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Aldosterone-Secreting Adrenocortical Carcinoma Presenting With Cardiac Arrest

Adrenocortical carcinoma (ACC) is a rare malignancy that usually is detected as a result of symptoms of hormone excess or mass effect. We describe a rare presentation of ACC with primary aldosterone production leading to profound hypokalemia and cardiac arrest. The patient was previously asymptomati...

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Autores principales: Zern, Nicole K, Eaton, Keith D, Roth, Mara Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698141/
https://www.ncbi.nlm.nih.gov/pubmed/31440735
http://dx.doi.org/10.1210/js.2019-00092
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author Zern, Nicole K
Eaton, Keith D
Roth, Mara Y
author_facet Zern, Nicole K
Eaton, Keith D
Roth, Mara Y
author_sort Zern, Nicole K
collection PubMed
description Adrenocortical carcinoma (ACC) is a rare malignancy that usually is detected as a result of symptoms of hormone excess or mass effect. We describe a rare presentation of ACC with primary aldosterone production leading to profound hypokalemia and cardiac arrest. The patient was previously asymptomatic with low-grade, untreated hypertension and no documented electrolyte abnormalities. She had sudden cardiac arrest, and potassium levels were undetectable. After successful resuscitation, imaging showed a 6-cm left adrenal mass highly suspicious for malignancy. Biochemical workup revealed aldosterone excess as well as cortisol excess, despite the absence of Cushingoid symptoms. Histopathological examination after surgical resection demonstrated high-grade ACC. This case illustrates that the workup of cardiac arrest as a result of electrolyte abnormalities should include evaluation for adrenal pathology.
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spelling pubmed-66981412019-08-22 Aldosterone-Secreting Adrenocortical Carcinoma Presenting With Cardiac Arrest Zern, Nicole K Eaton, Keith D Roth, Mara Y J Endocr Soc Case Report Adrenocortical carcinoma (ACC) is a rare malignancy that usually is detected as a result of symptoms of hormone excess or mass effect. We describe a rare presentation of ACC with primary aldosterone production leading to profound hypokalemia and cardiac arrest. The patient was previously asymptomatic with low-grade, untreated hypertension and no documented electrolyte abnormalities. She had sudden cardiac arrest, and potassium levels were undetectable. After successful resuscitation, imaging showed a 6-cm left adrenal mass highly suspicious for malignancy. Biochemical workup revealed aldosterone excess as well as cortisol excess, despite the absence of Cushingoid symptoms. Histopathological examination after surgical resection demonstrated high-grade ACC. This case illustrates that the workup of cardiac arrest as a result of electrolyte abnormalities should include evaluation for adrenal pathology. Endocrine Society 2019-06-12 /pmc/articles/PMC6698141/ /pubmed/31440735 http://dx.doi.org/10.1210/js.2019-00092 Text en Copyright © 2019 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Zern, Nicole K
Eaton, Keith D
Roth, Mara Y
Aldosterone-Secreting Adrenocortical Carcinoma Presenting With Cardiac Arrest
title Aldosterone-Secreting Adrenocortical Carcinoma Presenting With Cardiac Arrest
title_full Aldosterone-Secreting Adrenocortical Carcinoma Presenting With Cardiac Arrest
title_fullStr Aldosterone-Secreting Adrenocortical Carcinoma Presenting With Cardiac Arrest
title_full_unstemmed Aldosterone-Secreting Adrenocortical Carcinoma Presenting With Cardiac Arrest
title_short Aldosterone-Secreting Adrenocortical Carcinoma Presenting With Cardiac Arrest
title_sort aldosterone-secreting adrenocortical carcinoma presenting with cardiac arrest
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698141/
https://www.ncbi.nlm.nih.gov/pubmed/31440735
http://dx.doi.org/10.1210/js.2019-00092
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