Adrenocorticotropic hormone-secreting esthesioneuroblastoma with ectopic cushing’s syndrome

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Abstract

Esthesioneuroblastoma as a source of ectopic Cushing’s syndrome is rare, and to the best of our knowledge, only 20 cases have been reported worldwide. A 46-year-old healthy man visited a local clinic for general weakness and hyposmia, and underwent examination with serial endocrinological workup and brain imaging.68Gallium-DOTA-TOC positron emission tomography scan was helpful where diagnosis of sellar MRI and inferior petrosal sinus sampling were discordant. Combined transcranial and endoscopic endonasal approach surgery was performed, and a diagnosis of esthesioneuroblastoma was given.

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Chung, Y. S., Na, M., Ku, C. R., Kim, S. H., & Kim, E. H. (2020). Adrenocorticotropic hormone-secreting esthesioneuroblastoma with ectopic cushing’s syndrome. Yonsei Medical Journal, 61(3), 257–261. https://doi.org/10.3349/ymj.2020.61.3.257

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