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Clinical characteristics of Epstein–Barr virus infection in the pediatric nervous system

BACKGROUND: To investigate the clinical characteristics of Epstein–Barr virus (EBV) infection in the pediatric nervous system (NS). METHODS: We retrospectively analyzed the clinical data and follow-up results of 89 children with neurological damage caused by EBV who were hospitalized in the children...

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Autores principales: Cheng, Huan, Chen, Doudou, Peng, Xiaoling, Wu, Peng, Jiang, Li, Hu, Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691062/
https://www.ncbi.nlm.nih.gov/pubmed/33238935
http://dx.doi.org/10.1186/s12879-020-05623-1
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author Cheng, Huan
Chen, Doudou
Peng, Xiaoling
Wu, Peng
Jiang, Li
Hu, Yue
author_facet Cheng, Huan
Chen, Doudou
Peng, Xiaoling
Wu, Peng
Jiang, Li
Hu, Yue
author_sort Cheng, Huan
collection PubMed
description BACKGROUND: To investigate the clinical characteristics of Epstein–Barr virus (EBV) infection in the pediatric nervous system (NS). METHODS: We retrospectively analyzed the clinical data and follow-up results of 89 children with neurological damage caused by EBV who were hospitalized in the children’s hospital of Chongqing Medical University from January 2008 to April 2019. RESULTS: EBV infection of the NS can occur at any time of the year. The highest incidence was seen in the age group of 0–4 years. Fever is the main clinical feature (74/89, 83.1%). The main clinical types were encephalitis/meningoencephalitis (64/89, 71.9%), acute myelitis (2/89, 2.2%), acute disseminated encephalomyelitis (ADEM) (3/89, 3.4%), Guillain–Barré Syndrome (GBS) (15/89, 16.9%), neurological damage caused by EBV-hemophagocytic lymphohistiocytosis (EBV-HLH) (4/89, 4.5%), and NS-post-transplant lymphoproliferative disorder (NS-PTLD) (1/89, 1.1%). Anti-N-methyl-D-aspartate receptor encephalitis was found during the convalescence of EBV encephalitis. EBV encephalitis/meningitis showed no symptoms of tonsillitis, lymph node enlargement, skin rash, hepatosplenomegaly. Acute motor axonal neuropathy is the chief complication in GBS caused by EBV. CONCLUSION: There were significant differences in neurological complications caused by EBV. The prognosis of EBV infection in the NS is generally good. These illnesses are often self-limiting. A few cases may show residual sequelae.
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spelling pubmed-76910622020-11-30 Clinical characteristics of Epstein–Barr virus infection in the pediatric nervous system Cheng, Huan Chen, Doudou Peng, Xiaoling Wu, Peng Jiang, Li Hu, Yue BMC Infect Dis Research Article BACKGROUND: To investigate the clinical characteristics of Epstein–Barr virus (EBV) infection in the pediatric nervous system (NS). METHODS: We retrospectively analyzed the clinical data and follow-up results of 89 children with neurological damage caused by EBV who were hospitalized in the children’s hospital of Chongqing Medical University from January 2008 to April 2019. RESULTS: EBV infection of the NS can occur at any time of the year. The highest incidence was seen in the age group of 0–4 years. Fever is the main clinical feature (74/89, 83.1%). The main clinical types were encephalitis/meningoencephalitis (64/89, 71.9%), acute myelitis (2/89, 2.2%), acute disseminated encephalomyelitis (ADEM) (3/89, 3.4%), Guillain–Barré Syndrome (GBS) (15/89, 16.9%), neurological damage caused by EBV-hemophagocytic lymphohistiocytosis (EBV-HLH) (4/89, 4.5%), and NS-post-transplant lymphoproliferative disorder (NS-PTLD) (1/89, 1.1%). Anti-N-methyl-D-aspartate receptor encephalitis was found during the convalescence of EBV encephalitis. EBV encephalitis/meningitis showed no symptoms of tonsillitis, lymph node enlargement, skin rash, hepatosplenomegaly. Acute motor axonal neuropathy is the chief complication in GBS caused by EBV. CONCLUSION: There were significant differences in neurological complications caused by EBV. The prognosis of EBV infection in the NS is generally good. These illnesses are often self-limiting. A few cases may show residual sequelae. BioMed Central 2020-11-25 /pmc/articles/PMC7691062/ /pubmed/33238935 http://dx.doi.org/10.1186/s12879-020-05623-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Cheng, Huan
Chen, Doudou
Peng, Xiaoling
Wu, Peng
Jiang, Li
Hu, Yue
Clinical characteristics of Epstein–Barr virus infection in the pediatric nervous system
title Clinical characteristics of Epstein–Barr virus infection in the pediatric nervous system
title_full Clinical characteristics of Epstein–Barr virus infection in the pediatric nervous system
title_fullStr Clinical characteristics of Epstein–Barr virus infection in the pediatric nervous system
title_full_unstemmed Clinical characteristics of Epstein–Barr virus infection in the pediatric nervous system
title_short Clinical characteristics of Epstein–Barr virus infection in the pediatric nervous system
title_sort clinical characteristics of epstein–barr virus infection in the pediatric nervous system
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691062/
https://www.ncbi.nlm.nih.gov/pubmed/33238935
http://dx.doi.org/10.1186/s12879-020-05623-1
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