Rotavirus-associated mild encephalopathy with a reversible splenial lesion (MERS)—case report and review of the literature

BMC Infectious Diseases

Case Report

Ian R. Morrison¹  Christina Spyridou¹  Andrew J. Prendergast²  Konstantinos Karampatsas³  Cheuk Y. W. Tong⁴ 

[1] Department of Paediatrics, The Royal London Hospital, Barts Health NHS Trust, London, UK;Department of Paediatrics, The Royal London Hospital, Barts Health NHS Trust, London, UK;Centre for Paediatrics, Blizard Institute, Queen Mary University of London, London, UK;Department of Paediatrics, The Royal London Hospital, Barts Health NHS Trust, London, UK;Queen’s Hospital, Barking, Havering and Redbridge University Hospitals NHS Trust, Romford, UK;Department of Virology, The Royal London Hospital, Barts Health NHS Trust, London, UK;

关键词: Rotavirus;    Encephalopathy;    Central Nervous System Infection;    Corpus Callosum;    MERS;    Paediatrics;   

DOI  :  10.1186/s12879-015-1192-5

 received in 2015-05-06, accepted in 2015-10-07,  发布年份 2015

来源: Springer

【 摘 要 】

BackgroundRotavirus 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 presentationA 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.ConclusionMERS 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.

【 授权许可】

CC BY   
© Karampatsas et al. 2015