Abstract
Objective: As neuroendocrine carcinomas in the head and neck region are extremely rare, their clinicopathological characteristics remain largely unknown. Moreover, the 2005World Health Organization classification criteria for head and neck carcinomas with neuroendocrine features have numerous limitations. Therefore, the clinicopathological features and patient outcomes of these tumors must be clarified. Methods: Between 2007 and 2012, we encountered nine cases of head and neck cancer involving a neuroendocrine carcinoma component. We investigated these tumors according to the 2010 World Health Organization classification criteria for neuroendocrine tumors, and their clinicopathological characteristics and clinical outcomes were examined. Results: Carcinomas with neuroendocrine features were found to have an aggressive clinical course, which corresponded with the Ki-67 index and mitotic count. Conclusions: Owing to the difficulty in appropriately diagnosing head and neck carcinomas with neuroendocrine features using the current classification system, a new classification system should be developed for use in these cases.
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Hamamoto, T., Fujii, S., Miyazaki, M., Shinozaki, T., Tomioka, T., & Hayashi, R. (2015). Nine cases of carcinoma with neuroendocrine features in the head and neck: Clinicopathological characteristics and clinical outcomes. Japanese Journal of Clinical Oncology, 45(4), 328–335. https://doi.org/10.1093/jjco/hyv008
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