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Reversible splenial lesion syndrome in sisters with sensorineural deafness as the first manifestation

Reversible splenial lesion syndrome (RESLES) is a rare clinico-radiological disorder syndrome with unclear pathophysiology. Here, two sisters with sensorineural deafness as the chief complaint diagnosed with RESLES was reported. Although the sisters had the disease successively, they were divided in...

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Autores principales: Yang, Jinbo, Ma, Xiaodan, Li, Rujuan, Ma, Xiaohui, Chen, Junmin, Zhang, Xiangjian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170165/
https://www.ncbi.nlm.nih.gov/pubmed/34113728
http://dx.doi.org/10.1016/j.heliyon.2021.e07057
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author Yang, Jinbo
Ma, Xiaodan
Li, Rujuan
Ma, Xiaohui
Chen, Junmin
Zhang, Xiangjian
author_facet Yang, Jinbo
Ma, Xiaodan
Li, Rujuan
Ma, Xiaohui
Chen, Junmin
Zhang, Xiangjian
author_sort Yang, Jinbo
collection PubMed
description Reversible splenial lesion syndrome (RESLES) is a rare clinico-radiological disorder syndrome with unclear pathophysiology. Here, two sisters with sensorineural deafness as the chief complaint diagnosed with RESLES was reported. Although the sisters had the disease successively, they were divided into two types on imaging by isolated lesions of splenium of the corpus callosum (SCC) and extensive lesions of the corpus callosum. The clinical manifestations and lesions on MRI disappeared after 6 months. The sensorineural deafness of the sisters in this article may be caused by transcallosal auditory pathway (TCAP) injury. Auditory handicap has been found in previous RESLES cases, indicating that we know little about the connection between the SCC and the auditory pathway, and further research is needed.
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spelling pubmed-81701652021-06-09 Reversible splenial lesion syndrome in sisters with sensorineural deafness as the first manifestation Yang, Jinbo Ma, Xiaodan Li, Rujuan Ma, Xiaohui Chen, Junmin Zhang, Xiangjian Heliyon Case Report Reversible splenial lesion syndrome (RESLES) is a rare clinico-radiological disorder syndrome with unclear pathophysiology. Here, two sisters with sensorineural deafness as the chief complaint diagnosed with RESLES was reported. Although the sisters had the disease successively, they were divided into two types on imaging by isolated lesions of splenium of the corpus callosum (SCC) and extensive lesions of the corpus callosum. The clinical manifestations and lesions on MRI disappeared after 6 months. The sensorineural deafness of the sisters in this article may be caused by transcallosal auditory pathway (TCAP) injury. Auditory handicap has been found in previous RESLES cases, indicating that we know little about the connection between the SCC and the auditory pathway, and further research is needed. Elsevier 2021-05-26 /pmc/articles/PMC8170165/ /pubmed/34113728 http://dx.doi.org/10.1016/j.heliyon.2021.e07057 Text en © 2021 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Yang, Jinbo
Ma, Xiaodan
Li, Rujuan
Ma, Xiaohui
Chen, Junmin
Zhang, Xiangjian
Reversible splenial lesion syndrome in sisters with sensorineural deafness as the first manifestation
title Reversible splenial lesion syndrome in sisters with sensorineural deafness as the first manifestation
title_full Reversible splenial lesion syndrome in sisters with sensorineural deafness as the first manifestation
title_fullStr Reversible splenial lesion syndrome in sisters with sensorineural deafness as the first manifestation
title_full_unstemmed Reversible splenial lesion syndrome in sisters with sensorineural deafness as the first manifestation
title_short Reversible splenial lesion syndrome in sisters with sensorineural deafness as the first manifestation
title_sort reversible splenial lesion syndrome in sisters with sensorineural deafness as the first manifestation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170165/
https://www.ncbi.nlm.nih.gov/pubmed/34113728
http://dx.doi.org/10.1016/j.heliyon.2021.e07057
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