50年就诊。组织病理检查示真皮中散在分布多个大小、形态不一的肿瘤细胞团块,其周围有完整的包膜。肿瘤团块主要由许多梭形细胞组成,核深染,染色质丰富,有异形。免疫组化染色显示几乎所有肿瘤细胞的细胞核和细胞质S-100蛋白均阳性,而Ki-67阴性。符合丛状神经鞘瘤的诊断。组织病理上该病需与恶性周围神经鞘瘤鉴别。 A case of plexiform schwannoma is reported. A 74-year-old man presented with a 50-year history of nodule on his right chest. Histological examination showed muhinodular well-defined eneapsuled tumour masses of different sizes and shapes in the dermal. The tumor was composed of dense proliferation of chromatin-rlch spindle shaped cells with atypia nu- clei. Immunohistochemieal staining with anti-S-100 protein was positive in the nuclei and cytoplasm of nearly 100% of the tumor cells. Ki67 was negative. These findings were consistent with plexiform schwannoma. Differential diagnosis must be made with malignant peripheral nerve sheath tumour in histopathology.
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2009年第11期689-690,共2页 Journal of Clinical Dermatology
关键词 神经鞘瘤.丛状 schwannoma, plexiform
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  • 1Harkin J, Arrington JH, Reed R J, et al. Benign plexiform scbwannoma: a lesion dislinct from plexiform neurofibrnma[J]. J Neuropathol Exp Neurol, 1978, 37:622 (Abstract).
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  • 4Terasaki K, Mera Y, Uchimiya H, et al. Plexiform schwannoma [J]. Clin Exp Dermatol, 2003, 28(;4): 372-374.
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  • 6Kindblom LG, Ahlden M, Meis-Kindblom JM, et al. hnmunohistochemical and molecular analysis of p53, MDM2, proliferating cell nuclear antigen and Ki67 in benign and malignant peripheral nerve sheath tumours[J]. Virchows Arch, 1995, 427(1): 19-26.

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