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肱骨非典型纤维组织细胞瘤:光镜与电镜研究

Atypical fibrous histiocytoma of the humerus: a light and electron microscopic study.

作者信息

Saito R, Caines M J

出版信息

Am J Clin Pathol. 1977 Sep;68(3):409-15. doi: 10.1093/ajcp/68.3.409.

Abstract

A unique osseous tumor, which arose in the humerus of a 44-year-old white man, is reported. The lesion was designated atypical fibrous histiocytoma because of the absence of atypical mitoses despite prominent nuclear pleomorphism of tumor cells. The tumor was composed mainly of spindle cells, tightly packed in a storiform pattern. Clear histiocytes and tumor giant cells were occasionally seen. Toward the proximal and distal ends, the tumor showed increasing fibrogenesis, and the ends were composed of areas of packed clear histiocytes and acellular myxoid matrix with focal calcification. Ultrastructurally, five cell types comprised the tumor, but fibroblast-like cells predominated. Histiocyte-like, xanthomatous, giant and undifferentiated cells were observed only occasionally. The patient has been followed for five years after disarticulation without developing evidence of distant metastasis.

摘要

报告了一例发生于一名44岁白人男性肱骨的独特骨肿瘤。尽管肿瘤细胞有明显的核多形性,但由于缺乏非典型有丝分裂,该病变被诊断为非典型纤维组织细胞瘤。肿瘤主要由梭形细胞组成,紧密排列成车辐状。偶尔可见透明组织细胞和肿瘤巨细胞。向近端和远端,肿瘤的纤维化逐渐增加,两端由密集的透明组织细胞区域和伴有局灶性钙化的无细胞黏液样基质组成。超微结构上,肿瘤由五种细胞类型组成,但以成纤维细胞样细胞为主。组织细胞样、黄色瘤样、巨细胞和未分化细胞仅偶尔观察到。该患者在关节离断术后随访了五年,未出现远处转移的证据。

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