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Wallenberg's Syndrome: An Unusual Case of Dysphagia

A 56-year-old man presented with sudden-onset oropharyngeal dysphagia and vomiting of central etiology. Neurological evaluation showed uvula deviation to the left, paresis of the mid-right portion of the soft palate, lateralization of gaze to the right side, and dysphonia. Magnetic resonance imaging...

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Detalles Bibliográficos
Autores principales: Castillo, Aurora Loaeza-del, Barahona-Garrido, Josué, Criales, Sergio, Chang-Menéndez, Sergio, Torre, Aldo
Formato: Texto
Lenguaje:English
Publicado: S. Karger AG 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3073801/
https://www.ncbi.nlm.nih.gov/pubmed/21487559
http://dx.doi.org/10.1159/000110871
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author Castillo, Aurora Loaeza-del
Barahona-Garrido, Josué
Criales, Sergio
Chang-Menéndez, Sergio
Torre, Aldo
author_facet Castillo, Aurora Loaeza-del
Barahona-Garrido, Josué
Criales, Sergio
Chang-Menéndez, Sergio
Torre, Aldo
author_sort Castillo, Aurora Loaeza-del
collection PubMed
description A 56-year-old man presented with sudden-onset oropharyngeal dysphagia and vomiting of central etiology. Neurological evaluation showed uvula deviation to the left, paresis of the mid-right portion of the soft palate, lateralization of gaze to the right side, and dysphonia. Magnetic resonance imaging (MRI) showed an infarction in the left lateral medullary region, therefore the diagnosis of Wallenberg's syndrome was established. The neurological issues along with the dysphagia gradually improved and the patient was discharged.
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spelling pubmed-30738012011-04-12 Wallenberg's Syndrome: An Unusual Case of Dysphagia Castillo, Aurora Loaeza-del Barahona-Garrido, Josué Criales, Sergio Chang-Menéndez, Sergio Torre, Aldo Case Rep Gastroenterol Published: November 2007 A 56-year-old man presented with sudden-onset oropharyngeal dysphagia and vomiting of central etiology. Neurological evaluation showed uvula deviation to the left, paresis of the mid-right portion of the soft palate, lateralization of gaze to the right side, and dysphonia. Magnetic resonance imaging (MRI) showed an infarction in the left lateral medullary region, therefore the diagnosis of Wallenberg's syndrome was established. The neurological issues along with the dysphagia gradually improved and the patient was discharged. S. Karger AG 2007-11-09 /pmc/articles/PMC3073801/ /pubmed/21487559 http://dx.doi.org/10.1159/000110871 Text en Copyright © 2007 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No-Derivative-Works License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Published: November 2007
Castillo, Aurora Loaeza-del
Barahona-Garrido, Josué
Criales, Sergio
Chang-Menéndez, Sergio
Torre, Aldo
Wallenberg's Syndrome: An Unusual Case of Dysphagia
title Wallenberg's Syndrome: An Unusual Case of Dysphagia
title_full Wallenberg's Syndrome: An Unusual Case of Dysphagia
title_fullStr Wallenberg's Syndrome: An Unusual Case of Dysphagia
title_full_unstemmed Wallenberg's Syndrome: An Unusual Case of Dysphagia
title_short Wallenberg's Syndrome: An Unusual Case of Dysphagia
title_sort wallenberg's syndrome: an unusual case of dysphagia
topic Published: November 2007
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3073801/
https://www.ncbi.nlm.nih.gov/pubmed/21487559
http://dx.doi.org/10.1159/000110871
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