| Mucoepidermoid carcinoma | |
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| Classification and external resources | |
Micrograph of a mucoepidermoid carcinoma. FNA specimen. Pap stain. |
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| ICD-O: | 8430/3 |
| OMIM | 607536 |
| MeSH | C04.557.470.200.025.340 |
Mucoepidermoid carcinoma is the most common type of salivary gland malignancy in adults. Mucoepidermoid carcinoma can also be found in other organs, as bronchi, lacrimal sac [1] and thyroid.
Mucicarmine staining is one stain used by pathologist for detection.[2]
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Contents
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Occurs in adults, with peak incidence from 20–40 years of age. A causal link with cytomegalovirus (CMV) has been strongly implicated in a 2011 research.[3]
Presents as painless, slow-growing mass that is firm or hard. Most appear clinically as mixed tumors.
This tumor is not encapsulated and is characterized by squamous cells, mucus-secreting cells, and intermediate cells.
Mucoepidermoid carcinomas of the salivary and bronchial glands are characterized by a recurrent t(11;19)(q21;p13) chromosomal translocation resulting in a MECT1-MAML2 fusion gene. The CREB-binding domain of the CREB coactivator MECT1 (also known as CRTC1, TORC1 or WAMTP1) is fused to the transactivation domain of the Notch coactivator MAML2 PMID 16444749.
Generally, there is a good prognosis for low-grade tumors, and a poor prognosis for high-grade tumors.
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