IntroductionAmeloblastic fibroma (AF) is a rare, benign odontogenic tumor, accounting for approximately 1.5% to 4.5% of all odontogenic tumors. It was first described by Krause in 1891, but it was later recognized as a distinct entity by Thoma and Goldman in 1946.1 It is more commonly seen in children and adolescents, especially within the first two decades of life. There is a slight predilection for males,2 and the posterior mandible is the most frequent site of involvement. It is often associated with impacted or unerupted teeth.3Clinically, AF typically presents as a slow-growing, painless swelling, which may remain undetected until incidental discovery during routine radiographic examination. Radiographically, it often appears as a well-defined, unilocular or multilocular radiolucent lesion often with sclerotic radiopaque borders.1 Although considered benign, AF has the potential for recurrence and, in rare instances, malignant transformation into ameloblastic fibrosarcoma, emphasizing the importance of early diagnosis and appropriate management.Histopathologically, ameloblastic fibroma consists of both epithelial and connective tissue components. The epithelial component shows proliferating islands, cords, and strands of odontogenic epithelium with a peripheral layer of cuboidal or columnar cells and a central area resembling the stellate reticulum. The connective tissue component, resembling dental papilla, contains spindle and angular cells within a myxomatous stroma of delicate collagen. 2,3 Treatment options typically involve enucleation and curettage, surgical excision, partial resection and reconstruction. This case report discusses a rare presentation of ameloblastic fibroma in an 8-year-old female child, who presented with a painless swelling in the right posterior region of the mandible, which was histologically characterized by dentinoid formation.