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Ectopic Cushing's Syndrome Secondary to Metastatic Paraganglioma

Paraneoplastic or ectopic Cushing's syndrome (CS) is a rare cause of endogenous hypercortisolism. It is due to ectopic adrenocorticotropic hormone (ACTH) secretion and has been reported in association with a variety of neuroendocrine tumors such as small-cell lung carcinoma, carcinoid tumors, a...

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Autores principales: Daya, R., Wingfield, C., Sotshononda, P., Seedat, F., Bulbulia, S., Simmons, M. D., Louw, M., Bayat, Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249138/
https://www.ncbi.nlm.nih.gov/pubmed/34258082
http://dx.doi.org/10.1155/2021/5593920
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author Daya, R.
Wingfield, C.
Sotshononda, P.
Seedat, F.
Bulbulia, S.
Simmons, M. D.
Louw, M.
Bayat, Z.
author_facet Daya, R.
Wingfield, C.
Sotshononda, P.
Seedat, F.
Bulbulia, S.
Simmons, M. D.
Louw, M.
Bayat, Z.
author_sort Daya, R.
collection PubMed
description Paraneoplastic or ectopic Cushing's syndrome (CS) is a rare cause of endogenous hypercortisolism. It is due to ectopic adrenocorticotropic hormone (ACTH) secretion and has been reported in association with a variety of neuroendocrine tumors such as small-cell lung carcinoma, carcinoid tumors, and medullary carcinoma of the thyroid. Paragangliomas (PGLs) are rare neuroendocrine tumors that can secrete catecholamines. Case reports and reports of ectopic ACTH secretion from metastatic PGLs causing CS are exceedingly rare. We present a case of a 38-year-old female, who presented with typical signs, symptoms, and complications of CS, secondary to a PGL with widespread metastases, which eventually led to her demise.
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spelling pubmed-82491382021-07-12 Ectopic Cushing's Syndrome Secondary to Metastatic Paraganglioma Daya, R. Wingfield, C. Sotshononda, P. Seedat, F. Bulbulia, S. Simmons, M. D. Louw, M. Bayat, Z. Case Rep Endocrinol Case Report Paraneoplastic or ectopic Cushing's syndrome (CS) is a rare cause of endogenous hypercortisolism. It is due to ectopic adrenocorticotropic hormone (ACTH) secretion and has been reported in association with a variety of neuroendocrine tumors such as small-cell lung carcinoma, carcinoid tumors, and medullary carcinoma of the thyroid. Paragangliomas (PGLs) are rare neuroendocrine tumors that can secrete catecholamines. Case reports and reports of ectopic ACTH secretion from metastatic PGLs causing CS are exceedingly rare. We present a case of a 38-year-old female, who presented with typical signs, symptoms, and complications of CS, secondary to a PGL with widespread metastases, which eventually led to her demise. Hindawi 2021-06-24 /pmc/articles/PMC8249138/ /pubmed/34258082 http://dx.doi.org/10.1155/2021/5593920 Text en Copyright © 2021 R. Daya et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Daya, R.
Wingfield, C.
Sotshononda, P.
Seedat, F.
Bulbulia, S.
Simmons, M. D.
Louw, M.
Bayat, Z.
Ectopic Cushing's Syndrome Secondary to Metastatic Paraganglioma
title Ectopic Cushing's Syndrome Secondary to Metastatic Paraganglioma
title_full Ectopic Cushing's Syndrome Secondary to Metastatic Paraganglioma
title_fullStr Ectopic Cushing's Syndrome Secondary to Metastatic Paraganglioma
title_full_unstemmed Ectopic Cushing's Syndrome Secondary to Metastatic Paraganglioma
title_short Ectopic Cushing's Syndrome Secondary to Metastatic Paraganglioma
title_sort ectopic cushing's syndrome secondary to metastatic paraganglioma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249138/
https://www.ncbi.nlm.nih.gov/pubmed/34258082
http://dx.doi.org/10.1155/2021/5593920
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