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Papillary cystic variant of acinic cell carcinoma presenting as parotid tail tumor

Acinic cell carcinoma (ACC) is an uncommon low-grade tumor of the salivary glands that constitutes 2.5–4% of parotid gland tumors. Papillary cystic variant (PCV) of ACC is even rarer and can be diagnosed on histopathological examination only. It is important to diagnose this variant as it carries a...

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Autores principales: Khan, Sabina, Pujani, Mukta, Hassan, Mohd Jaseem, Jetley, Sujata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456890/
https://www.ncbi.nlm.nih.gov/pubmed/26097824
http://dx.doi.org/10.4103/2229-516X.157171
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author Khan, Sabina
Pujani, Mukta
Hassan, Mohd Jaseem
Jetley, Sujata
author_facet Khan, Sabina
Pujani, Mukta
Hassan, Mohd Jaseem
Jetley, Sujata
author_sort Khan, Sabina
collection PubMed
description Acinic cell carcinoma (ACC) is an uncommon low-grade tumor of the salivary glands that constitutes 2.5–4% of parotid gland tumors. Papillary cystic variant (PCV) of ACC is even rarer and can be diagnosed on histopathological examination only. It is important to diagnose this variant as it carries a poor prognosis when compared with other variants of ACC and is known to be universally fatal in 10 years. The present case describes ACC-PCV in a 20-year-old male, which presented as a slow growing parotid tail tumor and was misdiagnosed as a benign lesion both cytologically and radiologically. This case emphasizes the importance of histopathological examination in parotid masses as well as the need to consider malignant lesion in the differential diagnosis of a parotid tail tumor.
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spelling pubmed-44568902015-06-19 Papillary cystic variant of acinic cell carcinoma presenting as parotid tail tumor Khan, Sabina Pujani, Mukta Hassan, Mohd Jaseem Jetley, Sujata Int J Appl Basic Med Res Case Report Acinic cell carcinoma (ACC) is an uncommon low-grade tumor of the salivary glands that constitutes 2.5–4% of parotid gland tumors. Papillary cystic variant (PCV) of ACC is even rarer and can be diagnosed on histopathological examination only. It is important to diagnose this variant as it carries a poor prognosis when compared with other variants of ACC and is known to be universally fatal in 10 years. The present case describes ACC-PCV in a 20-year-old male, which presented as a slow growing parotid tail tumor and was misdiagnosed as a benign lesion both cytologically and radiologically. This case emphasizes the importance of histopathological examination in parotid masses as well as the need to consider malignant lesion in the differential diagnosis of a parotid tail tumor. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4456890/ /pubmed/26097824 http://dx.doi.org/10.4103/2229-516X.157171 Text en Copyright: © International Journal of Applied and Basic Medical Research 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 Report
Khan, Sabina
Pujani, Mukta
Hassan, Mohd Jaseem
Jetley, Sujata
Papillary cystic variant of acinic cell carcinoma presenting as parotid tail tumor
title Papillary cystic variant of acinic cell carcinoma presenting as parotid tail tumor
title_full Papillary cystic variant of acinic cell carcinoma presenting as parotid tail tumor
title_fullStr Papillary cystic variant of acinic cell carcinoma presenting as parotid tail tumor
title_full_unstemmed Papillary cystic variant of acinic cell carcinoma presenting as parotid tail tumor
title_short Papillary cystic variant of acinic cell carcinoma presenting as parotid tail tumor
title_sort papillary cystic variant of acinic cell carcinoma presenting as parotid tail tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456890/
https://www.ncbi.nlm.nih.gov/pubmed/26097824
http://dx.doi.org/10.4103/2229-516X.157171
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