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

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Abstract

Salivary gland carcinomas are rare tumors, representing ~0.5% of all malignancies. Myoepithelioma is also 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.

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Santos, K. C. P., Matsuzaki, H., Unetsubo, T., Tsuyoshi, S., Nagatsuka, H., & Asaumi, J. I. (2017). De novo myoepithelial carcinoma with multiple metastases arising from a submandibular salivary gland: A case report. Oncology Letters, 13(4), 2679–2683. https://doi.org/10.3892/ol.2017.5783

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