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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Thoracic and Cardiovascular Surgery
2017
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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. |
format | Online Article Text |
id | pubmed-5380209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Korean Society for Thoracic and Cardiovascular Surgery |
record_format | MEDLINE/PubMed |
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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