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心脏恶性纤维组织细胞瘤

Malignant fibrous histiocytoma of the heart.

作者信息

Terashima K, Aoyama K, Nihei K, Nito T, Imai Y, Takahashi K, Daidoji S

出版信息

Cancer. 1983 Nov 15;52(10):1919-26. doi: 10.1002/1097-0142(19831115)52:10<1919::aid-cncr2820521024>3.0.co;2-z.

Abstract

An autopsied case of malignant fibrous histiocytoma (MFH) in the left atrium of the heart of a 29-year-old Japanese woman was reported light and electron microscopically, and immunohistochemically. Metastasis was found in the adrenal, jejunum, and cervical regions. This is the fourth case of MFH of the heart in the literature. The tumor consisted of undifferentiated mesenchymal cells and histiocytoid cells, including giant cells and xanthomatous cells. Dense patches were commonly detected in all tumor cells. On frozen sections, histiocytoid cells formed EA and EAC rosettes, while fibroblastic cells formed EA rosettes only. Difference between them was also recognized in activity or amount of marker enzymes of histiocytes. These analyses suggested that MFH is a mesenchymal cell tumor with binary differentiation into histiocytoid cells and fibroblastic cells.

摘要

报告了一名29岁日本女性心脏左心房恶性纤维组织细胞瘤(MFH)的尸检病例,并进行了光镜、电镜及免疫组化检查。在肾上腺、空肠和颈部发现了转移灶。这是文献报道的第四例心脏MFH。肿瘤由未分化间充质细胞和组织细胞样细胞组成,包括巨细胞和黄色瘤细胞。在所有肿瘤细胞中均普遍检测到致密斑块。在冰冻切片上,组织细胞样细胞形成EA和EAC玫瑰花结,而成纤维细胞仅形成EA玫瑰花结。在组织细胞标记酶的活性或数量上也发现了它们之间的差异。这些分析表明,MFH是一种具有向组织细胞样细胞和成纤维细胞双向分化的间充质细胞肿瘤。

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