AI Article Synopsis

  • A case of sclerosing mucoepidermoid carcinoma (MEC) was reported in a 73-year-old woman, presenting as a mass in the parotid gland.
  • Imaging showed a well-defined 25 mm tumor with calcifications, extending into nearby spaces, indicating aggressive behavior.
  • Molecular analysis confirmed the presence of the CRTC1-MAML2 gene fusion, marking the first identification of this genetic association in sclerosing MEC, which strengthens the link between the two cancer types.

Article Abstract

In this article, we report a case of sclerosing mucoepidermoid carcinoma (MEC) arising in the parotid gland, with CRTC1-MAML2 gene fusion. A 73-year-old woman with a mass in the right parotid region was referred to our hospital. Radiological imaging tests revealed a well-defined mass, measuring 25 mm in diameter, with foci of calcification in the deep lobe of the parotid gland, extending to the parapharyngeal space. Microscopically, the tumor was composed of a proliferation of atypical glandular epithelial cells having intracytoplasmic mucin, squamoid cells, and intermediate cells arranged in nests embedded in a fibrosclerotic stroma, associated with a dense chronic inflammatory infiltrate containing immunoglobulin G4-immunoreactive plasma cells. Reverse transcription-polymerase chain reaction analysis using a formalin-fixed, paraffin-embedded tumor tissue specimen revealed the CRTC1-MAML2 fusion gene transcript. This is the first report of sclerosing MEC with the detection of the MEC-associated fusion gene, reinforcing a common genetic association between MEC and sclerosing MEC.

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Source
http://dx.doi.org/10.1177/1066896917742721DOI Listing

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