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Acromegaly and Cushing's syndrome caused by a neuroendocrine tumor arising within a sacrococcygeal teratoma
A 60‐year‐old man with a pre‐existing stable sacrococcygeal teratoma developed acromegaly, ectopic Cushing's syndrome, and 5HIAA secretion. To our knowledge, this represents the first reported case of ACTH and serotonin secretion, and likely GHRH or GH cosecretion, from a sacrococcygeal teratom...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676263/ https://www.ncbi.nlm.nih.gov/pubmed/29152267 http://dx.doi.org/10.1002/ccr3.1148 |
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author | Babiker, Tarig Kyrodimou, Efstathia Berney, Daniel M. Gurnell, Mark Drake, William M. Brooke, Antonia |
author_facet | Babiker, Tarig Kyrodimou, Efstathia Berney, Daniel M. Gurnell, Mark Drake, William M. Brooke, Antonia |
author_sort | Babiker, Tarig |
collection | PubMed |
description | A 60‐year‐old man with a pre‐existing stable sacrococcygeal teratoma developed acromegaly, ectopic Cushing's syndrome, and 5HIAA secretion. To our knowledge, this represents the first reported case of ACTH and serotonin secretion, and likely GHRH or GH cosecretion, from a sacrococcygeal teratoma in an adult. |
format | Online Article Text |
id | pubmed-5676263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56762632017-11-17 Acromegaly and Cushing's syndrome caused by a neuroendocrine tumor arising within a sacrococcygeal teratoma Babiker, Tarig Kyrodimou, Efstathia Berney, Daniel M. Gurnell, Mark Drake, William M. Brooke, Antonia Clin Case Rep Case Reports A 60‐year‐old man with a pre‐existing stable sacrococcygeal teratoma developed acromegaly, ectopic Cushing's syndrome, and 5HIAA secretion. To our knowledge, this represents the first reported case of ACTH and serotonin secretion, and likely GHRH or GH cosecretion, from a sacrococcygeal teratoma in an adult. John Wiley and Sons Inc. 2017-09-14 /pmc/articles/PMC5676263/ /pubmed/29152267 http://dx.doi.org/10.1002/ccr3.1148 Text en © 2017 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Babiker, Tarig Kyrodimou, Efstathia Berney, Daniel M. Gurnell, Mark Drake, William M. Brooke, Antonia Acromegaly and Cushing's syndrome caused by a neuroendocrine tumor arising within a sacrococcygeal teratoma |
title | Acromegaly and Cushing's syndrome caused by a neuroendocrine tumor arising within a sacrococcygeal teratoma |
title_full | Acromegaly and Cushing's syndrome caused by a neuroendocrine tumor arising within a sacrococcygeal teratoma |
title_fullStr | Acromegaly and Cushing's syndrome caused by a neuroendocrine tumor arising within a sacrococcygeal teratoma |
title_full_unstemmed | Acromegaly and Cushing's syndrome caused by a neuroendocrine tumor arising within a sacrococcygeal teratoma |
title_short | Acromegaly and Cushing's syndrome caused by a neuroendocrine tumor arising within a sacrococcygeal teratoma |
title_sort | acromegaly and cushing's syndrome caused by a neuroendocrine tumor arising within a sacrococcygeal teratoma |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676263/ https://www.ncbi.nlm.nih.gov/pubmed/29152267 http://dx.doi.org/10.1002/ccr3.1148 |
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