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Congenital sebaceous choristoma of the tongue: A rare case report

The most common oral choristomas are consisted of thyroid tissue and bone. The presence of sebaceous glands in the oral mucosa, especially in the buccal mucosa and labial mucosa, is often considered a normal anatomical variation since they are observed in about 80% of the population and are called e...

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Autores principales: Marques, Letícia-Côgo, Figueira, Luiza-de Moura-Carvalho, Almeida, Lilian, Rozza-de-Menezes, Rafaela-Elvira, Silva-Junior, Arley, Cunha, Karin-Soares, Conde, Danielle-Castex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094729/
https://www.ncbi.nlm.nih.gov/pubmed/35582357
http://dx.doi.org/10.4317/jced.59451
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author Marques, Letícia-Côgo
Figueira, Luiza-de Moura-Carvalho
Almeida, Lilian
Rozza-de-Menezes, Rafaela-Elvira
Silva-Junior, Arley
Cunha, Karin-Soares
Conde, Danielle-Castex
author_facet Marques, Letícia-Côgo
Figueira, Luiza-de Moura-Carvalho
Almeida, Lilian
Rozza-de-Menezes, Rafaela-Elvira
Silva-Junior, Arley
Cunha, Karin-Soares
Conde, Danielle-Castex
author_sort Marques, Letícia-Côgo
collection PubMed
description The most common oral choristomas are consisted of thyroid tissue and bone. The presence of sebaceous glands in the oral mucosa, especially in the buccal mucosa and labial mucosa, is often considered a normal anatomical variation since they are observed in about 80% of the population and are called ectopic sebaceous glands or Fordyce’s granules. However, the presence of these glands on the tongue is rare, with only 11 cases in the dorsum of the tongue reported in the English literature, and it is considered a choristoma. This paper aims to report the third case in the literature of a congenital sebaceous choristoma on the tongue. An 11-year-old white male patient presented a firm sessile papule, without color alteration, measuring 0.4 cm x 0.3 cm in diameter, in the middle third of the dorsum of the tongue with a slight increased size in the last months. Histopathological examination showed an invagination of the epithelium into the connective tissue, forming a ductal structure covered by stratified squamous epithelium. The deeper areas had normal well-differentiated sebaceous glands, with ducts connected to the central duct. Considering clinical and histopathological findings the diagnosis was sebaceous choristoma. Despite being rare, sebaceous choristomas should also be considered in the differential diagnosis of tongue abnormalities or lesions. Although the pathogenesis is not well understood, the present report, as a congenital choristoma case in the midline, reinforces the hypothesis of a disorder with embryological origin and a possible relationship with thyroglossal duct remnants. Key words:Choristoma, Oral Mucosa, Tongue.
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spelling pubmed-90947292022-05-16 Congenital sebaceous choristoma of the tongue: A rare case report Marques, Letícia-Côgo Figueira, Luiza-de Moura-Carvalho Almeida, Lilian Rozza-de-Menezes, Rafaela-Elvira Silva-Junior, Arley Cunha, Karin-Soares Conde, Danielle-Castex J Clin Exp Dent Case Report The most common oral choristomas are consisted of thyroid tissue and bone. The presence of sebaceous glands in the oral mucosa, especially in the buccal mucosa and labial mucosa, is often considered a normal anatomical variation since they are observed in about 80% of the population and are called ectopic sebaceous glands or Fordyce’s granules. However, the presence of these glands on the tongue is rare, with only 11 cases in the dorsum of the tongue reported in the English literature, and it is considered a choristoma. This paper aims to report the third case in the literature of a congenital sebaceous choristoma on the tongue. An 11-year-old white male patient presented a firm sessile papule, without color alteration, measuring 0.4 cm x 0.3 cm in diameter, in the middle third of the dorsum of the tongue with a slight increased size in the last months. Histopathological examination showed an invagination of the epithelium into the connective tissue, forming a ductal structure covered by stratified squamous epithelium. The deeper areas had normal well-differentiated sebaceous glands, with ducts connected to the central duct. Considering clinical and histopathological findings the diagnosis was sebaceous choristoma. Despite being rare, sebaceous choristomas should also be considered in the differential diagnosis of tongue abnormalities or lesions. Although the pathogenesis is not well understood, the present report, as a congenital choristoma case in the midline, reinforces the hypothesis of a disorder with embryological origin and a possible relationship with thyroglossal duct remnants. Key words:Choristoma, Oral Mucosa, Tongue. Medicina Oral S.L. 2022-05-01 /pmc/articles/PMC9094729/ /pubmed/35582357 http://dx.doi.org/10.4317/jced.59451 Text en Copyright: © 2022 Medicina Oral S.L. https://creativecommons.org/licenses/by/2.5/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
Marques, Letícia-Côgo
Figueira, Luiza-de Moura-Carvalho
Almeida, Lilian
Rozza-de-Menezes, Rafaela-Elvira
Silva-Junior, Arley
Cunha, Karin-Soares
Conde, Danielle-Castex
Congenital sebaceous choristoma of the tongue: A rare case report
title Congenital sebaceous choristoma of the tongue: A rare case report
title_full Congenital sebaceous choristoma of the tongue: A rare case report
title_fullStr Congenital sebaceous choristoma of the tongue: A rare case report
title_full_unstemmed Congenital sebaceous choristoma of the tongue: A rare case report
title_short Congenital sebaceous choristoma of the tongue: A rare case report
title_sort congenital sebaceous choristoma of the tongue: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094729/
https://www.ncbi.nlm.nih.gov/pubmed/35582357
http://dx.doi.org/10.4317/jced.59451
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