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Adrenal ganglioneuroma: What you need to know

Adrenal ganglioneuromas (GNs) constitute rare, differentiated tumors which originate from neural crest cells. GNs are usually hormonally silent and tend to be discovered incidentally on imaging tests. Adrenalectomy is the gold standard for the treatment of primary adrenal GNs. Nevertheless, preopera...

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Autores principales: Mylonas, Konstantinos S, Schizas, Dimitrios, Economopoulos, Konstantinos P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648998/
https://www.ncbi.nlm.nih.gov/pubmed/29085827
http://dx.doi.org/10.12998/wjcc.v5.i10.373
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author Mylonas, Konstantinos S
Schizas, Dimitrios
Economopoulos, Konstantinos P
author_facet Mylonas, Konstantinos S
Schizas, Dimitrios
Economopoulos, Konstantinos P
author_sort Mylonas, Konstantinos S
collection PubMed
description Adrenal ganglioneuromas (GNs) constitute rare, differentiated tumors which originate from neural crest cells. GNs are usually hormonally silent and tend to be discovered incidentally on imaging tests. Adrenalectomy is the gold standard for the treatment of primary adrenal GNs. Nevertheless, preoperative differential diagnosis of GNs remains extremely challenging, and thus histopathological examination is required in order to confirm the diagnosis of GN. Overall, prognosis after surgical resection seems to be excellent, without any recurrences or need for adjuvant therapy.
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spelling pubmed-56489982017-10-30 Adrenal ganglioneuroma: What you need to know Mylonas, Konstantinos S Schizas, Dimitrios Economopoulos, Konstantinos P World J Clin Cases Minireviews Adrenal ganglioneuromas (GNs) constitute rare, differentiated tumors which originate from neural crest cells. GNs are usually hormonally silent and tend to be discovered incidentally on imaging tests. Adrenalectomy is the gold standard for the treatment of primary adrenal GNs. Nevertheless, preoperative differential diagnosis of GNs remains extremely challenging, and thus histopathological examination is required in order to confirm the diagnosis of GN. Overall, prognosis after surgical resection seems to be excellent, without any recurrences or need for adjuvant therapy. Baishideng Publishing Group Inc 2017-10-16 2017-10-16 /pmc/articles/PMC5648998/ /pubmed/29085827 http://dx.doi.org/10.12998/wjcc.v5.i10.373 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Minireviews
Mylonas, Konstantinos S
Schizas, Dimitrios
Economopoulos, Konstantinos P
Adrenal ganglioneuroma: What you need to know
title Adrenal ganglioneuroma: What you need to know
title_full Adrenal ganglioneuroma: What you need to know
title_fullStr Adrenal ganglioneuroma: What you need to know
title_full_unstemmed Adrenal ganglioneuroma: What you need to know
title_short Adrenal ganglioneuroma: What you need to know
title_sort adrenal ganglioneuroma: what you need to know
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648998/
https://www.ncbi.nlm.nih.gov/pubmed/29085827
http://dx.doi.org/10.12998/wjcc.v5.i10.373
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