Aho A J, Aho H J
Pathol Res Pract. 1982 Jul;174(1-2):53-67. doi: 10.1016/S0344-0338(82)80028-9.
Ten cases of osteosarcoma were studied by electron microscopy. The tumors consisted of six cell types: fibroblastic, myofibroblastic, chondroblastic, osteoblastic, unclassified and histiocytic cells. Disturbed structure of dilated endoplasmic reticulum was a common feature. The neoplastic character of myofibroblastic and histiocytic cells is controversial. Myofibroblastic differentiation was most abundant in parosteal osteosarcoma and in fibrosarcomatous intraosseal osteosarcoma. The malignant cells sometimes formed giant cells and many aggregates of these cells were seen. Osteoclasts and other reactive cells were encountered and this may indicate host reaction against the tumor cells. Formation of collagenous and cartilaginous ground substance was poor, and the capacity of collagen to mineralize was decreased. It is concluded that osteosarcoma is the malignancy of a multipotential connective tissue cell which forms callus in normal osteogenesis.
通过电子显微镜对10例骨肉瘤进行了研究。肿瘤由六种细胞类型组成:成纤维细胞、肌成纤维细胞、软骨母细胞、成骨细胞、未分类细胞和组织细胞。扩张内质网的结构紊乱是一个常见特征。肌成纤维细胞和组织细胞的肿瘤性质存在争议。肌成纤维细胞分化在骨旁骨肉瘤和纤维肉瘤样骨内骨肉瘤中最为丰富。恶性细胞有时形成巨细胞,并且可见许多这些细胞的聚集物。遇到了破骨细胞和其他反应性细胞,这可能表明宿主对肿瘤细胞的反应。胶原和软骨基质的形成较差,并且胶原矿化的能力降低。结论是骨肉瘤是一种多能结缔组织细胞的恶性肿瘤,该细胞在正常骨生成中形成骨痂。