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An unusual presentation of an odontogenic tumor: A diagnostic quandary

Squamous odontogenic tumor (SOT) is a rare benign neoplasm and may be located to multiple sites in the oral cavity mouth. As per the literature, there have been <50 reported cases. The tumor is often asymptomatic, although it can present with symptoms of pain and tooth mobility. Peripheral odonto...

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Autores principales: Thomas, Priya, Sebastian, Aneesh, Krishnapillai, Rekha, Chandran, Sapna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123245/
https://www.ncbi.nlm.nih.gov/pubmed/34083981
http://dx.doi.org/10.4103/jomfp.JOMFP_147_20
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author Thomas, Priya
Sebastian, Aneesh
Krishnapillai, Rekha
Chandran, Sapna
author_facet Thomas, Priya
Sebastian, Aneesh
Krishnapillai, Rekha
Chandran, Sapna
author_sort Thomas, Priya
collection PubMed
description Squamous odontogenic tumor (SOT) is a rare benign neoplasm and may be located to multiple sites in the oral cavity mouth. As per the literature, there have been <50 reported cases. The tumor is often asymptomatic, although it can present with symptoms of pain and tooth mobility. Peripheral odontogenic tumor is a rare entity derived from either epithelial or mesenchymal portions of the tooth-forming apparatus. Lesions are common to gingiva and alveolar mucosa. Peripheral granular cell ameloblastoma (GCA) is considered to be even rarer. The purpose of the study is to report a case of SOT with a synchronous association with peripheral GCA of cystic nature in the mandible. The occurrence of SOT with ameloblastoma has not been reported as per the literature search.
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spelling pubmed-81232452021-06-02 An unusual presentation of an odontogenic tumor: A diagnostic quandary Thomas, Priya Sebastian, Aneesh Krishnapillai, Rekha Chandran, Sapna J Oral Maxillofac Pathol Case Report Squamous odontogenic tumor (SOT) is a rare benign neoplasm and may be located to multiple sites in the oral cavity mouth. As per the literature, there have been <50 reported cases. The tumor is often asymptomatic, although it can present with symptoms of pain and tooth mobility. Peripheral odontogenic tumor is a rare entity derived from either epithelial or mesenchymal portions of the tooth-forming apparatus. Lesions are common to gingiva and alveolar mucosa. Peripheral granular cell ameloblastoma (GCA) is considered to be even rarer. The purpose of the study is to report a case of SOT with a synchronous association with peripheral GCA of cystic nature in the mandible. The occurrence of SOT with ameloblastoma has not been reported as per the literature search. Wolters Kluwer - Medknow 2021-03 2021-03-19 /pmc/articles/PMC8123245/ /pubmed/34083981 http://dx.doi.org/10.4103/jomfp.JOMFP_147_20 Text en Copyright: © 2021 Journal of Oral and Maxillofacial Pathology https://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
Thomas, Priya
Sebastian, Aneesh
Krishnapillai, Rekha
Chandran, Sapna
An unusual presentation of an odontogenic tumor: A diagnostic quandary
title An unusual presentation of an odontogenic tumor: A diagnostic quandary
title_full An unusual presentation of an odontogenic tumor: A diagnostic quandary
title_fullStr An unusual presentation of an odontogenic tumor: A diagnostic quandary
title_full_unstemmed An unusual presentation of an odontogenic tumor: A diagnostic quandary
title_short An unusual presentation of an odontogenic tumor: A diagnostic quandary
title_sort unusual presentation of an odontogenic tumor: a diagnostic quandary
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123245/
https://www.ncbi.nlm.nih.gov/pubmed/34083981
http://dx.doi.org/10.4103/jomfp.JOMFP_147_20
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