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Recurrent Ameloblastic Fibroma: Report of a Rare Case

Ameloblastic fibroma (AF) is an uncommon mixed neoplasm of odontogenic origin frequently seen in the second decade of life. It mainly presents as an intrabony lesion but can even occur peripherally. Histologically, our case showed hypercellular areas, an uncommon feature seen in typical AF. Whether...

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Detalles Bibliográficos
Autores principales: Kulkarni, Ravikumar S., Sarkar, Amitabh, Goyal, Sandeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673371/
https://www.ncbi.nlm.nih.gov/pubmed/23762647
http://dx.doi.org/10.1155/2013/565721
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author Kulkarni, Ravikumar S.
Sarkar, Amitabh
Goyal, Sandeep
author_facet Kulkarni, Ravikumar S.
Sarkar, Amitabh
Goyal, Sandeep
author_sort Kulkarni, Ravikumar S.
collection PubMed
description Ameloblastic fibroma (AF) is an uncommon mixed neoplasm of odontogenic origin frequently seen in the second decade of life. It mainly presents as an intrabony lesion but can even occur peripherally. Histologically, our case showed hypercellular areas, an uncommon feature seen in typical AF. Whether this benign lesion is treated by mode of enucleation and curettage or by extensive surgery is still a topic of debate. An extensive surgical treatment is suggested as the initial approach due to its high recurrence rate (18%) and the greater chances of recurrent AFs transforming into ameloblastic fibrosarcoma (45%), together with a long-term followup. We report a case of recurrent AF with hypercellular ectomesenchyme which developed a year after its conservative removal. We conclude that in recurrent AF sufficient sections of the pathological specimen are to be taken to rule out any malignant changes that might have begun in focal areas.
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spelling pubmed-36733712013-06-12 Recurrent Ameloblastic Fibroma: Report of a Rare Case Kulkarni, Ravikumar S. Sarkar, Amitabh Goyal, Sandeep Case Rep Dent Case Report Ameloblastic fibroma (AF) is an uncommon mixed neoplasm of odontogenic origin frequently seen in the second decade of life. It mainly presents as an intrabony lesion but can even occur peripherally. Histologically, our case showed hypercellular areas, an uncommon feature seen in typical AF. Whether this benign lesion is treated by mode of enucleation and curettage or by extensive surgery is still a topic of debate. An extensive surgical treatment is suggested as the initial approach due to its high recurrence rate (18%) and the greater chances of recurrent AFs transforming into ameloblastic fibrosarcoma (45%), together with a long-term followup. We report a case of recurrent AF with hypercellular ectomesenchyme which developed a year after its conservative removal. We conclude that in recurrent AF sufficient sections of the pathological specimen are to be taken to rule out any malignant changes that might have begun in focal areas. Hindawi Publishing Corporation 2013 2013-05-21 /pmc/articles/PMC3673371/ /pubmed/23762647 http://dx.doi.org/10.1155/2013/565721 Text en Copyright © 2013 Ravikumar S. Kulkarni et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kulkarni, Ravikumar S.
Sarkar, Amitabh
Goyal, Sandeep
Recurrent Ameloblastic Fibroma: Report of a Rare Case
title Recurrent Ameloblastic Fibroma: Report of a Rare Case
title_full Recurrent Ameloblastic Fibroma: Report of a Rare Case
title_fullStr Recurrent Ameloblastic Fibroma: Report of a Rare Case
title_full_unstemmed Recurrent Ameloblastic Fibroma: Report of a Rare Case
title_short Recurrent Ameloblastic Fibroma: Report of a Rare Case
title_sort recurrent ameloblastic fibroma: report of a rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673371/
https://www.ncbi.nlm.nih.gov/pubmed/23762647
http://dx.doi.org/10.1155/2013/565721
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