Kale Saurabh Gajanan, Shetty Akshay, Balakrishnan Jintu, Purvey Praveen
Department of Oral and Maxillofacial Surgery, Sri Rajiv Gandhi College of Dental Sciences and Hospital, Bengaluru, Karnataka, India.
Department of Oral and Maxillofacial Pathology, Sri Rajiv Gandhi College of Dental Sciences and Hospital, Bengaluru, Karnataka, India.
Ann Maxillofac Surg. 2017 Jul-Dec;7(2):304-307. doi: 10.4103/ams.ams_84_17.
Ameloblastic fibro-odontoma (AFO) is a rare odontogenic tumor. Initially believed to be a lesion similar to ameloblastic fibroma (AF), it is now considered as a separate entity in the WHO odontogenic tumor classification. Commonly associated with a painless swelling and an associated absence of eruption of a tooth, AFO presents as a mixed radiopaque and radiolucent lesion in the younger population with a predilection for the posterior region. Histologically, it shows the characteristics of an immature complex odontoma with irregularly arranged enamel, dentinoid, cementoid-like structures, and ectomesenchymal tissue. The following case report describes a case of AFO with a predominantly radiopaque component and briefly discusses the available literature pertaining to this rare entity.
成釉细胞纤维牙瘤(AFO)是一种罕见的牙源性肿瘤。最初被认为是一种类似于成釉细胞纤维瘤(AF)的病变,现在在世界卫生组织牙源性肿瘤分类中被视为一个独立的实体。AFO通常与无痛性肿胀相关,且伴有牙齿萌出缺失,在年轻人群中表现为混合性的不透光和透光性病变,好发于后部区域。组织学上,它表现为不成熟复合牙瘤的特征,有不规则排列的釉质、类牙本质、类牙骨质样结构和外间充质组织。以下病例报告描述了一例以不透光成分为主的AFO病例,并简要讨论了有关这一罕见实体的现有文献。