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Peripheral ameloblastic fibrodentinoma in a 3-year-old boy: Report of an unusual and rare case

We report a rare and unusual case of a Peripheral Ameloblastic Fibro-Dentinoma (PAFD) occurring in a 3 year old Indian boy. The boy presented to the hospital complaining of swelling in anterior maxillary region with a history of trauma. Periapical radiography of the area did not reveal any bone reso...

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Autores principales: Kaur, Vaneet, Tilakraj, T N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917518/
https://www.ncbi.nlm.nih.gov/pubmed/29731567
http://dx.doi.org/10.4103/jomfp.JOMFP_118_17
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author Kaur, Vaneet
Tilakraj, T N
author_facet Kaur, Vaneet
Tilakraj, T N
author_sort Kaur, Vaneet
collection PubMed
description We report a rare and unusual case of a Peripheral Ameloblastic Fibro-Dentinoma (PAFD) occurring in a 3 year old Indian boy. The boy presented to the hospital complaining of swelling in anterior maxillary region with a history of trauma. Periapical radiography of the area did not reveal any bone resorption. The entire mass was excised under local anesthesia, and the histological examination revealed a diagnosis of PAFD. The postoperative course was satisfactory and the excised area has remained free of recurrence for 9 months. PAFD is a rare entity and only 5 cases have been reported in literature. The present case is one of the youngest in the group. The mode of differentiation of the odontogenic lesion is a pointer in the diagnosis and histogenesis has been discussed.
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spelling pubmed-59175182018-05-04 Peripheral ameloblastic fibrodentinoma in a 3-year-old boy: Report of an unusual and rare case Kaur, Vaneet Tilakraj, T N J Oral Maxillofac Pathol Case Report We report a rare and unusual case of a Peripheral Ameloblastic Fibro-Dentinoma (PAFD) occurring in a 3 year old Indian boy. The boy presented to the hospital complaining of swelling in anterior maxillary region with a history of trauma. Periapical radiography of the area did not reveal any bone resorption. The entire mass was excised under local anesthesia, and the histological examination revealed a diagnosis of PAFD. The postoperative course was satisfactory and the excised area has remained free of recurrence for 9 months. PAFD is a rare entity and only 5 cases have been reported in literature. The present case is one of the youngest in the group. The mode of differentiation of the odontogenic lesion is a pointer in the diagnosis and histogenesis has been discussed. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5917518/ /pubmed/29731567 http://dx.doi.org/10.4103/jomfp.JOMFP_118_17 Text en Copyright: © 2018 Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Kaur, Vaneet
Tilakraj, T N
Peripheral ameloblastic fibrodentinoma in a 3-year-old boy: Report of an unusual and rare case
title Peripheral ameloblastic fibrodentinoma in a 3-year-old boy: Report of an unusual and rare case
title_full Peripheral ameloblastic fibrodentinoma in a 3-year-old boy: Report of an unusual and rare case
title_fullStr Peripheral ameloblastic fibrodentinoma in a 3-year-old boy: Report of an unusual and rare case
title_full_unstemmed Peripheral ameloblastic fibrodentinoma in a 3-year-old boy: Report of an unusual and rare case
title_short Peripheral ameloblastic fibrodentinoma in a 3-year-old boy: Report of an unusual and rare case
title_sort peripheral ameloblastic fibrodentinoma in a 3-year-old boy: report of an unusual and rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917518/
https://www.ncbi.nlm.nih.gov/pubmed/29731567
http://dx.doi.org/10.4103/jomfp.JOMFP_118_17
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