Primary Carcinoid Tumor in the External Auditory Canal

Dong Hae Chung, Kyu Cheol Han, Na Rae Kim
<span title="2019-11-13">2019</span> <i title="The Korean Society of Pathologists and The Korean Society for Cytopathology"> <a target="_blank" rel="noopener" href="" style="color: black;">Journal of Pathology and Translational Medicine</a> </i> &nbsp;
A 39-year-old man visited the department of otolaryngology due to an ongoing hearing disturbance that had lasted for 1 year. Temporal bone computed tomography revealed soft tissue density nearly obliterating the left external auditory canal (EAC). The mass was composed of sheets of round tumor cells containing moderate amounts of fine granular cytoplasm and salt and pepper chromatin. Neither mitosis nor necrosis was found. The Ki-67 proliferation index was less than 2%. Cells were positive for
more &raquo; ... D56 and synaptophysin but negative for chromogranin, cytokeratin (CK) 20, and CK7. Based on these findings, the tumor was diagnosed as a carcinoid tumor, well differentiated neuroendocrine carcinoma, grade 1 (G1) according to current World Health Organization (WHO) classification of head and neck tumors; and a neuroendocrine tumor, G1 according to neuroendocrine neoplasm (NEN)-2018 WHO standard classification. He remained free of local recurrence and metastasis after 20 months of follow up. To date, only six cases of primary NENs in the EAC have been reported. Metastatic tumor should be included in the differential diagnoses. Because of its rarity, the prognosis and treatment have not yet been clarified.
<span class="external-identifiers"> <a target="_blank" rel="external noopener noreferrer" href="">doi:10.4132/jptm.2019.11.07</a> <a target="_blank" rel="external noopener" href="">pmid:31718119</a> <a target="_blank" rel="external noopener" href="">pmcid:PMC7093287</a> <a target="_blank" rel="external noopener" href="">fatcat:fyadshoqj5b5bf3rwm2sgb75ma</a> </span>
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