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颗粒细胞瘤的组织发生——一项免疫组织化学和超微结构研究

Histogenesis of granular cell tumour--an immunohistochemical and ultrastructural study.

作者信息

Miettinen M, Lehtonen E, Lehtola H, Ekblom P, Lehto V P, Virtanen I

出版信息

J Pathol. 1984 Mar;142(3):221-9. doi: 10.1002/path.1711420309.

Abstract

Fifteen cases of granular cell tumour of superficial soft tissues or tongue were immunohistochemically evaluated for different types of intermediate filament proteins and for laminin, a glycoprotein of basal laminae. Four of the tumours were studied ultrastructurally. The tumour cells appeared to contain only vimentin-type of intermediate filament protein. The lobules of tumour cells were surrounded by laminin-positive material, but in contrast to schwannomas and neurofibromas, the individual tumour cells were not covered by laminin. In line with the immunohistochemical observations, by electron microscopy basal lamina-like material could not be demonstrated between individual cells, but only surrounding groups of cells. Lysozyme, a histiocytic marker, was absent in the tumour cells. Our results do not confirm any particular cell type for the histogenetic origin of granular cell tumour, but suggest that it may rather be derived from uncommitted possibly nerve-related mesenchymal cells.

摘要

对15例浅表软组织或舌部颗粒细胞瘤进行免疫组织化学评估,检测不同类型的中间丝蛋白以及基底膜糖蛋白层粘连蛋白。对其中4例肿瘤进行了超微结构研究。肿瘤细胞似乎仅含有波形蛋白类型的中间丝蛋白。肿瘤细胞小叶被层粘连蛋白阳性物质包围,但与神经鞘瘤和神经纤维瘤不同的是,单个肿瘤细胞未被层粘连蛋白覆盖。与免疫组织化学观察结果一致,电子显微镜检查显示,单个细胞之间未发现基底膜样物质,仅在细胞群周围发现。肿瘤细胞中不存在溶菌酶(一种组织细胞标志物)。我们的结果并未证实颗粒细胞瘤组织发生起源的任何特定细胞类型,而是提示它可能更源自未分化的、可能与神经相关的间充质细胞。

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