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Ectomesenchymal chondromyxoid tumor: Review of literature and a report of a rare case

Ectomesenchymal chondromyxoid tumor (ECMT) is a rare benign intraoral tumor. Clinically, it presents as a slow growing, painless, firm, submucosal sweling exclusively occurring on the anterior dorsum of the tongue. Till date only 40 cases have been reported in literature. Histopathologically the tum...

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Detalles Bibliográficos
Autores principales: Leeky, Mohanty, Narayan, TV, Shenoy, Sadhana, Jamadar, Saleha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125662/
https://www.ncbi.nlm.nih.gov/pubmed/21731283
http://dx.doi.org/10.4103/0973-029X.80021
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author Leeky, Mohanty
Narayan, TV
Shenoy, Sadhana
Jamadar, Saleha
author_facet Leeky, Mohanty
Narayan, TV
Shenoy, Sadhana
Jamadar, Saleha
author_sort Leeky, Mohanty
collection PubMed
description Ectomesenchymal chondromyxoid tumor (ECMT) is a rare benign intraoral tumor. Clinically, it presents as a slow growing, painless, firm, submucosal sweling exclusively occurring on the anterior dorsum of the tongue. Till date only 40 cases have been reported in literature. Histopathologically the tumor is characterized by a well circumscribed, lobular proliferation of round, polygonal, ovoid or fusiform cells in a net-like pattern in a myxoid to chondromyxoid background. Here, we present a rare case of ECMT occurring in a 7-year-old boy and throw some light on this distinct entity.
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spelling pubmed-31256622011-07-01 Ectomesenchymal chondromyxoid tumor: Review of literature and a report of a rare case Leeky, Mohanty Narayan, TV Shenoy, Sadhana Jamadar, Saleha J Oral Maxillofac Pathol Case Report Ectomesenchymal chondromyxoid tumor (ECMT) is a rare benign intraoral tumor. Clinically, it presents as a slow growing, painless, firm, submucosal sweling exclusively occurring on the anterior dorsum of the tongue. Till date only 40 cases have been reported in literature. Histopathologically the tumor is characterized by a well circumscribed, lobular proliferation of round, polygonal, ovoid or fusiform cells in a net-like pattern in a myxoid to chondromyxoid background. Here, we present a rare case of ECMT occurring in a 7-year-old boy and throw some light on this distinct entity. Medknow Publications 2011 /pmc/articles/PMC3125662/ /pubmed/21731283 http://dx.doi.org/10.4103/0973-029X.80021 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
Leeky, Mohanty
Narayan, TV
Shenoy, Sadhana
Jamadar, Saleha
Ectomesenchymal chondromyxoid tumor: Review of literature and a report of a rare case
title Ectomesenchymal chondromyxoid tumor: Review of literature and a report of a rare case
title_full Ectomesenchymal chondromyxoid tumor: Review of literature and a report of a rare case
title_fullStr Ectomesenchymal chondromyxoid tumor: Review of literature and a report of a rare case
title_full_unstemmed Ectomesenchymal chondromyxoid tumor: Review of literature and a report of a rare case
title_short Ectomesenchymal chondromyxoid tumor: Review of literature and a report of a rare case
title_sort ectomesenchymal chondromyxoid tumor: review of literature and a report of a rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125662/
https://www.ncbi.nlm.nih.gov/pubmed/21731283
http://dx.doi.org/10.4103/0973-029X.80021
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