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Rotavirus-associated mild encephalopathy with a reversible splenial lesion (MERS)—case report and review of the literature
BACKGROUND: Rotavirus is the most common cause of severe gastroenteritis in children under the age of 5 years worldwide. It is well recognised that rotavirus can cause signs and symptoms beyond the gastrointestinal tract, including neurological manifestations such as encephalopathy. Mild encephalopa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619335/ https://www.ncbi.nlm.nih.gov/pubmed/26499987 http://dx.doi.org/10.1186/s12879-015-1192-5 |
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author | Karampatsas, Konstantinos Spyridou, Christina Morrison, Ian R. Tong, Cheuk Y. W. Prendergast, Andrew J. |
author_facet | Karampatsas, Konstantinos Spyridou, Christina Morrison, Ian R. Tong, Cheuk Y. W. Prendergast, Andrew J. |
author_sort | Karampatsas, Konstantinos |
collection | PubMed |
description | BACKGROUND: Rotavirus is the most common cause of severe gastroenteritis in children under the age of 5 years worldwide. It is well recognised that rotavirus can cause signs and symptoms beyond the gastrointestinal tract, including neurological manifestations such as encephalopathy. Mild encephalopathy with a reversible splenial lesion (MERS) is a clinico-radiological syndrome that has been associated with rotavirus. We report a case of a 4-year-old boy with clinically mild encephalopathy, who had an isolated splenial lesion in the corpus callosum on neuroimaging, and rotavirus RNA detected in faeces. We use this case as an opportunity to review the literature on rotavirus-associated MERS. CASE PRESENTATION: A previously healthy 4-year-old boy presented with a 2-day history of vomiting, diarrhoea, and fever, complicated by reduced level of consciousness. Magnetic resonance imaging of the brain showed a marked hyperintensity in the splenium of the corpus callosum on T2 and diffusion-weighted images. Rotavirus genome was detected by polymerase chain reaction in a stool specimen, but not in the cerebrospinal fluid. The genotype was identified as G1P8. His clinical condition improved with gradual resolution of his symptoms. No neurological complications were evident upon discharge and the patient had no recurring symptoms or significant residual defects when followed up 2 months later. CONCLUSION: MERS is a novel clinic-radiological syndrome first described in Japan. A transient splenial lesion with reduced diffusion that appears as a high signal intensity in diffusion-weighted MRI is the main diagnostic feature. Rotavirus is one of the most common agents associated with MERS, although to our knowledge only one previous case has been reported from Europe. The majority of patients appear to achieve full recovery following rotavirus-associated MERS, irrespective of treatment. This case, together with other published reports, supports the hypothesis that rotavirus-associated MERS is unlikely to be the result of direct viral invasion of the CNS. It has been suggested that MERS may be caused by intra-myelinic axonal oedema or local inflammatory cell infiltration; however, the pathogenesis remains incompletely understood. |
format | Online Article Text |
id | pubmed-4619335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46193352015-10-26 Rotavirus-associated mild encephalopathy with a reversible splenial lesion (MERS)—case report and review of the literature Karampatsas, Konstantinos Spyridou, Christina Morrison, Ian R. Tong, Cheuk Y. W. Prendergast, Andrew J. BMC Infect Dis Case Report BACKGROUND: Rotavirus is the most common cause of severe gastroenteritis in children under the age of 5 years worldwide. It is well recognised that rotavirus can cause signs and symptoms beyond the gastrointestinal tract, including neurological manifestations such as encephalopathy. Mild encephalopathy with a reversible splenial lesion (MERS) is a clinico-radiological syndrome that has been associated with rotavirus. We report a case of a 4-year-old boy with clinically mild encephalopathy, who had an isolated splenial lesion in the corpus callosum on neuroimaging, and rotavirus RNA detected in faeces. We use this case as an opportunity to review the literature on rotavirus-associated MERS. CASE PRESENTATION: A previously healthy 4-year-old boy presented with a 2-day history of vomiting, diarrhoea, and fever, complicated by reduced level of consciousness. Magnetic resonance imaging of the brain showed a marked hyperintensity in the splenium of the corpus callosum on T2 and diffusion-weighted images. Rotavirus genome was detected by polymerase chain reaction in a stool specimen, but not in the cerebrospinal fluid. The genotype was identified as G1P8. His clinical condition improved with gradual resolution of his symptoms. No neurological complications were evident upon discharge and the patient had no recurring symptoms or significant residual defects when followed up 2 months later. CONCLUSION: MERS is a novel clinic-radiological syndrome first described in Japan. A transient splenial lesion with reduced diffusion that appears as a high signal intensity in diffusion-weighted MRI is the main diagnostic feature. Rotavirus is one of the most common agents associated with MERS, although to our knowledge only one previous case has been reported from Europe. The majority of patients appear to achieve full recovery following rotavirus-associated MERS, irrespective of treatment. This case, together with other published reports, supports the hypothesis that rotavirus-associated MERS is unlikely to be the result of direct viral invasion of the CNS. It has been suggested that MERS may be caused by intra-myelinic axonal oedema or local inflammatory cell infiltration; however, the pathogenesis remains incompletely understood. BioMed Central 2015-10-24 /pmc/articles/PMC4619335/ /pubmed/26499987 http://dx.doi.org/10.1186/s12879-015-1192-5 Text en © Karampatsas et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Case Report Karampatsas, Konstantinos Spyridou, Christina Morrison, Ian R. Tong, Cheuk Y. W. Prendergast, Andrew J. Rotavirus-associated mild encephalopathy with a reversible splenial lesion (MERS)—case report and review of the literature |
title | Rotavirus-associated mild encephalopathy with a reversible splenial lesion (MERS)—case report and review of the literature |
title_full | Rotavirus-associated mild encephalopathy with a reversible splenial lesion (MERS)—case report and review of the literature |
title_fullStr | Rotavirus-associated mild encephalopathy with a reversible splenial lesion (MERS)—case report and review of the literature |
title_full_unstemmed | Rotavirus-associated mild encephalopathy with a reversible splenial lesion (MERS)—case report and review of the literature |
title_short | Rotavirus-associated mild encephalopathy with a reversible splenial lesion (MERS)—case report and review of the literature |
title_sort | rotavirus-associated mild encephalopathy with a reversible splenial lesion (mers)—case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619335/ https://www.ncbi.nlm.nih.gov/pubmed/26499987 http://dx.doi.org/10.1186/s12879-015-1192-5 |
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