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Reversible splenial lesion syndrome associated with encephalitis/encephalopathy presenting with great clinical heterogeneity
BACKGROUND: Reversible splenial lesion syndrome (RESLES) is a disorder radiologically characterized by reversible lesion in the splenium of the corpus callosum (SCC). Most of patients with RESLES associated with encephalitis/encephalopathy were identified in Japanese population, but almost no Chines...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835842/ https://www.ncbi.nlm.nih.gov/pubmed/27089920 http://dx.doi.org/10.1186/s12883-016-0572-9 |
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author | Zhu, Yuanzhao Zheng, Junjun Zhang, Ling Zeng, Zhenguo Zhu, Min Li, Xiaobin Lou, Xiaoliang Wan, Hui Hong, Daojun |
author_facet | Zhu, Yuanzhao Zheng, Junjun Zhang, Ling Zeng, Zhenguo Zhu, Min Li, Xiaobin Lou, Xiaoliang Wan, Hui Hong, Daojun |
author_sort | Zhu, Yuanzhao |
collection | PubMed |
description | BACKGROUND: Reversible splenial lesion syndrome (RESLES) is a disorder radiologically characterized by reversible lesion in the splenium of the corpus callosum (SCC). Most of patients with RESLES associated with encephalitis/encephalopathy were identified in Japanese population, but almost no Chinese patients were diagnosed as RESLES associated with encephalitis/encephalopathy. METHODS: Possible patients with reversible isolated SCC lesions were retrieved from January 2012 to July 2015 using keyword “restricted diffusion and isolated SCC lesion” in MRI report system from a large academic center. The clinical, laboratory and radiological data were summarized. RESULTS: A total of 15 encephalitis/encephalopathy patients (9 males and 6 females) were identified with a reversible isolated SCC lesion. Except for 13 patients with fever symptom, 8 patients also had cold symptoms before the onset of neurological symptoms. The neurological symptoms included headache, vertigo, seizure, disturbance of consciousness, and delirious behavior. Thirteen patients completely recovered within 1 month, but 2 patients who were subjected to mechanical ventilation had persistent neurological deficits. The initial MRI features showed isolated ovoid or extending SCC lesions with homogeneous hyperintense on diffusion weighted imaging (DWI) and decreased apparent diffusion coefficient (ADC) values. The follow-up MRI revealed that isolated SCC lesions with diffuse restriction disappeared at 10 to 32 days after the initial MRI study. Fractional anisotropy map revealed the decreased value of SCC lesion in a severe case with poor prognosis. CONCLUSIONS: RESLES associated with encephalitis/encephalopathy is a reversible syndrome with an excellent prognosis in most patients, while a few patients required ventilator supporting at the early stage might have severe neurological sequelae. Reversible signal changes on DWI and ADC are identified in all patients, but fractional anisotropy values can be decreased in severe patient with neurological sequelae. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12883-016-0572-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4835842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48358422016-04-20 Reversible splenial lesion syndrome associated with encephalitis/encephalopathy presenting with great clinical heterogeneity Zhu, Yuanzhao Zheng, Junjun Zhang, Ling Zeng, Zhenguo Zhu, Min Li, Xiaobin Lou, Xiaoliang Wan, Hui Hong, Daojun BMC Neurol Research Article BACKGROUND: Reversible splenial lesion syndrome (RESLES) is a disorder radiologically characterized by reversible lesion in the splenium of the corpus callosum (SCC). Most of patients with RESLES associated with encephalitis/encephalopathy were identified in Japanese population, but almost no Chinese patients were diagnosed as RESLES associated with encephalitis/encephalopathy. METHODS: Possible patients with reversible isolated SCC lesions were retrieved from January 2012 to July 2015 using keyword “restricted diffusion and isolated SCC lesion” in MRI report system from a large academic center. The clinical, laboratory and radiological data were summarized. RESULTS: A total of 15 encephalitis/encephalopathy patients (9 males and 6 females) were identified with a reversible isolated SCC lesion. Except for 13 patients with fever symptom, 8 patients also had cold symptoms before the onset of neurological symptoms. The neurological symptoms included headache, vertigo, seizure, disturbance of consciousness, and delirious behavior. Thirteen patients completely recovered within 1 month, but 2 patients who were subjected to mechanical ventilation had persistent neurological deficits. The initial MRI features showed isolated ovoid or extending SCC lesions with homogeneous hyperintense on diffusion weighted imaging (DWI) and decreased apparent diffusion coefficient (ADC) values. The follow-up MRI revealed that isolated SCC lesions with diffuse restriction disappeared at 10 to 32 days after the initial MRI study. Fractional anisotropy map revealed the decreased value of SCC lesion in a severe case with poor prognosis. CONCLUSIONS: RESLES associated with encephalitis/encephalopathy is a reversible syndrome with an excellent prognosis in most patients, while a few patients required ventilator supporting at the early stage might have severe neurological sequelae. Reversible signal changes on DWI and ADC are identified in all patients, but fractional anisotropy values can be decreased in severe patient with neurological sequelae. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12883-016-0572-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-18 /pmc/articles/PMC4835842/ /pubmed/27089920 http://dx.doi.org/10.1186/s12883-016-0572-9 Text en © Zhu et al. 2016 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 | Research Article Zhu, Yuanzhao Zheng, Junjun Zhang, Ling Zeng, Zhenguo Zhu, Min Li, Xiaobin Lou, Xiaoliang Wan, Hui Hong, Daojun Reversible splenial lesion syndrome associated with encephalitis/encephalopathy presenting with great clinical heterogeneity |
title | Reversible splenial lesion syndrome associated with encephalitis/encephalopathy presenting with great clinical heterogeneity |
title_full | Reversible splenial lesion syndrome associated with encephalitis/encephalopathy presenting with great clinical heterogeneity |
title_fullStr | Reversible splenial lesion syndrome associated with encephalitis/encephalopathy presenting with great clinical heterogeneity |
title_full_unstemmed | Reversible splenial lesion syndrome associated with encephalitis/encephalopathy presenting with great clinical heterogeneity |
title_short | Reversible splenial lesion syndrome associated with encephalitis/encephalopathy presenting with great clinical heterogeneity |
title_sort | reversible splenial lesion syndrome associated with encephalitis/encephalopathy presenting with great clinical heterogeneity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835842/ https://www.ncbi.nlm.nih.gov/pubmed/27089920 http://dx.doi.org/10.1186/s12883-016-0572-9 |
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