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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...

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Detalles Bibliográficos
Autores principales: Babiker, Tarig, Kyrodimou, Efstathia, Berney, Daniel M., Gurnell, Mark, Drake, William M., Brooke, Antonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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.
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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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