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Diagnosis and management of small pulmonary atypical carcinoid tumor associated with Cushing syndrome

Ectopic adrenocorticotropic hormone (ACTH) syndrome is rare and identification of its source is often challenging. We report the case of an ectopic Cushing syndrome in a young adult male secondary to an occult ACTH producing atypical carcinoid tumor. Extensive biochemical and imaging workup was unre...

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Autores principales: Benissan-Messan, Dathe Z, Merritt, Robert E, Shilo, Konstantin, D'Souza, Desmond M, Kneuertz, Peter J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729590/
https://www.ncbi.nlm.nih.gov/pubmed/33318759
http://dx.doi.org/10.2217/lmt-2020-0010
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author Benissan-Messan, Dathe Z
Merritt, Robert E
Shilo, Konstantin
D'Souza, Desmond M
Kneuertz, Peter J
author_facet Benissan-Messan, Dathe Z
Merritt, Robert E
Shilo, Konstantin
D'Souza, Desmond M
Kneuertz, Peter J
author_sort Benissan-Messan, Dathe Z
collection PubMed
description Ectopic adrenocorticotropic hormone (ACTH) syndrome is rare and identification of its source is often challenging. We report the case of an ectopic Cushing syndrome in a young adult male secondary to an occult ACTH producing atypical carcinoid tumor. Extensive biochemical and imaging workup was unrevealing. The diagnosis was aided by Ga-DOTA PET scan demonstrating a suspicious left upper lobe lung nodule. The patient underwent video-assisted thoracoscopic exploration with wedge resection and mediastinal lymphadenectomy of a T2aN2M0 atypical carcinoid, resulting in the normalization of ACTH levels and complete resolution of symptoms. The role of a Ga-DOTA PET scan in diagnosing pulmonary carcinoid tumors and their management are discussed.
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spelling pubmed-77295902020-12-13 Diagnosis and management of small pulmonary atypical carcinoid tumor associated with Cushing syndrome Benissan-Messan, Dathe Z Merritt, Robert E Shilo, Konstantin D'Souza, Desmond M Kneuertz, Peter J Lung Cancer Manag Case Report Ectopic adrenocorticotropic hormone (ACTH) syndrome is rare and identification of its source is often challenging. We report the case of an ectopic Cushing syndrome in a young adult male secondary to an occult ACTH producing atypical carcinoid tumor. Extensive biochemical and imaging workup was unrevealing. The diagnosis was aided by Ga-DOTA PET scan demonstrating a suspicious left upper lobe lung nodule. The patient underwent video-assisted thoracoscopic exploration with wedge resection and mediastinal lymphadenectomy of a T2aN2M0 atypical carcinoid, resulting in the normalization of ACTH levels and complete resolution of symptoms. The role of a Ga-DOTA PET scan in diagnosing pulmonary carcinoid tumors and their management are discussed. Future Medicine Ltd 2020-09-14 /pmc/articles/PMC7729590/ /pubmed/33318759 http://dx.doi.org/10.2217/lmt-2020-0010 Text en © 2020 Peter J Kneuertz This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Case Report
Benissan-Messan, Dathe Z
Merritt, Robert E
Shilo, Konstantin
D'Souza, Desmond M
Kneuertz, Peter J
Diagnosis and management of small pulmonary atypical carcinoid tumor associated with Cushing syndrome
title Diagnosis and management of small pulmonary atypical carcinoid tumor associated with Cushing syndrome
title_full Diagnosis and management of small pulmonary atypical carcinoid tumor associated with Cushing syndrome
title_fullStr Diagnosis and management of small pulmonary atypical carcinoid tumor associated with Cushing syndrome
title_full_unstemmed Diagnosis and management of small pulmonary atypical carcinoid tumor associated with Cushing syndrome
title_short Diagnosis and management of small pulmonary atypical carcinoid tumor associated with Cushing syndrome
title_sort diagnosis and management of small pulmonary atypical carcinoid tumor associated with cushing syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729590/
https://www.ncbi.nlm.nih.gov/pubmed/33318759
http://dx.doi.org/10.2217/lmt-2020-0010
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