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Keratoameloblastoma of the mandible

Keratoameloblastoma is a very rare ameloblastoma variant defined by extensive squamous metaplasia and keratinization. There are 13 previously reported cases in the literature, with a male predilection of 3:1. A 38-year-old male presented with a painless mandibular swelling which had been progressive...

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Detalles Bibliográficos
Autores principales: Adeyemi, BF, Adisa, AO, Fasola, AO, Akang, EE
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125065/
https://www.ncbi.nlm.nih.gov/pubmed/21731268
http://dx.doi.org/10.4103/0973-029X.72507
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author Adeyemi, BF
Adisa, AO
Fasola, AO
Akang, EE
author_facet Adeyemi, BF
Adisa, AO
Fasola, AO
Akang, EE
author_sort Adeyemi, BF
collection PubMed
description Keratoameloblastoma is a very rare ameloblastoma variant defined by extensive squamous metaplasia and keratinization. There are 13 previously reported cases in the literature, with a male predilection of 3:1. A 38-year-old male presented with a painless mandibular swelling which had been progressively increasing in size for 18 months. The incisional biopsy was misdiagnosed as basaloid squamous carcinoma. Owing to financial constraints, the patient had mandibular resection a decade after first noticing the growth, during which the clinical course was essentially benign, thus casting doubt on the initial diagnosis. The final histological diagnosis for both the incisional and resection biopsy specimens was keratoameloblastoma.
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spelling pubmed-31250652011-07-01 Keratoameloblastoma of the mandible Adeyemi, BF Adisa, AO Fasola, AO Akang, EE J Oral Maxillofac Pathol Case Report Keratoameloblastoma is a very rare ameloblastoma variant defined by extensive squamous metaplasia and keratinization. There are 13 previously reported cases in the literature, with a male predilection of 3:1. A 38-year-old male presented with a painless mandibular swelling which had been progressively increasing in size for 18 months. The incisional biopsy was misdiagnosed as basaloid squamous carcinoma. Owing to financial constraints, the patient had mandibular resection a decade after first noticing the growth, during which the clinical course was essentially benign, thus casting doubt on the initial diagnosis. The final histological diagnosis for both the incisional and resection biopsy specimens was keratoameloblastoma. Medknow Publications 2010 /pmc/articles/PMC3125065/ /pubmed/21731268 http://dx.doi.org/10.4103/0973-029X.72507 Text en © Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of 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
Adeyemi, BF
Adisa, AO
Fasola, AO
Akang, EE
Keratoameloblastoma of the mandible
title Keratoameloblastoma of the mandible
title_full Keratoameloblastoma of the mandible
title_fullStr Keratoameloblastoma of the mandible
title_full_unstemmed Keratoameloblastoma of the mandible
title_short Keratoameloblastoma of the mandible
title_sort keratoameloblastoma of the mandible
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125065/
https://www.ncbi.nlm.nih.gov/pubmed/21731268
http://dx.doi.org/10.4103/0973-029X.72507
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