Ameloblastic fibro-odontoma in children. Clinical aspects and review of the literature
Marcello Augello, Alessandro Rabufetti, Georges Ghazal and 2 more
Oral and Maxillofacial Surgery Cases · 2017
doi:10.1016/j.omsc.2017.01.001 (opens in a new tab)
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Abstract
The ameloblastic fibro-odontoma (AFO) is a rare mixed odontogenic tumor. Clinically AFO presents as a hamartoma or immature odontoma. The AFO is a well-encapsulated, painless, slow-growing and expanding tumor in young patients. Histologically, it has been classified as an ameloblastic fibroma or odontoma. Despite numerous efforts, there is still considerable confusion concerning the nature, the histology and the surgical therapy of this lesion. However, it can present with progressive growth causing bone destruction and significant deformity. The transformation of AFO in sarcoma is also known and extremely rare. Therefore a long term follow up is recommended. Enucleation still remains the gold standard. We are discussing our experience with AFO focused on children in clinical and surgical features and reviewing the relevant literature.
Abstract licence: CC BY-NC
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