A Rare Case of Ectopic Adrenocorticotropic Hormone Secretion from Pancreatic Neuroendocrine Tumour Presenting with Cushing Syndrome

Ectopic adrenocorticotropic hormone secretion (EAS) from the pancreatic neuroendocrine tumour (PNET) is rare, aggressive, and challenging to treat. We hereby present a rare case of EAS from PNET presenting with Cushing syndrome diagnosed with endoscopic ultrasound-guided fine-needle aspiration cytol...

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Autores principales: Lee, Soon Liang, Ng, Chiun Yann, Sidhu, Jasminder, Awang, Asmawiza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2022
Materias:
Clinical Case Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305245/
https://www.ncbi.nlm.nih.gov/pubmed/37387716
http://dx.doi.org/10.1159/000521518
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author Lee, Soon Liang
Ng, Chiun Yann
Sidhu, Jasminder
Awang, Asmawiza
author_facet Lee, Soon Liang
Ng, Chiun Yann
Sidhu, Jasminder
Awang, Asmawiza
author_sort Lee, Soon Liang
collection PubMed
description Ectopic adrenocorticotropic hormone secretion (EAS) from the pancreatic neuroendocrine tumour (PNET) is rare, aggressive, and challenging to treat. We hereby present a rare case of EAS from PNET presenting with Cushing syndrome diagnosed with endoscopic ultrasound-guided fine-needle aspiration cytology. This case highlights the advanced presentation of EAS from PNET with poor clinical correlation of hypercortisolism and the grade of PNET.
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spelling pubmed-103052452023-06-29 A Rare Case of Ectopic Adrenocorticotropic Hormone Secretion from Pancreatic Neuroendocrine Tumour Presenting with Cushing Syndrome Lee, Soon Liang Ng, Chiun Yann Sidhu, Jasminder Awang, Asmawiza GE Port J Gastroenterol Clinical Case Study Ectopic adrenocorticotropic hormone secretion (EAS) from the pancreatic neuroendocrine tumour (PNET) is rare, aggressive, and challenging to treat. We hereby present a rare case of EAS from PNET presenting with Cushing syndrome diagnosed with endoscopic ultrasound-guided fine-needle aspiration cytology. This case highlights the advanced presentation of EAS from PNET with poor clinical correlation of hypercortisolism and the grade of PNET. S. Karger AG 2022-03-01 /pmc/articles/PMC10305245/ /pubmed/37387716 http://dx.doi.org/10.1159/000521518 Text en Copyright © 2022 by Sociedade Portuguesa de Gastrenterologia. Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC). Usage and distribution for commercial purposes requires written permission.
spellingShingle Clinical Case Study
Lee, Soon Liang
Ng, Chiun Yann
Sidhu, Jasminder
Awang, Asmawiza
A Rare Case of Ectopic Adrenocorticotropic Hormone Secretion from Pancreatic Neuroendocrine Tumour Presenting with Cushing Syndrome
title A Rare Case of Ectopic Adrenocorticotropic Hormone Secretion from Pancreatic Neuroendocrine Tumour Presenting with Cushing Syndrome
title_full A Rare Case of Ectopic Adrenocorticotropic Hormone Secretion from Pancreatic Neuroendocrine Tumour Presenting with Cushing Syndrome
title_fullStr A Rare Case of Ectopic Adrenocorticotropic Hormone Secretion from Pancreatic Neuroendocrine Tumour Presenting with Cushing Syndrome
title_full_unstemmed A Rare Case of Ectopic Adrenocorticotropic Hormone Secretion from Pancreatic Neuroendocrine Tumour Presenting with Cushing Syndrome
title_short A Rare Case of Ectopic Adrenocorticotropic Hormone Secretion from Pancreatic Neuroendocrine Tumour Presenting with Cushing Syndrome
title_sort rare case of ectopic adrenocorticotropic hormone secretion from pancreatic neuroendocrine tumour presenting with cushing syndrome
topic Clinical Case Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305245/
https://www.ncbi.nlm.nih.gov/pubmed/37387716
http://dx.doi.org/10.1159/000521518
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