Altini M, Smith I
Int J Oral Surg. 1976 Jun;5(3):142-7. doi: 10.1016/s0300-9785(76)80063-4.
A rare case of ameloblastic dentinosarcoma is reported. The literature regarding ameloblastic fibro- and odontosarcomas is reviewed. There have been 16 reported cases of ameloblastic fibrosarcoma and another six cases (one uncertain) of ameloblastic fibrosarcoma which showed induction of dentin or enamel and which therefore according to the WHO Classification should be separately classified as ameloblastic odontosarcomas. Our case showed no enamel and therefore is better called ameloblastic dentinosarcoma. Ameloblastic sarcomas of the jaws are of low grade malignancy, do not often metastasize, and if treated by radical resection have a good prognosis.
本文报告了一例罕见的成釉细胞性牙本质肉瘤病例。对有关成釉细胞性纤维肉瘤和牙肉瘤的文献进行了综述。已有16例成釉细胞性纤维肉瘤的报告，另有6例（1例不确定）成釉细胞性纤维肉瘤显示有牙本质或釉质诱导，因此根据世界卫生组织分类应单独分类为成釉细胞性牙肉瘤。我们的病例未显示釉质，因此更好地称为成釉细胞性牙本质肉瘤。颌骨成釉细胞性肉瘤恶性程度低，不常发生转移，若行根治性切除，预后良好。
