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Sialolipoma of parotid gland in a 1-year-old male child: A case report and review of literature

Sialolipoma is a recently described rare histological variant of lipoma, characterized by well-demarcated proliferation of mature adipocytes with secondary entrapment of salivary gland elements. Less than forty cases of sialolipoma have been reported in English literature. This tumor has been report...

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Detalles Bibliográficos
Autores principales: Arakeri, Surekha Ulhas, Banga, Shilpi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824519/
https://www.ncbi.nlm.nih.gov/pubmed/29491607
http://dx.doi.org/10.4103/jomfp.JOMFP_38_15
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author Arakeri, Surekha Ulhas
Banga, Shilpi
author_facet Arakeri, Surekha Ulhas
Banga, Shilpi
author_sort Arakeri, Surekha Ulhas
collection PubMed
description Sialolipoma is a recently described rare histological variant of lipoma, characterized by well-demarcated proliferation of mature adipocytes with secondary entrapment of salivary gland elements. Less than forty cases of sialolipoma have been reported in English literature. This tumor has been reported both in major and minor salivary glands, with the parotid gland being the most common site. Age incidence in this tumor varies from 0 month to 84 years. However, the occurrence of this tumor in an infant is very rare. In the published literature, the size of this tumor varied from 1 to 7 cm. In the present case, the tumor size was >7 cm. To the best of our knowledge, congenital sialolipoma >7 cm has been rarely reported earlier. Hence, this case is presented because of its rarity and unusual gross appearance.
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spelling pubmed-58245192018-02-28 Sialolipoma of parotid gland in a 1-year-old male child: A case report and review of literature Arakeri, Surekha Ulhas Banga, Shilpi J Oral Maxillofac Pathol Case Report Sialolipoma is a recently described rare histological variant of lipoma, characterized by well-demarcated proliferation of mature adipocytes with secondary entrapment of salivary gland elements. Less than forty cases of sialolipoma have been reported in English literature. This tumor has been reported both in major and minor salivary glands, with the parotid gland being the most common site. Age incidence in this tumor varies from 0 month to 84 years. However, the occurrence of this tumor in an infant is very rare. In the published literature, the size of this tumor varied from 1 to 7 cm. In the present case, the tumor size was >7 cm. To the best of our knowledge, congenital sialolipoma >7 cm has been rarely reported earlier. Hence, this case is presented because of its rarity and unusual gross appearance. Medknow Publications & Media Pvt Ltd 2018-01 /pmc/articles/PMC5824519/ /pubmed/29491607 http://dx.doi.org/10.4103/jomfp.JOMFP_38_15 Text en Copyright: © 2018 Journal of Oral and Maxillofacial Pathology 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
Arakeri, Surekha Ulhas
Banga, Shilpi
Sialolipoma of parotid gland in a 1-year-old male child: A case report and review of literature
title Sialolipoma of parotid gland in a 1-year-old male child: A case report and review of literature
title_full Sialolipoma of parotid gland in a 1-year-old male child: A case report and review of literature
title_fullStr Sialolipoma of parotid gland in a 1-year-old male child: A case report and review of literature
title_full_unstemmed Sialolipoma of parotid gland in a 1-year-old male child: A case report and review of literature
title_short Sialolipoma of parotid gland in a 1-year-old male child: A case report and review of literature
title_sort sialolipoma of parotid gland in a 1-year-old male child: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824519/
https://www.ncbi.nlm.nih.gov/pubmed/29491607
http://dx.doi.org/10.4103/jomfp.JOMFP_38_15
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