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Salivary duct carcinoma of accessory parotid

Accessory parotid gland (APG) is seen in around 21%–56% of individuals. Tumors of accessory parotid are uncommon with an incidence rate of 1%–8% of all parotid tumors. Ductal carcinoma of APG is rare, so no reported incidence was seen in the literature. However, salivary gland ductal carcinoma is re...

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Autores principales: Al-Hashim, Mohammed A., Al-Jazan, Nasser A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596634/
https://www.ncbi.nlm.nih.gov/pubmed/28932166
http://dx.doi.org/10.4103/jfcm.JFCM_141_16
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author Al-Hashim, Mohammed A.
Al-Jazan, Nasser A.
author_facet Al-Hashim, Mohammed A.
Al-Jazan, Nasser A.
author_sort Al-Hashim, Mohammed A.
collection PubMed
description Accessory parotid gland (APG) is seen in around 21%–56% of individuals. Tumors of accessory parotid are uncommon with an incidence rate of 1%–8% of all parotid tumors. Ductal carcinoma of APG is rare, so no reported incidence was seen in the literature. However, salivary gland ductal carcinoma is reported to be 1% of all salivary gland neoplasms. We report here a case of salivary duct carcinoma of APG. Clinical presentation, investigation, and management are discussed. A 69-year-old female presented with a history of the left cheek progressive swelling of 6 years' duration. Computed tomography and magnetic resonance imaging showed heterogeneous lobulated ill-defined mass over the left masseter. Fine needle aspiration was inconclusive. Excision of the mass showed salivary duct carcinoma. Ductal carcinoma of APG is an aggressive tumor which needs to be managed aggressively. Standard parotidectomy incision approach seems to be a safe and efficient way of management.
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spelling pubmed-55966342017-09-20 Salivary duct carcinoma of accessory parotid Al-Hashim, Mohammed A. Al-Jazan, Nasser A. J Family Community Med Case Report Accessory parotid gland (APG) is seen in around 21%–56% of individuals. Tumors of accessory parotid are uncommon with an incidence rate of 1%–8% of all parotid tumors. Ductal carcinoma of APG is rare, so no reported incidence was seen in the literature. However, salivary gland ductal carcinoma is reported to be 1% of all salivary gland neoplasms. We report here a case of salivary duct carcinoma of APG. Clinical presentation, investigation, and management are discussed. A 69-year-old female presented with a history of the left cheek progressive swelling of 6 years' duration. Computed tomography and magnetic resonance imaging showed heterogeneous lobulated ill-defined mass over the left masseter. Fine needle aspiration was inconclusive. Excision of the mass showed salivary duct carcinoma. Ductal carcinoma of APG is an aggressive tumor which needs to be managed aggressively. Standard parotidectomy incision approach seems to be a safe and efficient way of management. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5596634/ /pubmed/28932166 http://dx.doi.org/10.4103/jfcm.JFCM_141_16 Text en Copyright: © 2017 Journal of Family and Community Medicine 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
Al-Hashim, Mohammed A.
Al-Jazan, Nasser A.
Salivary duct carcinoma of accessory parotid
title Salivary duct carcinoma of accessory parotid
title_full Salivary duct carcinoma of accessory parotid
title_fullStr Salivary duct carcinoma of accessory parotid
title_full_unstemmed Salivary duct carcinoma of accessory parotid
title_short Salivary duct carcinoma of accessory parotid
title_sort salivary duct carcinoma of accessory parotid
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596634/
https://www.ncbi.nlm.nih.gov/pubmed/28932166
http://dx.doi.org/10.4103/jfcm.JFCM_141_16
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