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Hyponatraemia and hyperpigmentation in primary adrenal insufficiency

Hyponatraemia is a common electrolyte disturbance with multiple causes. We present a case of a 49-year-old Caucasian female with cholangiocarcinoma, who had a hyponatraemia which was initially assumed to be based on a syndrome of inappropriate antidiuretic hormone secretion as paraneoplastic phenome...

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Autores principales: Benner, Bernadette Johanna Maria, Alsma, Jelmer, Feelders, Richard A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6424183/
https://www.ncbi.nlm.nih.gov/pubmed/30850564
http://dx.doi.org/10.1136/bcr-2018-227200
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author Benner, Bernadette Johanna Maria
Alsma, Jelmer
Feelders, Richard A
author_facet Benner, Bernadette Johanna Maria
Alsma, Jelmer
Feelders, Richard A
author_sort Benner, Bernadette Johanna Maria
collection PubMed
description Hyponatraemia is a common electrolyte disturbance with multiple causes. We present a case of a 49-year-old Caucasian female with cholangiocarcinoma, who had a hyponatraemia which was initially assumed to be based on a syndrome of inappropriate antidiuretic hormone secretion as paraneoplastic phenomenon. At physical examination, hyperpigmentation was seen and multiple episodes with syncope were reported. Subsequent endocrine assessment with a synthetic adrenocorticotropin hormone (ACTH) stimulation test and measurement of ACTH levels revealed primary adrenal insufficiency also known as Morbus Addison. We started hydrocortisone and fludrocortisone replacement therapy, resulting in resolving of symptoms, hyponatraemia and hyperpigmentation.
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spelling pubmed-64241832019-04-05 Hyponatraemia and hyperpigmentation in primary adrenal insufficiency Benner, Bernadette Johanna Maria Alsma, Jelmer Feelders, Richard A BMJ Case Rep Reminder of Important Clinical Lesson Hyponatraemia is a common electrolyte disturbance with multiple causes. We present a case of a 49-year-old Caucasian female with cholangiocarcinoma, who had a hyponatraemia which was initially assumed to be based on a syndrome of inappropriate antidiuretic hormone secretion as paraneoplastic phenomenon. At physical examination, hyperpigmentation was seen and multiple episodes with syncope were reported. Subsequent endocrine assessment with a synthetic adrenocorticotropin hormone (ACTH) stimulation test and measurement of ACTH levels revealed primary adrenal insufficiency also known as Morbus Addison. We started hydrocortisone and fludrocortisone replacement therapy, resulting in resolving of symptoms, hyponatraemia and hyperpigmentation. BMJ Publishing Group 2019-03-07 /pmc/articles/PMC6424183/ /pubmed/30850564 http://dx.doi.org/10.1136/bcr-2018-227200 Text en © BMJ Publishing Group Limited 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Reminder of Important Clinical Lesson
Benner, Bernadette Johanna Maria
Alsma, Jelmer
Feelders, Richard A
Hyponatraemia and hyperpigmentation in primary adrenal insufficiency
title Hyponatraemia and hyperpigmentation in primary adrenal insufficiency
title_full Hyponatraemia and hyperpigmentation in primary adrenal insufficiency
title_fullStr Hyponatraemia and hyperpigmentation in primary adrenal insufficiency
title_full_unstemmed Hyponatraemia and hyperpigmentation in primary adrenal insufficiency
title_short Hyponatraemia and hyperpigmentation in primary adrenal insufficiency
title_sort hyponatraemia and hyperpigmentation in primary adrenal insufficiency
topic Reminder of Important Clinical Lesson
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6424183/
https://www.ncbi.nlm.nih.gov/pubmed/30850564
http://dx.doi.org/10.1136/bcr-2018-227200
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