Chen S H, Katayanagi T, Osada K, Hamano H, Inoue T, Shimono M, Takano N, Shigematsu T
Tokyo Dental College.
Bull Tokyo Dent Coll. 1991 May;32(2):51-6.
The present paper describes the relationship between ameloblastoma and ameloblastic fibroma deduced from a case diagnosed as "ameloblastoma combined with ameloblastic fibroma" arising in the mandible of a 5-year-old boy. Histologically, the tumor consisted of ameloblastoma in the central area and ameloblastic fibroma in the peripheral area; it clinically fits the characteristics of ameloblastic fibroma based on predominant age, manner of growth, and encapsulation. We reviewed the literature and discussed the relationship between ameloblastoma a ameloblastic fibroma in terms of tumorigenesis. It is assumed that ameloblastic fibroma can also be transformed into ameloblastoma, if the succeeding hard tissues are not formed, and the collagenous connective tissue substituting for the stromal mesenchymal tissue is formed by the inductive effect of the epithelial strands or other unknown factors. Several possibilities relative to the pathogenesis of ameloblastoma have been proposed by oral pathologists; however, to our knowledge, "ameloblastic fibroma can be transformed into ameloblastoma" has not hitherto been reported. The case we experienced here may be thought as an intermediate tumor pattern between ameloblastic fibroma and ameloblastoma.
本文描述了从一名5岁男孩下颌骨中诊断为“成釉细胞瘤合并成釉细胞纤维瘤”的病例推断出的成釉细胞瘤和成釉细胞纤维瘤之间的关系。组织学上,肿瘤中央区域为成釉细胞瘤,外周区域为成釉细胞纤维瘤;基于主要发病年龄、生长方式和包膜情况,其临床特征符合成釉细胞纤维瘤。我们回顾了文献,并从肿瘤发生学角度讨论了成釉细胞瘤和成釉细胞纤维瘤之间的关系。假定如果后续硬组织未形成,并且上皮条索或其他未知因素的诱导作用导致替代基质间充质组织的胶原结缔组织形成,成釉细胞纤维瘤也可转化为成釉细胞瘤。口腔病理学家已经提出了几种与成釉细胞瘤发病机制相关的可能性;然而,据我们所知,“成釉细胞纤维瘤可转化为成釉细胞瘤”迄今尚未见报道。我们在此遇到的病例可能被认为是成釉细胞纤维瘤和成釉细胞瘤之间的一种中间肿瘤模式。