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Clinical analysis of reversible splenial lesion syndrome in Chinese adults: A retrospective study of 11 cases

Reversible splenial lesion syndrome (RESLES) is a clinico-radiological entity that defines a reversible lesion in the splenium of the corpus callosum (SCC) on magnetic resonance imaging (MRI). The clinical and radiological characteristics of RESLES are poorly defined and most RESLES literature is in...

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Autores principales: Gao, Xiaoyu, Feng, Qiaochan, Arif, Saeed, Liaqat, Jahanzeb, Li, Bing, Jiang, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478579/
https://www.ncbi.nlm.nih.gov/pubmed/32899066
http://dx.doi.org/10.1097/MD.0000000000022052
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author Gao, Xiaoyu
Feng, Qiaochan
Arif, Saeed
Liaqat, Jahanzeb
Li, Bing
Jiang, Kun
author_facet Gao, Xiaoyu
Feng, Qiaochan
Arif, Saeed
Liaqat, Jahanzeb
Li, Bing
Jiang, Kun
author_sort Gao, Xiaoyu
collection PubMed
description Reversible splenial lesion syndrome (RESLES) is a clinico-radiological entity that defines a reversible lesion in the splenium of the corpus callosum (SCC) on magnetic resonance imaging (MRI). The clinical and radiological characteristics of RESLES are poorly defined and most RESLES literature is in the form of case reports. We reviewed the clinical and radiological data from 11 RESLES patients in order to more clearly describe the characteristics of this disorder in adults. Patients included in this study were diagnosed with RESLES from May 2012 to March 2018. We collected clinical, imaging, and laboratory data of 11 adult patients from Neurology Department of the Affliated Yantai Yuhuangding Hospital of Qingdao University. After analyzing various clinico-radiological features and laboratory parameters, including serum sodium, pathogen testing, cerebrospinal fluid (CSF) studies, electroencephalography (EEG), and MRI findings, we made a diagnosis of RESLES based on the criteria proposed previously by Garcia-Monco et al. Of the 11 patients, 7 (63.63%) were male and 4 (36.36%) were female, ranging in age from 24 to 62 years with an average age of 31.48 ± 11.47 years. Seven cases occurred in the months of winter and spring (December–March). The primary clinical symptoms were headache, seizure, disturbance of consciousness, mental abnormality, and dizziness. All 11 patients had lesions in the SCC and all the lesions disappeared or significantly improved on follow-up imaging that was done within a month of symptom resolution. We found 5 (45.45%) patients had a CSF opening pressure >180 mmH(2)O, in addition to elevated protein and(or) leukocytes levels in 3 (27.27%) patients. The serum sodium concentration in 6 (54.55%) patients was low (<137 mmol/L) and EEG showed nonspecific slowing in waves 4 (36.36%) patients. When we encounter clinical manifestations such as headache accompanied with mental symptoms, disturbance of consciousness or epilepsy, and brain MRI finds lesions of the corpus callosum, we should consider whether it is RESLES. In order to find out the possible cause of the disease, we should carefully inquire about the history of the disease, complete etiology examination, and CSF tests. Of course, it is one of the necessary conditions for the diagnosis that the lesions in the corpus callosum are obviously relieved or disappeared.
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spelling pubmed-74785792020-09-24 Clinical analysis of reversible splenial lesion syndrome in Chinese adults: A retrospective study of 11 cases Gao, Xiaoyu Feng, Qiaochan Arif, Saeed Liaqat, Jahanzeb Li, Bing Jiang, Kun Medicine (Baltimore) 5300 Reversible splenial lesion syndrome (RESLES) is a clinico-radiological entity that defines a reversible lesion in the splenium of the corpus callosum (SCC) on magnetic resonance imaging (MRI). The clinical and radiological characteristics of RESLES are poorly defined and most RESLES literature is in the form of case reports. We reviewed the clinical and radiological data from 11 RESLES patients in order to more clearly describe the characteristics of this disorder in adults. Patients included in this study were diagnosed with RESLES from May 2012 to March 2018. We collected clinical, imaging, and laboratory data of 11 adult patients from Neurology Department of the Affliated Yantai Yuhuangding Hospital of Qingdao University. After analyzing various clinico-radiological features and laboratory parameters, including serum sodium, pathogen testing, cerebrospinal fluid (CSF) studies, electroencephalography (EEG), and MRI findings, we made a diagnosis of RESLES based on the criteria proposed previously by Garcia-Monco et al. Of the 11 patients, 7 (63.63%) were male and 4 (36.36%) were female, ranging in age from 24 to 62 years with an average age of 31.48 ± 11.47 years. Seven cases occurred in the months of winter and spring (December–March). The primary clinical symptoms were headache, seizure, disturbance of consciousness, mental abnormality, and dizziness. All 11 patients had lesions in the SCC and all the lesions disappeared or significantly improved on follow-up imaging that was done within a month of symptom resolution. We found 5 (45.45%) patients had a CSF opening pressure >180 mmH(2)O, in addition to elevated protein and(or) leukocytes levels in 3 (27.27%) patients. The serum sodium concentration in 6 (54.55%) patients was low (<137 mmol/L) and EEG showed nonspecific slowing in waves 4 (36.36%) patients. When we encounter clinical manifestations such as headache accompanied with mental symptoms, disturbance of consciousness or epilepsy, and brain MRI finds lesions of the corpus callosum, we should consider whether it is RESLES. In order to find out the possible cause of the disease, we should carefully inquire about the history of the disease, complete etiology examination, and CSF tests. Of course, it is one of the necessary conditions for the diagnosis that the lesions in the corpus callosum are obviously relieved or disappeared. Lippincott Williams & Wilkins 2020-09-04 /pmc/articles/PMC7478579/ /pubmed/32899066 http://dx.doi.org/10.1097/MD.0000000000022052 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 5300
Gao, Xiaoyu
Feng, Qiaochan
Arif, Saeed
Liaqat, Jahanzeb
Li, Bing
Jiang, Kun
Clinical analysis of reversible splenial lesion syndrome in Chinese adults: A retrospective study of 11 cases
title Clinical analysis of reversible splenial lesion syndrome in Chinese adults: A retrospective study of 11 cases
title_full Clinical analysis of reversible splenial lesion syndrome in Chinese adults: A retrospective study of 11 cases
title_fullStr Clinical analysis of reversible splenial lesion syndrome in Chinese adults: A retrospective study of 11 cases
title_full_unstemmed Clinical analysis of reversible splenial lesion syndrome in Chinese adults: A retrospective study of 11 cases
title_short Clinical analysis of reversible splenial lesion syndrome in Chinese adults: A retrospective study of 11 cases
title_sort clinical analysis of reversible splenial lesion syndrome in chinese adults: a retrospective study of 11 cases
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478579/
https://www.ncbi.nlm.nih.gov/pubmed/32899066
http://dx.doi.org/10.1097/MD.0000000000022052
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