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Granular Cell Odontogenic Tumor, an Extremely Rare Case Report
The granular cell odontogenic tumor is an extremely rare odontogenic neoplasm which about 38 cases has been reported with sufficient documentation in the literature. It has a prominent predilection to occur in the posterior of mandible of middle-aged women. Here, we report a case of mandibular granu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Journal of Dentistry Shiraz University of Medical Sciences
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732182/ https://www.ncbi.nlm.nih.gov/pubmed/31579699 http://dx.doi.org/10.30476/DENTJODS.2019.82390.1018 |
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author | Atarbashi-Moghadam, Saede Saebnoori, Homeira Shamloo, Nafiseh Dehghanpour Barouj, Mehrdad Saedi, Sara |
author_facet | Atarbashi-Moghadam, Saede Saebnoori, Homeira Shamloo, Nafiseh Dehghanpour Barouj, Mehrdad Saedi, Sara |
author_sort | Atarbashi-Moghadam, Saede |
collection | PubMed |
description | The granular cell odontogenic tumor is an extremely rare odontogenic neoplasm which about 38 cases has been reported with sufficient documentation in the literature. It has a prominent predilection to occur in the posterior of mandible of middle-aged women. Here, we report a case of mandibular granular cell odontogenic tumor in a 57-year-old female with chief complaint of swelling and tooth mobility. As rarity of these lesions, their clinical behavior and prognosis are not clear; hence, reporting more such cases may be beneficial to correct diagnosis and prevent unnecessary treatment. |
format | Online Article Text |
id | pubmed-6732182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Journal of Dentistry Shiraz University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-67321822019-10-02 Granular Cell Odontogenic Tumor, an Extremely Rare Case Report Atarbashi-Moghadam, Saede Saebnoori, Homeira Shamloo, Nafiseh Dehghanpour Barouj, Mehrdad Saedi, Sara J Dent (Shiraz) Case Reports The granular cell odontogenic tumor is an extremely rare odontogenic neoplasm which about 38 cases has been reported with sufficient documentation in the literature. It has a prominent predilection to occur in the posterior of mandible of middle-aged women. Here, we report a case of mandibular granular cell odontogenic tumor in a 57-year-old female with chief complaint of swelling and tooth mobility. As rarity of these lesions, their clinical behavior and prognosis are not clear; hence, reporting more such cases may be beneficial to correct diagnosis and prevent unnecessary treatment. Journal of Dentistry Shiraz University of Medical Sciences 2019-09 /pmc/articles/PMC6732182/ /pubmed/31579699 http://dx.doi.org/10.30476/DENTJODS.2019.82390.1018 Text en Copyright: © Journal of Dentistry Shiraz University of Medical Sciences 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Atarbashi-Moghadam, Saede Saebnoori, Homeira Shamloo, Nafiseh Dehghanpour Barouj, Mehrdad Saedi, Sara Granular Cell Odontogenic Tumor, an Extremely Rare Case Report |
title | Granular Cell Odontogenic Tumor, an Extremely Rare Case Report
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title_full | Granular Cell Odontogenic Tumor, an Extremely Rare Case Report
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title_fullStr | Granular Cell Odontogenic Tumor, an Extremely Rare Case Report
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title_full_unstemmed | Granular Cell Odontogenic Tumor, an Extremely Rare Case Report
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title_short | Granular Cell Odontogenic Tumor, an Extremely Rare Case Report
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title_sort | granular cell odontogenic tumor, an extremely rare case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732182/ https://www.ncbi.nlm.nih.gov/pubmed/31579699 http://dx.doi.org/10.30476/DENTJODS.2019.82390.1018 |
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