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恶性纤维组织细胞瘤的兴衰

The rise and fall of malignant fibrous histiocytoma.

作者信息

Erlandson Robert A, Antonescu Cristina R

机构信息

Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York 10021, USA.

出版信息

Ultrastruct Pathol. 2004 Sep-Dec;28(5-6):283-9. doi: 10.1080/019131290882150.

Abstract

The term malignant fibrous histiocytoma was coined by Stout and associates in the 1960s to encompass pleomorphic soft tissue sarcomas presumably derived from histiocytes that are capable of fibroblastic transformation. The concept was reaffirmed in the following 2 decades and malignant fibrous histiocytoma thus was regarded as the most common soft tissue tumor in older adults. However, recent more critical clinicopathologic, ultrastructural, and immunohistochemical studies have shown that malignant fibrous histiocytomas are not derived from histiocytic "facultative fibroblasts" and many neoplasms so diagnosed actually are pleomorphic subtypes of other sarcomas. Meticulous electron microscopic and immunohistochemical investigations also found that the more common storiform-pleomorphic, myxoid, and perhaps the giant cell subtypes are composed of variable mixtures of fibroblasts and phenotypically modulated fibroblastic cells, notably myofibroblasts and histiofibroblasts. On the basis of these findings, we propose a new classification for the above subtypes of so-called malignant fibrous histiocytoma, the majority of which are variants of pleomorphic fibrosarcoma.

摘要

“恶性纤维组织细胞瘤” 这一术语是由斯托特及其同事在20世纪60年代创造的,用于涵盖推测源自能够发生成纤维细胞转化的组织细胞的多形性软组织肉瘤。在随后的20年里这一概念得到了重申,因此恶性纤维组织细胞瘤被视为老年人中最常见的软组织肿瘤。然而,最近更为严谨的临床病理、超微结构和免疫组化研究表明,恶性纤维组织细胞瘤并非源自组织细胞性 “兼性成纤维细胞”,许多被诊断为此病的肿瘤实际上是其他肉瘤的多形性亚型。细致的电子显微镜和免疫组化研究还发现,更常见的席纹状多形性、黏液样以及可能的巨细胞亚型是由成纤维细胞和表型调节的成纤维细胞(特别是肌成纤维细胞和组织纤维母细胞)的不同混合物组成。基于这些发现,我们对上述所谓恶性纤维组织细胞瘤的亚型提出一种新的分类,其中大多数是多形性纤维肉瘤的变体。

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