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Rare Development of Primary Parotid Gland Epithelial-Myoepithelial Carcinoma in a Child

Salivary gland tumors are uncommon in children. They consist of variable histopathological subtypes of benign and malignant tumors. EMC is a discrete entity among the WHO classification of salivary gland tumors since 1991. EMC is considered a low-grade malignant salivary gland tumor arising from int...

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Autores principales: Saleh, Daniyah, Al Ghamdi, Doaa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345586/
https://www.ncbi.nlm.nih.gov/pubmed/32665872
http://dx.doi.org/10.1155/2020/5837659
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author Saleh, Daniyah
Al Ghamdi, Doaa
author_facet Saleh, Daniyah
Al Ghamdi, Doaa
author_sort Saleh, Daniyah
collection PubMed
description Salivary gland tumors are uncommon in children. They consist of variable histopathological subtypes of benign and malignant tumors. EMC is a discrete entity among the WHO classification of salivary gland tumors since 1991. EMC is considered a low-grade malignant salivary gland tumor arising from intercalated ducts. Typically, it affects an adult female individual. Surgical resection with a negative margin is the mainstay treatment option. EMC has a potential for metastasis with a high rate of recurrence. Based on the available English literature, two cases of EMC diagnosed in a pediatric age group have been reported. Therefore, we describe the third EMC that developed in the left parotid gland of a young child. The diagnosis of EMC was established through histopathological examination of the total parotidectomy specimen and neck lymph node dissection, together with ancillary studies. Later, the patient suffered from cervical lymph node enlargement due to metastasis in which FNAB was taken. Metastasis from the known EMC was suspected with cytomorphological features in smears and cell block. Immunohistochemistry markers for the biphasic components were supportive of EMC. Due to advanced disease, the patient necessitated a concomitant treatment of radiochemotherapy. Besides, there was radiological evidence of bilateral multiple lung metastatic nodules. However, a biopsy was not sent for pathological confirmation.
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spelling pubmed-73455862020-07-13 Rare Development of Primary Parotid Gland Epithelial-Myoepithelial Carcinoma in a Child Saleh, Daniyah Al Ghamdi, Doaa Case Rep Pathol Case Report Salivary gland tumors are uncommon in children. They consist of variable histopathological subtypes of benign and malignant tumors. EMC is a discrete entity among the WHO classification of salivary gland tumors since 1991. EMC is considered a low-grade malignant salivary gland tumor arising from intercalated ducts. Typically, it affects an adult female individual. Surgical resection with a negative margin is the mainstay treatment option. EMC has a potential for metastasis with a high rate of recurrence. Based on the available English literature, two cases of EMC diagnosed in a pediatric age group have been reported. Therefore, we describe the third EMC that developed in the left parotid gland of a young child. The diagnosis of EMC was established through histopathological examination of the total parotidectomy specimen and neck lymph node dissection, together with ancillary studies. Later, the patient suffered from cervical lymph node enlargement due to metastasis in which FNAB was taken. Metastasis from the known EMC was suspected with cytomorphological features in smears and cell block. Immunohistochemistry markers for the biphasic components were supportive of EMC. Due to advanced disease, the patient necessitated a concomitant treatment of radiochemotherapy. Besides, there was radiological evidence of bilateral multiple lung metastatic nodules. However, a biopsy was not sent for pathological confirmation. Hindawi 2020-06-30 /pmc/articles/PMC7345586/ /pubmed/32665872 http://dx.doi.org/10.1155/2020/5837659 Text en Copyright © 2020 Daniyah Saleh and Doaa Al Ghamdi. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under 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
Saleh, Daniyah
Al Ghamdi, Doaa
Rare Development of Primary Parotid Gland Epithelial-Myoepithelial Carcinoma in a Child
title Rare Development of Primary Parotid Gland Epithelial-Myoepithelial Carcinoma in a Child
title_full Rare Development of Primary Parotid Gland Epithelial-Myoepithelial Carcinoma in a Child
title_fullStr Rare Development of Primary Parotid Gland Epithelial-Myoepithelial Carcinoma in a Child
title_full_unstemmed Rare Development of Primary Parotid Gland Epithelial-Myoepithelial Carcinoma in a Child
title_short Rare Development of Primary Parotid Gland Epithelial-Myoepithelial Carcinoma in a Child
title_sort rare development of primary parotid gland epithelial-myoepithelial carcinoma in a child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345586/
https://www.ncbi.nlm.nih.gov/pubmed/32665872
http://dx.doi.org/10.1155/2020/5837659
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