An infrequent histopathological subtype of ameloblastoma: Adenoid granular cell ameloblastoma with dentinoid

Adenoid ameloblastoma with dentinoid is a rare odontogenic tumor. Granular cell ameloblastoma also is a less common histological subtype of ameloblastoma. In this report, the patient was a 31-year-old male. The lesion was located in the right mandible and was unicystic with well-defined borders. The...

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Autores principales: Salehinejad, Jahanshah, Gholami, Mahdi, Eshghpour, Majid, Mehri, Tahere
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993068/
https://www.ncbi.nlm.nih.gov/pubmed/27605998
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author Salehinejad, Jahanshah
Gholami, Mahdi
Eshghpour, Majid
Mehri, Tahere
author_facet Salehinejad, Jahanshah
Gholami, Mahdi
Eshghpour, Majid
Mehri, Tahere
author_sort Salehinejad, Jahanshah
collection PubMed
description Adenoid ameloblastoma with dentinoid is a rare odontogenic tumor. Granular cell ameloblastoma also is a less common histological subtype of ameloblastoma. In this report, the patient was a 31-year-old male. The lesion was located in the right mandible and was unicystic with well-defined borders. The tumor tissue was showing a combination of follicular, plexiform, and desmoplastic patterns of ameloblastoma with wide areas of granular cells, fibrous stroma, glandular pattern, and dentinoid calcified. Very few cases of distinct forms of ameloblastoma that show the formation of dentinoid has been reported. However, there are no cases of adenoid granular cell ameloblastoma with dentinoid reported.
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spelling pubmed-49930682016-09-07 An infrequent histopathological subtype of ameloblastoma: Adenoid granular cell ameloblastoma with dentinoid Salehinejad, Jahanshah Gholami, Mahdi Eshghpour, Majid Mehri, Tahere Dent Res J (Isfahan) Case Report Adenoid ameloblastoma with dentinoid is a rare odontogenic tumor. Granular cell ameloblastoma also is a less common histological subtype of ameloblastoma. In this report, the patient was a 31-year-old male. The lesion was located in the right mandible and was unicystic with well-defined borders. The tumor tissue was showing a combination of follicular, plexiform, and desmoplastic patterns of ameloblastoma with wide areas of granular cells, fibrous stroma, glandular pattern, and dentinoid calcified. Very few cases of distinct forms of ameloblastoma that show the formation of dentinoid has been reported. However, there are no cases of adenoid granular cell ameloblastoma with dentinoid reported. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4993068/ /pubmed/27605998 Text en Copyright: © Dental Research Journal 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
Salehinejad, Jahanshah
Gholami, Mahdi
Eshghpour, Majid
Mehri, Tahere
An infrequent histopathological subtype of ameloblastoma: Adenoid granular cell ameloblastoma with dentinoid
title An infrequent histopathological subtype of ameloblastoma: Adenoid granular cell ameloblastoma with dentinoid
title_full An infrequent histopathological subtype of ameloblastoma: Adenoid granular cell ameloblastoma with dentinoid
title_fullStr An infrequent histopathological subtype of ameloblastoma: Adenoid granular cell ameloblastoma with dentinoid
title_full_unstemmed An infrequent histopathological subtype of ameloblastoma: Adenoid granular cell ameloblastoma with dentinoid
title_short An infrequent histopathological subtype of ameloblastoma: Adenoid granular cell ameloblastoma with dentinoid
title_sort infrequent histopathological subtype of ameloblastoma: adenoid granular cell ameloblastoma with dentinoid
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993068/
https://www.ncbi.nlm.nih.gov/pubmed/27605998
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