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Cyclic ACTH-secreting thymic carcinoid: a case report and review of the literature

Cyclic Cushing's syndrome (CS) due to thymic carcinoid is a rare disorder. We report a case of cyclic CS due to ectopic adrenocorticotropic hormone (ACTH)-secreting atypical thymic carcinoid tumor and reviewed similar cases published in the literature. Our patient had hypercortisolemia lasting...

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Autores principales: Lamback, Elisa B., de Almeida, Sérgio Altino, Terra, Ricardo, Ferreira, Carlos Gil, Capelozzi, Vera Luiza, Haddad, Rui, Gadelha, Mônica R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Endocrinologia e Metabologia 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522176/
https://www.ncbi.nlm.nih.gov/pubmed/33844892
http://dx.doi.org/10.20945/2359-3997000000346
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author Lamback, Elisa B.
de Almeida, Sérgio Altino
Terra, Ricardo
Ferreira, Carlos Gil
Capelozzi, Vera Luiza
Haddad, Rui
Gadelha, Mônica R.
author_facet Lamback, Elisa B.
de Almeida, Sérgio Altino
Terra, Ricardo
Ferreira, Carlos Gil
Capelozzi, Vera Luiza
Haddad, Rui
Gadelha, Mônica R.
author_sort Lamback, Elisa B.
collection PubMed
description Cyclic Cushing's syndrome (CS) due to thymic carcinoid is a rare disorder. We report a case of cyclic CS due to ectopic adrenocorticotropic hormone (ACTH)-secreting atypical thymic carcinoid tumor and reviewed similar cases published in the literature. Our patient had hypercortisolemia lasting approximately one month, followed by normal cortisol secretion, with relapse one year later. Histopathology revealed an atypical ACTH-positive thymic carcinoid. Ectopic CS can be derived from atypical thymic carcinoids, which can be aggressive tumors with early relapse, suggesting that this type of tumor probably needs aggressive treatment.
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spelling pubmed-105221762023-09-27 Cyclic ACTH-secreting thymic carcinoid: a case report and review of the literature Lamback, Elisa B. de Almeida, Sérgio Altino Terra, Ricardo Ferreira, Carlos Gil Capelozzi, Vera Luiza Haddad, Rui Gadelha, Mônica R. Arch Endocrinol Metab Case Report Cyclic Cushing's syndrome (CS) due to thymic carcinoid is a rare disorder. We report a case of cyclic CS due to ectopic adrenocorticotropic hormone (ACTH)-secreting atypical thymic carcinoid tumor and reviewed similar cases published in the literature. Our patient had hypercortisolemia lasting approximately one month, followed by normal cortisol secretion, with relapse one year later. Histopathology revealed an atypical ACTH-positive thymic carcinoid. Ectopic CS can be derived from atypical thymic carcinoids, which can be aggressive tumors with early relapse, suggesting that this type of tumor probably needs aggressive treatment. Sociedade Brasileira de Endocrinologia e Metabologia 2021-04-12 /pmc/articles/PMC10522176/ /pubmed/33844892 http://dx.doi.org/10.20945/2359-3997000000346 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of 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
Lamback, Elisa B.
de Almeida, Sérgio Altino
Terra, Ricardo
Ferreira, Carlos Gil
Capelozzi, Vera Luiza
Haddad, Rui
Gadelha, Mônica R.
Cyclic ACTH-secreting thymic carcinoid: a case report and review of the literature
title Cyclic ACTH-secreting thymic carcinoid: a case report and review of the literature
title_full Cyclic ACTH-secreting thymic carcinoid: a case report and review of the literature
title_fullStr Cyclic ACTH-secreting thymic carcinoid: a case report and review of the literature
title_full_unstemmed Cyclic ACTH-secreting thymic carcinoid: a case report and review of the literature
title_short Cyclic ACTH-secreting thymic carcinoid: a case report and review of the literature
title_sort cyclic acth-secreting thymic carcinoid: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522176/
https://www.ncbi.nlm.nih.gov/pubmed/33844892
http://dx.doi.org/10.20945/2359-3997000000346
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