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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2020
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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. |
format | Online Article Text |
id | pubmed-7603813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
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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