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Review

Pulmonary mucoepidermoid carcinoma: diagnosis and treatment

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Pages 249-255 | Received 20 Nov 2017, Accepted 12 Jan 2018, Published online: 17 Jan 2018
 

ABSTRACT

Introduction: Primary mucoepidermoid carcinomas (MEC) of the lung are rare and represent a diagnostic challenge. MEC in the lung is under the umbrella of primary salivary gland type tumors of the lung.

Areas covered: In general, salivary gland type tumors are represented by malignant neoplasms that may range from low to intermediate to high-grade type of malignancy sharing similar histopathological features as those in salivary glands. The focus in this review will be on one tumor in particular – mucoepidermoid carcinoma. Clinical, radiological, histopathological, and molecular diagnostic features will be highlighted in order to provide an insight on this unusual tumor in the lung. In addition, the treatment of these tumors will be discussed.

Expert commentary: It is important to stress that in the majority of cases, the proper use of histopathological assessment is the most important step in arriving at an accurate diagnosis. It is also important to recognized that there are other unusual primary tumoral conditions of the lung, which may pose a significant challenge in the differential diagnosis. The importance of proper recognition of mucoepidermoid carcinoma and its grading will be highlighted in order to assess clinical outcome.

Declaration of interest

The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties. Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.

Additional information

Funding

This manuscript has not received funding.

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