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De novo myoepithelial carcinoma with multiple metastases arising from a submandibular salivary gland: A case report

Salivary gland carcinomas are rare tumors, representing ~0.5% of all malignancies. Myoepithelioma is also uncommon, representing ~1% of all salivary gland tumors. Myoepithelial carcinoma (MC) is even rarer, representing 0.2 to 0.6% of all salivary gland tumors. We herein report a case of MC with mul...

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Detalles Bibliográficos
Autores principales: Panelli Santos, Karina Cecília Panelli, Matsuzaki, Hidenobu, Unetsubo, Teruhisa, Tsuyoshi, Shimo, Nagatsuka, Hitoshi, Asaumi, Jun-Ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403181/
https://www.ncbi.nlm.nih.gov/pubmed/28454450
http://dx.doi.org/10.3892/ol.2017.5783
Descripción
Sumario:Salivary gland carcinomas are rare tumors, representing ~0.5% of all malignancies. Myoepithelioma is also uncommon, representing ~1% of all salivary gland tumors. Myoepithelial carcinoma (MC) is even rarer, representing 0.2 to 0.6% of all salivary gland tumors. We herein report a case of MC with multiple metastases arising from a submandibular gland in a 71-year-old male patient and present the associated imaging findings. The patient was considered to have a de novo type of myoepithelial carcinoma, which is reportedly associated with higher malignancy than the transformation type of the disease (i.e., a malignant change from pleomorphic adenoma or myoepithelioma). This was reflected in the multiple lung and bone metastases sites and strong positivity for p53 and Ki-67.