Adrenocorticotropic hormone-secreting esthesioneuroblastoma with ectopic cushing’s syndrome

Young Soo Chung; Minkyun Na; Cheol Ryong Ku; Se Hoon Kim; Eui Hyun Kim

doi:10.3349/ymj.2020.61.3.257

Adrenocorticotropic hormone-secreting esthesioneuroblastoma with ectopic cushing’s syndrome

Young Soo Chung, Minkyun Na, Cheol Ryong Ku, Se Hoon Kim, Eui Hyun Kim

Department of Pathology

Research output: Contribution to journal › Article › peer-review

2 Citations (Scopus)

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.

Original language	English
Pages (from-to)	257-261
Number of pages	5
Journal	Yonsei medical journal
Volume	61
Issue number	3
DOIs	https://doi.org/10.3349/ymj.2020.61.3.257
Publication status	Published - 2020 Mar

Bibliographical note

Funding Information:
This study was funded by the Basic Science Research Program through the NRF of Korea (NRF-2018R1C1B5042687) from the Korean Ministry of Science, ICT and Future Planning and the “Dongwha” Faculty Research Assistance Program of Yonsei University College of Medicine (6-2018-0073).

Publisher Copyright:
© Yonsei University College of Medicine 2020.

All Science Journal Classification (ASJC) codes

Medicine(all)

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title = "Adrenocorticotropic hormone-secreting esthesioneuroblastoma with ectopic cushing{\textquoteright}s syndrome",

abstract = "Esthesioneuroblastoma as a source of ectopic Cushing{\textquoteright}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.",

author = "Chung, {Young Soo} and Minkyun Na and Ku, {Cheol Ryong} and Kim, {Se Hoon} and Kim, {Eui Hyun}",

note = "Funding Information: This study was funded by the Basic Science Research Program through the NRF of Korea (NRF-2018R1C1B5042687) from the Korean Ministry of Science, ICT and Future Planning and the “Dongwha” Faculty Research Assistance Program of Yonsei University College of Medicine (6-2018-0073). Publisher Copyright: {\textcopyright} Yonsei University College of Medicine 2020.",

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AU - Chung, Young Soo

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AU - Ku, Cheol Ryong

AU - Kim, Se Hoon

AU - Kim, Eui Hyun

N1 - Funding Information: This study was funded by the Basic Science Research Program through the NRF of Korea (NRF-2018R1C1B5042687) from the Korean Ministry of Science, ICT and Future Planning and the “Dongwha” Faculty Research Assistance Program of Yonsei University College of Medicine (6-2018-0073). Publisher Copyright: © Yonsei University College of Medicine 2020.

PY - 2020/3

Y1 - 2020/3

N2 - 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.

AB - 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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Adrenocorticotropic hormone-secreting esthesioneuroblastoma with ectopic cushing’s syndrome

Abstract

Bibliographical note

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