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Int J Surg Case Rep. 2014;5(12):1142-4. doi: 10.1016/j.ijscr.2014.11.025. Epub 2014 Nov 13.

Ameloblastic fibro-odontoma.

International journal of surgery case reports

L K Surej Kumar, Suvy Manuel, Sherin A Khalam, Kannan Venugopal, T T Sivakumar, Jyothi Issac

Affiliations

  1. Department of Oral and Maxillofacial Surgery, PMS College of Dental Science and Research, Trivandrum, Kerala, India. Electronic address: [email protected].
  2. Department of Oral and Maxillofacial Surgery, PMS College of Dental Science and Research, Trivandrum, Kerala, India. Electronic address: [email protected].
  3. Department of Oral and Maxillofacial Surgery, PMS College of Dental Science and Research, Trivandrum, Kerala, India. Electronic address: [email protected].
  4. Department of Oral and Maxillofacial Surgery, PMS College of Dental Science and Research, Trivandrum, Kerala, India. Electronic address: [email protected].
  5. Department of Oral and Maxillofacial Pathology, PMS College of Dental Science and Research, Trivandrum, Kerala, India.
  6. Department of Pedodontics, PMS College of Dental Science and Research, Trivandrum, Kerala, India.

PMID: 25437658 PMCID: PMC4276268 DOI: 10.1016/j.ijscr.2014.11.025

Abstract

INTRODUCTION: Ameloblastic fibro-odontoma (AFO) is a quite rare, mixed odontogenic tumour generally seen in the early stages of life. Frequent signs of this tumour are asymptomatic swelling, delayed tooth eruption and mixed radiological appearance within well-defined borders. Management of the lesion includes enucleation of the tumour and long-term follow-up.

PRESENTATION OF CASE: A 10-year-old girl was referred to our oral and maxillofacial surgery clinic with an incidental radiological finding of radiopaque mass in the posterior region of maxilla. OPG showed unerupted tooth bud of upper right second molar and was being prevented from eruption by the odontome. Under general anaesthesia, the lesion was enucleated and the permanent right upper second molar tooth bud removed.

DISCUSSION: Mixed odontogenic tumours are a group of rare and interesting lesions which can mislead the clinician to variety of differential diagnosis. Adequate clinical and radiological investigations, proper surgical excison, accurate histopathological diagnosis, and long term follow up will ensure the right treatment plan for the patient.

CONCLUSION: The possibility of a mixed rare tumour should be kept in mind by the clinician where they deal with the swellings of posterior maxilla in children. Histological assessment revealed a final diagnosis of ameloblastic fibro-odontoma.

Copyright © 2014 The Authors. Published by Elsevier Ltd.. All rights reserved.

Keywords: Ameloblastic fibro-odontoma; Odontome; Posterior maxillary swelling mixed odontogenic tumours

References

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