Melo Filho Mário Rodrigues de, Pêgo Sabina Pena Borges, Cardoso Claudio Marcelo, Rocha Breno Amaral, Martelli-Júnior Hercílio, Flores Isadora Luana, Dos Santos Luis Antônio Nogueira, Paranaiba Livia Máris Ribeiro
Gen Dent. 2017 Nov-Dec;65(6):69-72.
An ameloblastic fibro-odontoma (AFO) is a rare mixed odontogenic tumor with histologic features of an ameloblastic fibroma in conjunction with the presence of dentin and enamel. It usually appears as a well-circumscribed radiolucency with radiopaque foci and slow growth and is commonly seen in children and young adults. A 13-year-old boy presented with an asymptomatic swelling in the posterior right region of the mandible and the right ascending ramus. The clinical, imaging, and histopathologic findings confirmed the diagnosis of an AFO. After 8 months, a radiolucent lesion involving the unerupted mandibular left third molar was observed; a final diagnosis of a dentigerous cyst (DC) was established for this lesion. Although coincidental events, metachronous odontogenic lesions suggest a possible common genetic origin, since both can be caused by related cellular signaling pathways. Complete enucleation is recommended for both AFOs and DCs; rates of recurrence are low.
成釉细胞纤维牙瘤(AFO)是一种罕见的混合性牙源性肿瘤,具有成釉细胞纤维瘤的组织学特征,并伴有牙本质和釉质。它通常表现为边界清晰的透射影,伴有不透射影灶,生长缓慢,常见于儿童和年轻人。一名13岁男孩在下颌骨右后区域和右升支出现无症状肿胀。临床、影像学和组织病理学检查结果确诊为AFO。8个月后,观察到一个涉及未萌出的下颌左第三磨牙的透射性病变;该病变最终诊断为含牙囊肿(DC)。尽管是同时发生的事件,但异时性牙源性病变提示可能存在共同的遗传起源,因为两者都可能由相关的细胞信号通路引起。对于AFO和DC,均建议进行完整摘除;复发率较低。