Kahn L B, Webber B, Mills E, Anstey L, Heselson N G
Cancer. 1978 Aug;42(2):640-51. doi: 10.1002/1097-0142(197808)42:2<640::aid-cncr2820420235>3.0.co;2-m.
Seven cases of malignant fibrous histiocytoma of bone are documented. In addition to typical histologic features such as the presence of a storiform pattern, histiocytic and fibrocytic cell types and severe cellular atypism, in five cases there were areas in which osteoclast-type giant cells were prominent and the lesion resembled a giant cell tumor. Three of the seven patients developed pulmonary metastases within two years of amputation, one developed extensive local recurrence including soft tissue and vascular invasion, and the other three are without evidence of disease but have been followed for only short periods.
记录了7例骨恶性纤维组织细胞瘤。除了典型的组织学特征,如存在车辐状排列、组织细胞和纤维细胞类型以及严重的细胞异型性外,5例中还存在破骨细胞型巨细胞突出的区域,病变类似巨细胞瘤。7例患者中有3例在截肢后两年内发生肺转移,1例发生广泛的局部复发,包括软组织和血管侵犯,另外3例无疾病证据,但随访时间较短。