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骨恶性纤维组织细胞瘤伴局灶性血管外皮细胞瘤样形态。

Malignant fibrous histiocytoma of bone associated with focal hemangiopericytomatous pattern.

作者信息

Terashima K, Suda A, Imai Y, Watanabe Y, Kasajima T, Matsuda M, Dobashi M

出版信息

Acta Pathol Jpn. 1981 Nov;31(6):1063-78. doi: 10.1111/j.1440-1827.1981.tb02018.x.

Abstract

A case of malignant fibrous histiocytoma of the tibia of a 49-year-old Japanese farmer was presented. The patient was diagnosed as malignant hemangiopericytoma by biopsy, whereas the amputated material showed a marked pleomorphism representing features of malignant fibrous histiocytoma. Ultrastructurally, undifferentiated mesenchymal cells, intermediate cells between the undifferentiated mesenchymal cells and fibroblastic cells, fibroblastic cells and histiocytoid cells including bizarre giant cells were confirmed in a broad modulating spectrum. The hemangiopericytomatous lesion was predominated by intermediate cells, the ultrastructure of which bore a close resemblance to that of pericytes, and was regarded to be resulted from a differentiation of undifferentiated mesenchymal cells towards the pericyte.

摘要

报告了一例49岁日本农民胫骨恶性纤维组织细胞瘤。患者活检诊断为恶性血管外皮细胞瘤,而截肢标本显示出明显的多形性,具有恶性纤维组织细胞瘤的特征。超微结构上,在广泛的调节谱中证实了未分化的间充质细胞、未分化间充质细胞与成纤维细胞之间的中间细胞、成纤维细胞和包括奇异巨细胞在内的组织细胞样细胞。血管外皮瘤样病变以中间细胞为主,其超微结构与周细胞极为相似,被认为是未分化间充质细胞向周细胞分化的结果。

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