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Papilliferous Keratoameloblastoma: A Rare Case Report

Ameloblastoma is true odontogenic tumor of epithelial origin, which is described as locally aggressive with varying chances of recurrence. It is believed to derive from enamel organ, remnants of dental lamina, lining of odontogenic cysts, or basal cells of oral epithelium. Radiologically, it may pre...

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Autores principales: Rathore, Ajit Singh, Juneja, Saurabh, Khurana, Neha, Shetty, Devi Charan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441264/
https://www.ncbi.nlm.nih.gov/pubmed/28584748
http://dx.doi.org/10.4103/ijabmr.IJABMR_136_16
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author Rathore, Ajit Singh
Juneja, Saurabh
Khurana, Neha
Shetty, Devi Charan
author_facet Rathore, Ajit Singh
Juneja, Saurabh
Khurana, Neha
Shetty, Devi Charan
author_sort Rathore, Ajit Singh
collection PubMed
description Ameloblastoma is true odontogenic tumor of epithelial origin, which is described as locally aggressive with varying chances of recurrence. It is believed to derive from enamel organ, remnants of dental lamina, lining of odontogenic cysts, or basal cells of oral epithelium. Radiologically, it may present as unilocular or multilocular radiolucency commonly. Although conventional ameloblastoma presents typical histological features as described by Vickers and Gorlin, few unusual variants have been reported with different histological patterns. However, the clinical and biological behavior of these lesser known variants has not been established yet due to the scarcity of cases reported. Here, we report an extremely rare case of papilliferous ameloblastoma in a young male patient with 2-year follow-up and presenting with unusual histological presentation than conventional ameloblastoma.
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spelling pubmed-54412642017-06-05 Papilliferous Keratoameloblastoma: A Rare Case Report Rathore, Ajit Singh Juneja, Saurabh Khurana, Neha Shetty, Devi Charan Int J Appl Basic Med Res Case Report Ameloblastoma is true odontogenic tumor of epithelial origin, which is described as locally aggressive with varying chances of recurrence. It is believed to derive from enamel organ, remnants of dental lamina, lining of odontogenic cysts, or basal cells of oral epithelium. Radiologically, it may present as unilocular or multilocular radiolucency commonly. Although conventional ameloblastoma presents typical histological features as described by Vickers and Gorlin, few unusual variants have been reported with different histological patterns. However, the clinical and biological behavior of these lesser known variants has not been established yet due to the scarcity of cases reported. Here, we report an extremely rare case of papilliferous ameloblastoma in a young male patient with 2-year follow-up and presenting with unusual histological presentation than conventional ameloblastoma. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5441264/ /pubmed/28584748 http://dx.doi.org/10.4103/ijabmr.IJABMR_136_16 Text en Copyright: © 2017 International Journal of Applied and Basic Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Rathore, Ajit Singh
Juneja, Saurabh
Khurana, Neha
Shetty, Devi Charan
Papilliferous Keratoameloblastoma: A Rare Case Report
title Papilliferous Keratoameloblastoma: A Rare Case Report
title_full Papilliferous Keratoameloblastoma: A Rare Case Report
title_fullStr Papilliferous Keratoameloblastoma: A Rare Case Report
title_full_unstemmed Papilliferous Keratoameloblastoma: A Rare Case Report
title_short Papilliferous Keratoameloblastoma: A Rare Case Report
title_sort papilliferous keratoameloblastoma: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441264/
https://www.ncbi.nlm.nih.gov/pubmed/28584748
http://dx.doi.org/10.4103/ijabmr.IJABMR_136_16
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