Taxy J B, Battifora H
Cancer. 1977 Jul;40(1):254-67. doi: 10.1002/1097-0142(197707)40:1<254::aid-cncr2820400138>3.0.co;2-w.
Sixteen cases of malignant fibrous histiocytoma are presented. Electron microscopy of 15 cases demonstrated fibroblast-like and mononuclear and multinucleated histiocyte-like cells. A small capillary was at the center of all storiform areas examined. Ultrastructural examination can be diagnostically useful within the context of a narrow differential diagnosis by conventional microscopy and the ability, by electron microscopy, to eliminate other mesenchymal cell types. In 13 cases, follow-up information was available from 18 months to 9 years following histological diagnosis. Five patients are alive and 8 patients have died, including two non-tumor related deaths. In 3 cases follow-up was less than 4 months. The biologic behavior of the tumor in this series was generally not related to histopathological parameters. The issue of histogenesis is largely unresolvable. Ultrastructural studies of various types of fibrous histiocytomas, suggesting cells of origin other than histiocytes, give credence to the concept that the histiocyte may represent a morphologic state of a given mesenchymal cell rather than a particular cell type.
本文报告了16例恶性纤维组织细胞瘤。15例的电子显微镜检查显示有成纤维细胞样、单核及多核组织细胞样细胞。在所检查的所有席纹状区域的中央均可见一条小毛细血管。在通过传统显微镜进行的鉴别诊断范围较窄且电子显微镜能够排除其他间充质细胞类型的情况下,超微结构检查对诊断可能有用。13例患者在组织学诊断后有18个月至9年的随访信息。5例患者存活,8例患者死亡(其中包括2例与肿瘤无关的死亡)。3例患者的随访时间不足4个月。该系列肿瘤的生物学行为通常与组织病理学参数无关。组织发生问题在很大程度上无法解决。对各种类型纤维组织细胞瘤的超微结构研究表明其细胞起源并非组织细胞,这支持了组织细胞可能代表特定间充质细胞的一种形态学状态而非一种特定细胞类型的概念。