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隆突性皮肤纤维肉瘤的组织发生。一项超微结构研究。

Histogenesis of dermatofibrosarcoma protuberans. An ultrastructural study.

作者信息

Alguacil-Garcia A, Unni K K, Goellner J R

出版信息

Am J Clin Pathol. 1978 Apr;69(4):427-34. doi: 10.1093/ajcp/69.4.427.

Abstract

Ultrastructural study of five typical lesions of dermatofibrosarcoma protuberans revealed that the basic cell is fusiform and has a somewhat indented nucleus and an even distribution of cytoplasmic organelles. Fragments of basal lamina, intercellular junctions, abundant intercellular fibers, and a tendency to form cellular sheaths also were found. The tumor cells had a strong resemblance to pericytes and perineural cells, as well as marked ultrastructural similarities to neurofibroma. The authors conclude that dermatofibrosarcoma protuberans arises from a primitive fibroblastic cell with a "sheath forming cell" differentiation that has a closer relationship to the perineural cell than to the pericyte.

摘要

隆突性皮肤纤维肉瘤五个典型病变的超微结构研究显示,基本细胞呈梭形,核稍凹陷,细胞质细胞器分布均匀。还发现了基底膜碎片、细胞间连接、丰富的细胞间纤维以及形成细胞鞘的倾向。肿瘤细胞与周细胞和神经周细胞非常相似,在超微结构上也与神经纤维瘤有明显相似之处。作者得出结论,隆突性皮肤纤维肉瘤起源于具有“鞘形成细胞”分化的原始成纤维细胞,与神经周细胞的关系比与周细胞的关系更密切。

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