Stiller D, Katenkamp D
Zentralbl Allg Pathol. 1983;128(1-2):5-20.
Malignant fibrous histiocytoma of bone is a histologically well-defined tumor. Our aim is to describe five own cases and to analyze the published cases in order to demonstrate, the controversial aspects of clinical pathology. The essential histological criteria are the storiform tissue pattern and the presence of fibroblastic and histiocytic cells and giant cells. Inclusive of our cases, the total number reported stands at 196. There are features of malignant fibrous histiocytoma of bone about which there is almost general agreement: 1. The tumor occurs at all ages with an average onset from the age of 10 to the age of 50. 2. The tumor occurs in both the long and flat bones, but the main sites are the distal femur and the proximal tibia. 3. The tumor lacks any initial distinctive features in its clinical phase, but with respect to its biological behaviour, malignant fibrous histiocytoma of bone can be distinguished from osteosarcoma.
骨恶性纤维组织细胞瘤是一种组织学上定义明确的肿瘤。我们的目的是描述5例我们自己的病例,并分析已发表的病例,以展示临床病理学中存在争议的方面。基本的组织学标准是席纹状组织模式以及成纤维细胞、组织细胞和巨细胞的存在。包括我们的病例在内,报告的病例总数为196例。骨恶性纤维组织细胞瘤有一些几乎得到普遍认可的特征:1. 该肿瘤在各年龄段均可发生,平均发病年龄在10岁至50岁之间。2. 肿瘤可发生于长骨和平骨,但主要部位是股骨远端和胫骨近端。3. 该肿瘤在临床阶段缺乏任何初始的显著特征,但就其生物学行为而言,骨恶性纤维组织细胞瘤可与骨肉瘤相鉴别。