Chomette G, Auriol M, Guilbert F, Delcourt A
Pathol Res Pract. 1983 Aug;178(1):40-7. doi: 10.1016/S0344-0338(83)80083-1.
The ameloblastic fibrosarcoma is a rare variety of neoplasm. Three new cases reported here occurred within preexistent benign odontogenic tumors (ameloblastic fibroma or fibro-odontoma). These large, osteolytic tumors, spreading to adjacent soft parts, recurred after surgical treatment in two cases. One of them had a lethal course, with pleuro-pulmonary, mediastinal lymph node and hepatic metastases. Histologically, these sarcomas show a malignant mesenchymal component and few benign ameloblastic islands, which often disappear after one or several recurrences. Histoenzymologically, a high level of alkaline phosphatase and ATPase activities is always present, a feature not present in common fibrosarcomas. The ultrastructural study demonstrates, in analogy with odontogenic myxomas, clear cells provided with numerous microfilaments, secretory cells and also some fibroblasts and myofibroblast-like cells. In addition to these pleomorphic cells, a great number of peculiar granular cells with numerous lysosomal bodies were also found. The histogenesis of these tumors in unknown. Perhaps the epithelial component, being unable to assume its functions of organization, may initiate the malignant transformation of its odontogenic mesenchyme.
成釉细胞纤维肉瘤是一种罕见的肿瘤类型。本文报告的3例新病例发生于先前存在的良性牙源性肿瘤(成釉细胞纤维瘤或纤维牙瘤)内。这些巨大的溶骨性肿瘤可蔓延至相邻的软组织,2例经手术治疗后复发。其中1例病程凶险,出现胸膜肺、纵隔淋巴结和肝转移。组织学上,这些肉瘤表现为恶性间充质成分和少数良性成釉细胞岛,这些成釉细胞岛在一次或多次复发后常消失。组织酶学上,总是存在高水平的碱性磷酸酶和ATP酶活性,这一特征在普通纤维肉瘤中不存在。超微结构研究表明,与牙源性黏液瘤类似,有含大量微丝的透明细胞、分泌细胞,还有一些成纤维细胞和肌成纤维细胞样细胞。除了这些多形性细胞外,还发现了大量有许多溶酶体的特殊颗粒细胞。这些肿瘤的组织发生尚不清楚。也许上皮成分由于无法发挥其组织功能,可能引发其牙源性间充质的恶性转化。