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Harlequin Syndrome Following Resection of Mediastinal Ganglioneuroma

Harlequin syndrome is a rare disorder of the sympathetic nervous system characterized by unilateral facial flushing and sweating. Although its etiology is unknown, this syndrome appears to be a dysfunction of the autonomic nervous system. To the best of our knowledge, thus far, very few reports on p...

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Detalles Bibliográficos
Autores principales: Jeon, Yeong Jeong, Son, Jongbae, Cho, Jong Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Thoracic and Cardiovascular Surgery 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380209/
https://www.ncbi.nlm.nih.gov/pubmed/28382275
http://dx.doi.org/10.5090/kjtcs.2017.50.2.130
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author Jeon, Yeong Jeong
Son, Jongbae
Cho, Jong Ho
author_facet Jeon, Yeong Jeong
Son, Jongbae
Cho, Jong Ho
author_sort Jeon, Yeong Jeong
collection PubMed
description Harlequin syndrome is a rare disorder of the sympathetic nervous system characterized by unilateral facial flushing and sweating. Although its etiology is unknown, this syndrome appears to be a dysfunction of the autonomic nervous system. To the best of our knowledge, thus far, very few reports on perioperative Harlequin syndrome after thoracic surgery have been published in the thoracic surgical literature. Here, we present the case of a 6-year-old patient who developed this unusual syndrome following the resection of a posterior mediastinal mass.
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spelling pubmed-53802092017-04-05 Harlequin Syndrome Following Resection of Mediastinal Ganglioneuroma Jeon, Yeong Jeong Son, Jongbae Cho, Jong Ho Korean J Thorac Cardiovasc Surg Case Report Harlequin syndrome is a rare disorder of the sympathetic nervous system characterized by unilateral facial flushing and sweating. Although its etiology is unknown, this syndrome appears to be a dysfunction of the autonomic nervous system. To the best of our knowledge, thus far, very few reports on perioperative Harlequin syndrome after thoracic surgery have been published in the thoracic surgical literature. Here, we present the case of a 6-year-old patient who developed this unusual syndrome following the resection of a posterior mediastinal mass. The Korean Society for Thoracic and Cardiovascular Surgery 2017-04 2017-04-05 /pmc/articles/PMC5380209/ /pubmed/28382275 http://dx.doi.org/10.5090/kjtcs.2017.50.2.130 Text en Copyright © 2017 by The Korean Society for Thoracic and Cardiovascular Surgery. All rights Reserved. This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jeon, Yeong Jeong
Son, Jongbae
Cho, Jong Ho
Harlequin Syndrome Following Resection of Mediastinal Ganglioneuroma
title Harlequin Syndrome Following Resection of Mediastinal Ganglioneuroma
title_full Harlequin Syndrome Following Resection of Mediastinal Ganglioneuroma
title_fullStr Harlequin Syndrome Following Resection of Mediastinal Ganglioneuroma
title_full_unstemmed Harlequin Syndrome Following Resection of Mediastinal Ganglioneuroma
title_short Harlequin Syndrome Following Resection of Mediastinal Ganglioneuroma
title_sort harlequin syndrome following resection of mediastinal ganglioneuroma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380209/
https://www.ncbi.nlm.nih.gov/pubmed/28382275
http://dx.doi.org/10.5090/kjtcs.2017.50.2.130
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