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七例心脏黏液瘤的超微结构研究。

An ultrastructural study of seven cardiac myxomas.

作者信息

Feldman P S, Horvath E, Kovacs K

出版信息

Cancer. 1977 Nov;40(5):2216-32. doi: 10.1002/1097-0142(197711)40:5<2216::aid-cncr2820400532>3.0.co;2-h.

Abstract

Seven cardiac myxomas (CM) were studied by light and electron microscopy (EM) and their features compared with previously reported CM. Tumor cells were enmeshed within abundant stroma composed of fine electron dense granules. These cells were present either singly or more often in closely apposed small groups. The most distinctive ultrastructural feature in all seven CM was the presence of numerous cytoplasmic filaments. Our findings did not support a distinct separation into multiple cell types that could be clearly classified since the tumor cells had combined features of smooth muscle cells and fibroblasts. There has been no agreement on the principal cell type observed in CM, which has resulted in numerous theories about their histogenesis. Although the cell of origin of CM remains elusive, we fell that CM arise from primitive mesenchymal cells with multipotential capabilities for cell differentiation. Evidence is presented supporting the fact that CM are neoplasms and not thrombi. CM rarely recur but no bona fide metastasis has been reported.

摘要

对七个心脏黏液瘤(CM)进行了光镜和电镜研究,并将其特征与先前报道的心脏黏液瘤进行了比较。肿瘤细胞包埋于由细小电子致密颗粒组成的丰富基质中。这些细胞单个存在,或更常见地以紧密相邻的小群体形式存在。所有七个心脏黏液瘤最显著的超微结构特征是存在大量细胞质细丝。我们的研究结果不支持将其明确分为多种可清晰分类的细胞类型,因为肿瘤细胞具有平滑肌细胞和成纤维细胞的综合特征。关于在心脏黏液瘤中观察到的主要细胞类型尚无共识,这导致了关于其组织发生的众多理论。尽管心脏黏液瘤的起源细胞仍然难以捉摸,但我们认为心脏黏液瘤起源于具有多能细胞分化能力的原始间充质细胞。提供的证据支持心脏黏液瘤是肿瘤而非血栓这一事实。心脏黏液瘤很少复发,但尚未有真正转移的报道。

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