Clear cell myoepithelial carcinoma ex pleomorphic adenoma of parotid gland: Case report and review of literature

Myoepithelial carcinoma (MC), also known as malignant myoepithelioma, shows an infiltrative and destructive growth [1]. Myoepithelial neoplasms account for about 1.5% of all salivary tumors, and MC is even more rare, representing about 10% of myoepitheliomas [1–3] with a reported incidence of 0.2% o...

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Main Authors: Antonio Romano, Giovanni Dell'Aversana Orabona, Antonio Pansini, Giovanni Salzano, Immacolata Cozzolino, Miriam Cieri, Giorgio Iaconetta, Luigi Califano
Format: Article
Language:English
Published: Elsevier 2018-03-01
Series:Oral and Maxillofacial Surgery Cases
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2214541917300329
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spelling doaj-1f67a5e9f5d74b3299a7aa32ace483722020-11-24T23:17:55ZengElsevierOral and Maxillofacial Surgery Cases2214-54192018-03-0141121610.1016/j.omsc.2017.12.002Clear cell myoepithelial carcinoma ex pleomorphic adenoma of parotid gland: Case report and review of literatureAntonio Romano0Giovanni Dell'Aversana Orabona1Antonio Pansini2Giovanni Salzano3Immacolata Cozzolino4Miriam Cieri5Giorgio Iaconetta6Luigi Califano7Department of Maxillofacial Surgery, University of Naples Federico II, Naples, ItalyDepartment of Maxillofacial Surgery, University of Naples Federico II, Naples, ItalyDepartment of Maxillofacial Surgery, University of Naples Federico II, Naples, ItalyDepartment of Maxillofacial Surgery, University of Naples Federico II, Naples, ItalyDepartment of Advanced Biomedical Sciences, University of Naples Federico II, Naples, ItalyDepartment of Advanced Biomedical Sciences, University of Naples Federico II, Naples, ItalyDepartment of Neurosurgery, University of Salerno, Salerno, ItalyDepartment of Maxillofacial Surgery, University of Naples Federico II, Naples, ItalyMyoepithelial carcinoma (MC), also known as malignant myoepithelioma, shows an infiltrative and destructive growth [1]. Myoepithelial neoplasms account for about 1.5% of all salivary tumors, and MC is even more rare, representing about 10% of myoepitheliomas [1–3] with a reported incidence of 0.2% of all salivary gland tumors. In this case, the cytological diagnosis (pleomorphic adenoma) and negative lymph nodes, addressed the surgeon for a parotidectomy, following guidelines and literature [27]. The best treatment for huge, relapsing tumors, notwithstanding cytological diagnosis, is not only parotidectomy, as lymphadenectomy should be performed too, given myoepithelial carcinoma's high-grade potential and unpredictable biologic behavior. Careful patient follow-up and staging, is therefore essential for better characterization and understanding of this tumor's behavior in the future. We also considered a more conservative treatment following guidelines, as this case was lacking metastases and lymphatic involvement, considering that application of guidelines, surgical and clinical expertise and appropriate technology can contain potential medicolegal implications [28].http://www.sciencedirect.com/science/article/pii/S2214541917300329Myoepithelial carcinomaNeoplasmsParotid glandSalivary gland
collection DOAJ
language English
format Article
sources DOAJ
author Antonio Romano
Giovanni Dell'Aversana Orabona
Antonio Pansini
Giovanni Salzano
Immacolata Cozzolino
Miriam Cieri
Giorgio Iaconetta
Luigi Califano
spellingShingle Antonio Romano
Giovanni Dell'Aversana Orabona
Antonio Pansini
Giovanni Salzano
Immacolata Cozzolino
Miriam Cieri
Giorgio Iaconetta
Luigi Califano
Clear cell myoepithelial carcinoma ex pleomorphic adenoma of parotid gland: Case report and review of literature
Oral and Maxillofacial Surgery Cases
Myoepithelial carcinoma
Neoplasms
Parotid gland
Salivary gland
author_facet Antonio Romano
Giovanni Dell'Aversana Orabona
Antonio Pansini
Giovanni Salzano
Immacolata Cozzolino
Miriam Cieri
Giorgio Iaconetta
Luigi Califano
author_sort Antonio Romano
title Clear cell myoepithelial carcinoma ex pleomorphic adenoma of parotid gland: Case report and review of literature
title_short Clear cell myoepithelial carcinoma ex pleomorphic adenoma of parotid gland: Case report and review of literature
title_full Clear cell myoepithelial carcinoma ex pleomorphic adenoma of parotid gland: Case report and review of literature
title_fullStr Clear cell myoepithelial carcinoma ex pleomorphic adenoma of parotid gland: Case report and review of literature
title_full_unstemmed Clear cell myoepithelial carcinoma ex pleomorphic adenoma of parotid gland: Case report and review of literature
title_sort clear cell myoepithelial carcinoma ex pleomorphic adenoma of parotid gland: case report and review of literature
publisher Elsevier
series Oral and Maxillofacial Surgery Cases
issn 2214-5419
publishDate 2018-03-01
description Myoepithelial carcinoma (MC), also known as malignant myoepithelioma, shows an infiltrative and destructive growth [1]. Myoepithelial neoplasms account for about 1.5% of all salivary tumors, and MC is even more rare, representing about 10% of myoepitheliomas [1–3] with a reported incidence of 0.2% of all salivary gland tumors. In this case, the cytological diagnosis (pleomorphic adenoma) and negative lymph nodes, addressed the surgeon for a parotidectomy, following guidelines and literature [27]. The best treatment for huge, relapsing tumors, notwithstanding cytological diagnosis, is not only parotidectomy, as lymphadenectomy should be performed too, given myoepithelial carcinoma's high-grade potential and unpredictable biologic behavior. Careful patient follow-up and staging, is therefore essential for better characterization and understanding of this tumor's behavior in the future. We also considered a more conservative treatment following guidelines, as this case was lacking metastases and lymphatic involvement, considering that application of guidelines, surgical and clinical expertise and appropriate technology can contain potential medicolegal implications [28].
topic Myoepithelial carcinoma
Neoplasms
Parotid gland
Salivary gland
url http://www.sciencedirect.com/science/article/pii/S2214541917300329
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