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先天性纤维肉瘤:存在组织细胞成分。

Congenital fibrosarcoma: presence of a histiocytic component.

作者信息

Gonzalez-Crussi F, Wiederhold M D, Sotelo-Avila C

出版信息

Cancer. 1980 Jul 1;46(1):77-86. doi: 10.1002/1097-0142(19800701)46:1<77::aid-cncr2820460116>3.0.co;2-z.

Abstract

We describe the histologic and ultrastructural appearance of a massive soft-tissue tumor in the left lower extremity of a newborn girl. In its clinical presentation and morphologic features, this tumor corresponded to the entity currently known as congenital fibrosarcoma. The variability of histologic conformation of these lesions is emphasized. Ultrastructural study disclosed many cells with the subcellular morphology of elements of the histiocytic-macrophagic series. Whether these cells are viewed as an integral part of the tumor or as a secondary feature, their presence in a congenital fibrosarcoma is of interest for understanding of biologic behaviour of these uncommon tumors.

摘要

我们描述了一名新生女婴左下肢巨大软组织肿瘤的组织学和超微结构特征。从临床表现和形态学特征来看,该肿瘤符合目前已知的先天性纤维肉瘤。强调了这些病变组织学结构的变异性。超微结构研究发现许多细胞具有组织细胞 - 巨噬细胞系列成分的亚细胞形态。无论这些细胞被视为肿瘤的一个组成部分还是次要特征,它们在先天性纤维肉瘤中的存在对于理解这些罕见肿瘤的生物学行为具有重要意义。

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