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Cushing´s syndrome: high aggressiveness of low-grade tumors

Cushing´s syndrome is caused by prolonged exposition supraphysiological to endogenous or exogenous cortisol. Ectopic production of adrenocorticotropic hormone by lung carcinoid tumors is relatively rare. Most documented cases have been reported individually. This rare neoplasm low grade that may sec...

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Autores principales: Guendouz, Faycal El, Derrou, Sara, Atoini, Fouad, Ouleghzal, Hassan, Safi, Somaya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603813/
https://www.ncbi.nlm.nih.gov/pubmed/33193969
http://dx.doi.org/10.11604/pamj.2020.36.315.23901
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author Guendouz, Faycal El
Derrou, Sara
Atoini, Fouad
Ouleghzal, Hassan
Safi, Somaya
author_facet Guendouz, Faycal El
Derrou, Sara
Atoini, Fouad
Ouleghzal, Hassan
Safi, Somaya
author_sort Guendouz, Faycal El
collection PubMed
description Cushing´s syndrome is caused by prolonged exposition supraphysiological to endogenous or exogenous cortisol. Ectopic production of adrenocorticotropic hormone by lung carcinoid tumors is relatively rare. Most documented cases have been reported individually. This rare neoplasm low grade that may secrete adrenocorticotropin (ACTH) leading to rapid development of hypercortisolism which is the main mode of discovery, can be a real aggressive form. This report shows a high aggressiveness of this endocrine neoplasia, wich was marked on the general, morphological, bone and psychiatric level. The trivialization of clinical signs had caused the delay in diagnosis with irreparable bone consequences.
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spelling pubmed-76038132020-11-12 Cushing´s syndrome: high aggressiveness of low-grade tumors Guendouz, Faycal El Derrou, Sara Atoini, Fouad Ouleghzal, Hassan Safi, Somaya Pan Afr Med J Case Report Cushing´s syndrome is caused by prolonged exposition supraphysiological to endogenous or exogenous cortisol. Ectopic production of adrenocorticotropic hormone by lung carcinoid tumors is relatively rare. Most documented cases have been reported individually. This rare neoplasm low grade that may secrete adrenocorticotropin (ACTH) leading to rapid development of hypercortisolism which is the main mode of discovery, can be a real aggressive form. This report shows a high aggressiveness of this endocrine neoplasia, wich was marked on the general, morphological, bone and psychiatric level. The trivialization of clinical signs had caused the delay in diagnosis with irreparable bone consequences. The African Field Epidemiology Network 2020-08-21 /pmc/articles/PMC7603813/ /pubmed/33193969 http://dx.doi.org/10.11604/pamj.2020.36.315.23901 Text en Copyright: Faycal El Guendouz et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Guendouz, Faycal El
Derrou, Sara
Atoini, Fouad
Ouleghzal, Hassan
Safi, Somaya
Cushing´s syndrome: high aggressiveness of low-grade tumors
title Cushing´s syndrome: high aggressiveness of low-grade tumors
title_full Cushing´s syndrome: high aggressiveness of low-grade tumors
title_fullStr Cushing´s syndrome: high aggressiveness of low-grade tumors
title_full_unstemmed Cushing´s syndrome: high aggressiveness of low-grade tumors
title_short Cushing´s syndrome: high aggressiveness of low-grade tumors
title_sort cushing´s syndrome: high aggressiveness of low-grade tumors
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603813/
https://www.ncbi.nlm.nih.gov/pubmed/33193969
http://dx.doi.org/10.11604/pamj.2020.36.315.23901
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