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Cushing Syndrome Secondary to Primary Neuroendocrine Lung Carcinoma

Cushing syndrome (CS) is a disorder characterized by a result of chronic exposure to excessive glucocorticoids. This article describes a case of a 30-year-old female presenting with fatigue, abdominal striae, unintentional weight gain, and lipodystrophy. A rare diagnosis of ectopic adrenocorticotrop...

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Detalles Bibliográficos
Autores principales: Zainal, A., Akinsola, O., Rajamani, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681596/
https://www.ncbi.nlm.nih.gov/pubmed/31428483
http://dx.doi.org/10.1155/2019/1989260
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author Zainal, A.
Akinsola, O.
Rajamani, K.
author_facet Zainal, A.
Akinsola, O.
Rajamani, K.
author_sort Zainal, A.
collection PubMed
description Cushing syndrome (CS) is a disorder characterized by a result of chronic exposure to excessive glucocorticoids. This article describes a case of a 30-year-old female presenting with fatigue, abdominal striae, unintentional weight gain, and lipodystrophy. A rare diagnosis of ectopic adrenocorticotropic-dependent CS was determined and a neuroendocrine lung tumor (NET) was discovered on chest x-ray. After surgical resection, pathology confirmed lung NET that stained positive for adrenocorticotropic hormone (ACTH). The patient's symptoms fully resolved. The authors aim to urge clinicians to maintain a high index of suspicion for ectopic ACTH secretion (EAS) through a multimodal approach when caring for patients with CS.
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spelling pubmed-66815962019-08-19 Cushing Syndrome Secondary to Primary Neuroendocrine Lung Carcinoma Zainal, A. Akinsola, O. Rajamani, K. Case Rep Endocrinol Case Report Cushing syndrome (CS) is a disorder characterized by a result of chronic exposure to excessive glucocorticoids. This article describes a case of a 30-year-old female presenting with fatigue, abdominal striae, unintentional weight gain, and lipodystrophy. A rare diagnosis of ectopic adrenocorticotropic-dependent CS was determined and a neuroendocrine lung tumor (NET) was discovered on chest x-ray. After surgical resection, pathology confirmed lung NET that stained positive for adrenocorticotropic hormone (ACTH). The patient's symptoms fully resolved. The authors aim to urge clinicians to maintain a high index of suspicion for ectopic ACTH secretion (EAS) through a multimodal approach when caring for patients with CS. Hindawi 2019-07-24 /pmc/articles/PMC6681596/ /pubmed/31428483 http://dx.doi.org/10.1155/2019/1989260 Text en Copyright © 2019 A. Zainal 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
Zainal, A.
Akinsola, O.
Rajamani, K.
Cushing Syndrome Secondary to Primary Neuroendocrine Lung Carcinoma
title Cushing Syndrome Secondary to Primary Neuroendocrine Lung Carcinoma
title_full Cushing Syndrome Secondary to Primary Neuroendocrine Lung Carcinoma
title_fullStr Cushing Syndrome Secondary to Primary Neuroendocrine Lung Carcinoma
title_full_unstemmed Cushing Syndrome Secondary to Primary Neuroendocrine Lung Carcinoma
title_short Cushing Syndrome Secondary to Primary Neuroendocrine Lung Carcinoma
title_sort cushing syndrome secondary to primary neuroendocrine lung carcinoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681596/
https://www.ncbi.nlm.nih.gov/pubmed/31428483
http://dx.doi.org/10.1155/2019/1989260
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AT akinsolao cushingsyndromesecondarytoprimaryneuroendocrinelungcarcinoma
AT rajamanik cushingsyndromesecondarytoprimaryneuroendocrinelungcarcinoma