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Myoepithelial Cell Carcinoma of the Oral Tongue: Case Report and Review of the Literature

BACKGROUND: Myoepithelial cell carcinoma is a rare malignant neoplasm of salivary gland origin that typically presents in the parotid gland and minor salivary glands. It has been described previously in head and neck sites such as buccal mucosa, alveolar ridge, and base of tongue. METHODS: A 55-year...

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Autores principales: Nicholas, Robert G, Hanson, Josh A, Meiklejohn, Duncan A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6448097/
https://www.ncbi.nlm.nih.gov/pubmed/30983863
http://dx.doi.org/10.1177/1179554919838254
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author Nicholas, Robert G
Hanson, Josh A
Meiklejohn, Duncan A
author_facet Nicholas, Robert G
Hanson, Josh A
Meiklejohn, Duncan A
author_sort Nicholas, Robert G
collection PubMed
description BACKGROUND: Myoepithelial cell carcinoma is a rare malignant neoplasm of salivary gland origin that typically presents in the parotid gland and minor salivary glands. It has been described previously in head and neck sites such as buccal mucosa, alveolar ridge, and base of tongue. METHODS: A 55-year-old man presented with 30 years of right-sided tongue pain and 10 years of gradually worsening ulceration. Physical examination demonstrated a 2.5 cm ulcerative lesion of the anterior right oral tongue. An initial biopsy was consistent with moderately to poorly differentiated squamous cell carcinoma. Imaging included a positron emission tomography (PET)/computed tomography (CT) scan that demonstrated the right tongue lesion as well as hypermetabolic right level II adenopathy. The patient underwent surgical excision of the right tongue, upper aerodigestive tract endoscopy, and a bilateral supraomohyoid neck dissection. The tongue defect was closed primarily. RESULTS: Final pathology of the surgical specimen demonstrated myoepithelial cell carcinoma. All of the margins were free of tumor and no cervical lymph nodes showed metastasis. Immunohistochemistry demonstrated myoepithelial differentiation. The tumor did not show EWSR1 gene rearrangement on genetic testing, suggesting salivary gland origin. Multidisciplinary tumor board evaluation recommended no adjuvant therapy. The patient recovered well after surgery and nearly a year later is without evidence of recurrent or residual disease. CONCLUSIONS: We present the first reported case of myoepithelial cell carcinoma with primary origin in the oral tongue and review the available literature on this unusual tumor. We discuss the clinical, pathological, and immunohistochemical features and treatment of myoepithelial cell carcinoma.
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spelling pubmed-64480972019-04-12 Myoepithelial Cell Carcinoma of the Oral Tongue: Case Report and Review of the Literature Nicholas, Robert G Hanson, Josh A Meiklejohn, Duncan A Clin Med Insights Oncol Case Report BACKGROUND: Myoepithelial cell carcinoma is a rare malignant neoplasm of salivary gland origin that typically presents in the parotid gland and minor salivary glands. It has been described previously in head and neck sites such as buccal mucosa, alveolar ridge, and base of tongue. METHODS: A 55-year-old man presented with 30 years of right-sided tongue pain and 10 years of gradually worsening ulceration. Physical examination demonstrated a 2.5 cm ulcerative lesion of the anterior right oral tongue. An initial biopsy was consistent with moderately to poorly differentiated squamous cell carcinoma. Imaging included a positron emission tomography (PET)/computed tomography (CT) scan that demonstrated the right tongue lesion as well as hypermetabolic right level II adenopathy. The patient underwent surgical excision of the right tongue, upper aerodigestive tract endoscopy, and a bilateral supraomohyoid neck dissection. The tongue defect was closed primarily. RESULTS: Final pathology of the surgical specimen demonstrated myoepithelial cell carcinoma. All of the margins were free of tumor and no cervical lymph nodes showed metastasis. Immunohistochemistry demonstrated myoepithelial differentiation. The tumor did not show EWSR1 gene rearrangement on genetic testing, suggesting salivary gland origin. Multidisciplinary tumor board evaluation recommended no adjuvant therapy. The patient recovered well after surgery and nearly a year later is without evidence of recurrent or residual disease. CONCLUSIONS: We present the first reported case of myoepithelial cell carcinoma with primary origin in the oral tongue and review the available literature on this unusual tumor. We discuss the clinical, pathological, and immunohistochemical features and treatment of myoepithelial cell carcinoma. SAGE Publications 2019-04-02 /pmc/articles/PMC6448097/ /pubmed/30983863 http://dx.doi.org/10.1177/1179554919838254 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Nicholas, Robert G
Hanson, Josh A
Meiklejohn, Duncan A
Myoepithelial Cell Carcinoma of the Oral Tongue: Case Report and Review of the Literature
title Myoepithelial Cell Carcinoma of the Oral Tongue: Case Report and Review of the Literature
title_full Myoepithelial Cell Carcinoma of the Oral Tongue: Case Report and Review of the Literature
title_fullStr Myoepithelial Cell Carcinoma of the Oral Tongue: Case Report and Review of the Literature
title_full_unstemmed Myoepithelial Cell Carcinoma of the Oral Tongue: Case Report and Review of the Literature
title_short Myoepithelial Cell Carcinoma of the Oral Tongue: Case Report and Review of the Literature
title_sort myoepithelial cell carcinoma of the oral tongue: case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6448097/
https://www.ncbi.nlm.nih.gov/pubmed/30983863
http://dx.doi.org/10.1177/1179554919838254
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