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Papilliferous Keratoameloblastoma: An Extremely Rare Case Report

Odontogenic tumors develop in the jaw bones from the odontogenic tissue-oral epithelium in tooth germ, enamel organ, dental papilla, reduced enamel epithelium, remnants of Hertwig's root sheath or dental lamina, and so forth. Hence, a bewildering variety of tumors are encountered in the maxilla...

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Autores principales: Mohanty, Neeta, Rastogi, Varun, Misra, Satya Ranjan, Mohanty, Susant
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3686074/
https://www.ncbi.nlm.nih.gov/pubmed/23862079
http://dx.doi.org/10.1155/2013/706128
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author Mohanty, Neeta
Rastogi, Varun
Misra, Satya Ranjan
Mohanty, Susant
author_facet Mohanty, Neeta
Rastogi, Varun
Misra, Satya Ranjan
Mohanty, Susant
author_sort Mohanty, Neeta
collection PubMed
description Odontogenic tumors develop in the jaw bones from the odontogenic tissue-oral epithelium in tooth germ, enamel organ, dental papilla, reduced enamel epithelium, remnants of Hertwig's root sheath or dental lamina, and so forth. Hence, a bewildering variety of tumors are encountered in the maxilla and mandible. Ameloblastoma is the second most common odontogenic neoplasm after odontomes, and it has numerous clinical and histologic variants. We report a very rare histologic variant: the papilliferous keratoameloblastoma which is the fifth reported case in the English literature.
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spelling pubmed-36860742013-07-16 Papilliferous Keratoameloblastoma: An Extremely Rare Case Report Mohanty, Neeta Rastogi, Varun Misra, Satya Ranjan Mohanty, Susant Case Rep Dent Case Report Odontogenic tumors develop in the jaw bones from the odontogenic tissue-oral epithelium in tooth germ, enamel organ, dental papilla, reduced enamel epithelium, remnants of Hertwig's root sheath or dental lamina, and so forth. Hence, a bewildering variety of tumors are encountered in the maxilla and mandible. Ameloblastoma is the second most common odontogenic neoplasm after odontomes, and it has numerous clinical and histologic variants. We report a very rare histologic variant: the papilliferous keratoameloblastoma which is the fifth reported case in the English literature. Hindawi Publishing Corporation 2013 2013-06-03 /pmc/articles/PMC3686074/ /pubmed/23862079 http://dx.doi.org/10.1155/2013/706128 Text en Copyright © 2013 Neeta Mohanty 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
Mohanty, Neeta
Rastogi, Varun
Misra, Satya Ranjan
Mohanty, Susant
Papilliferous Keratoameloblastoma: An Extremely Rare Case Report
title Papilliferous Keratoameloblastoma: An Extremely Rare Case Report
title_full Papilliferous Keratoameloblastoma: An Extremely Rare Case Report
title_fullStr Papilliferous Keratoameloblastoma: An Extremely Rare Case Report
title_full_unstemmed Papilliferous Keratoameloblastoma: An Extremely Rare Case Report
title_short Papilliferous Keratoameloblastoma: An Extremely Rare Case Report
title_sort papilliferous keratoameloblastoma: an extremely rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3686074/
https://www.ncbi.nlm.nih.gov/pubmed/23862079
http://dx.doi.org/10.1155/2013/706128
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