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Wernicke's encephalopathy in a child with high dose thiamine therapy

Wernicke's encephalopathy is an acute neurological disorder characterized by mental confusion, oculomotor dysfunction, and ataxia. It has been reported in individuals with alcohol dependence, hyperemesis gravidarum, and prolonged parenteral nutrition without vitamin supplementation. Here we pre...

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Autores principales: Park, So Won, Yi, Yoon Young, Han, Jung Woo, Kim, Heung Dong, Lee, Joon Soo, Kang, Hoon-Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279011/
https://www.ncbi.nlm.nih.gov/pubmed/25550705
http://dx.doi.org/10.3345/kjp.2014.57.11.496
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author Park, So Won
Yi, Yoon Young
Han, Jung Woo
Kim, Heung Dong
Lee, Joon Soo
Kang, Hoon-Chul
author_facet Park, So Won
Yi, Yoon Young
Han, Jung Woo
Kim, Heung Dong
Lee, Joon Soo
Kang, Hoon-Chul
author_sort Park, So Won
collection PubMed
description Wernicke's encephalopathy is an acute neurological disorder characterized by mental confusion, oculomotor dysfunction, and ataxia. It has been reported in individuals with alcohol dependence, hyperemesis gravidarum, and prolonged parenteral nutrition without vitamin supplementation. Here we present the case of a 13-year-old male patient with neuroblastoma and a history of poor oral intake and nausea for 3 months. After admission, he showed gait disturbances, nystagmus, and excessive dizziness; his mental state, however, indicated he was alert, which did not fit the classical triad of Wernicke's encephalopathy. A diagnosis of Wernicke's encephalopathy was made only after brain magnetic resonance imaging and serum thiamine level analyses were performed. The patient's symptoms remained after 5 days of treatment with 100-mg thiamine once daily; thus, we increased the dosage to 500 mg 3 times daily, 1,500 mg per day. His symptoms then improved after 20 days of replacement therapy. This case report describes a pediatric patient who was promptly diagnosed with Wernicke's encephalopathy, despite only 2 suspicious symptoms, and who completely recovered after high doses of thiamine were given intravenously.
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spelling pubmed-42790112014-12-30 Wernicke's encephalopathy in a child with high dose thiamine therapy Park, So Won Yi, Yoon Young Han, Jung Woo Kim, Heung Dong Lee, Joon Soo Kang, Hoon-Chul Korean J Pediatr Case Report Wernicke's encephalopathy is an acute neurological disorder characterized by mental confusion, oculomotor dysfunction, and ataxia. It has been reported in individuals with alcohol dependence, hyperemesis gravidarum, and prolonged parenteral nutrition without vitamin supplementation. Here we present the case of a 13-year-old male patient with neuroblastoma and a history of poor oral intake and nausea for 3 months. After admission, he showed gait disturbances, nystagmus, and excessive dizziness; his mental state, however, indicated he was alert, which did not fit the classical triad of Wernicke's encephalopathy. A diagnosis of Wernicke's encephalopathy was made only after brain magnetic resonance imaging and serum thiamine level analyses were performed. The patient's symptoms remained after 5 days of treatment with 100-mg thiamine once daily; thus, we increased the dosage to 500 mg 3 times daily, 1,500 mg per day. His symptoms then improved after 20 days of replacement therapy. This case report describes a pediatric patient who was promptly diagnosed with Wernicke's encephalopathy, despite only 2 suspicious symptoms, and who completely recovered after high doses of thiamine were given intravenously. The Korean Pediatric Society 2014-11 2014-11-30 /pmc/articles/PMC4279011/ /pubmed/25550705 http://dx.doi.org/10.3345/kjp.2014.57.11.496 Text en Copyright © 2014 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Park, So Won
Yi, Yoon Young
Han, Jung Woo
Kim, Heung Dong
Lee, Joon Soo
Kang, Hoon-Chul
Wernicke's encephalopathy in a child with high dose thiamine therapy
title Wernicke's encephalopathy in a child with high dose thiamine therapy
title_full Wernicke's encephalopathy in a child with high dose thiamine therapy
title_fullStr Wernicke's encephalopathy in a child with high dose thiamine therapy
title_full_unstemmed Wernicke's encephalopathy in a child with high dose thiamine therapy
title_short Wernicke's encephalopathy in a child with high dose thiamine therapy
title_sort wernicke's encephalopathy in a child with high dose thiamine therapy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279011/
https://www.ncbi.nlm.nih.gov/pubmed/25550705
http://dx.doi.org/10.3345/kjp.2014.57.11.496
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