Sclerosing
mucoepidermoid carcinoma with
eosinophilia (SMCE) of the salivary gland is a rare variant of
mucoepidermoid carcinoma. We report a case of SMCE in the right submandibular gland of a 79-year-old man. Fine needle aspiration cytology revealed cohesive clusters of atypical squamous epithelial cells admixed with cells containing intracytoplasmic
mucin and eosinophils. Histologically, the
tumor was composed of epithelial nests with keratinizing cells occasionally present at the center, as well as peripherally located atypical basaloid cells, and some
mucin-containing cells embedded in a fibrosclerotic stroma, which were accompanied by a prominent lymphoplasmacytic and eosinophilic infiltrate. Inflammatory infiltrate and stromal fibrosclerosis also were seen in the non-neoplastic salivary gland tissue adjacent to the
tumor. Immunohistochemically, many plasma cells were IgG4-positive. The postoperative serum
IgG4 level was elevated. Our reverse transcription-polymerase chain reaction using
formalin-fixed,
paraffin-embedded
tumor tissue failed to detect any fusion-gene transcripts which are specifically identified in ordinary
mucoepidermoid carcinoma. The findings of the present case suggest that this rare type of salivary gland
carcinoma may be associated with a chronic inflammatory condition such as
IgG4-related sclerosing disease. Only 23 cases of sclerosing
mucoepidermoid carcinoma with or without eosinophilic infiltratie have been reported to date in such an anatomical location.