Srpski Arhiv za Celokupno Lekarstvo (Jan 2015)

Ameloblastic fibroma: A rare case report with 7-year follow-up

  • de Araújo Melo Leonardo,
  • Barros Adna Conceição,
  • de Cássia Santana Sardinha Sandra,
  • Cerqueira Arlei,
  • Nunes Dos Santos Jean

DOI
https://doi.org/10.2298/SARH1504190A
Journal volume & issue
Vol. 143, no. 3-4
pp. 190 – 194

Abstract

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Introduction. Ameloblastic fibroma (AF) is a rare benign odontogenic tumor that usually occurs in the first two decades of life. It affects adolescents and young adults and is found in the mandible and with a higher frequency in the posterior region of this segment. There are rare case reports with a long-term follow-up. Case Outline. We report the case of a 6-year-old boy with extensive ameloblastic fibroma in the mandible. Treatment consisted of enucleation and bone curettage, with the preservation of permanent teeth adjacent to the tumor. Clinical and radiographic follow-up of the patient over a period of 7 years showed no signs of recurrence or malignant transformation. Conclusion. Patients with AF should be under follow-up for prolonged periods of time, even in cases exhibiting a low proliferation index, because of the potential for recurrence and malignant transformation of this tumor.

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