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A case of reversible splenial lesion syndrome secondary to Fanconi syndrome with white matter swelling as the main manifestation
Reversible splenial lesion syndrome (RESLES) is a rare clinical imaging syndrome that is characterized by magnetic resonance imaging (MRI) findings of reversible abnormal signals in the splenium of the corpus callosum (SCC). There are a variety of pathogenic causes, including infection, metabolic di...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838877/ https://www.ncbi.nlm.nih.gov/pubmed/33472487 http://dx.doi.org/10.1177/0300060520985713 |
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author | Han, Jingzhe Wang, Yaye Wu, Yue Zhang, Jinru Song, Xueqin Ji, Guang |
author_facet | Han, Jingzhe Wang, Yaye Wu, Yue Zhang, Jinru Song, Xueqin Ji, Guang |
author_sort | Han, Jingzhe |
collection | PubMed |
description | Reversible splenial lesion syndrome (RESLES) is a rare clinical imaging syndrome that is characterized by magnetic resonance imaging (MRI) findings of reversible abnormal signals in the splenium of the corpus callosum (SCC). There are a variety of pathogenic causes, including infection, metabolic disturbances, and antiepileptic drug use. Moreover, the disease is clinically rare and easily misdiagnosed. Here, we report a unique case of a 32-year-old man with Fanconi syndrome who had an intensified signal in the SCC and diffuse white matter swelling on MRI. We believe this to be the first adult case of RESLES as a manifestation of Fanconi syndrome, which further expands the disease spectrum leading to RESLES. The imaging features of this case included extensive lesions, symmetrical diffuse restricted signals, and reversibility. The identification of these features improves our understanding of the imaging characteristics of RESLES, thus enabling clinicians to better understand this disease, correctly establish its diagnosis, and improve its prognosis in this kind of patient. |
format | Online Article Text |
id | pubmed-7838877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-78388772021-02-05 A case of reversible splenial lesion syndrome secondary to Fanconi syndrome with white matter swelling as the main manifestation Han, Jingzhe Wang, Yaye Wu, Yue Zhang, Jinru Song, Xueqin Ji, Guang J Int Med Res Case Report Reversible splenial lesion syndrome (RESLES) is a rare clinical imaging syndrome that is characterized by magnetic resonance imaging (MRI) findings of reversible abnormal signals in the splenium of the corpus callosum (SCC). There are a variety of pathogenic causes, including infection, metabolic disturbances, and antiepileptic drug use. Moreover, the disease is clinically rare and easily misdiagnosed. Here, we report a unique case of a 32-year-old man with Fanconi syndrome who had an intensified signal in the SCC and diffuse white matter swelling on MRI. We believe this to be the first adult case of RESLES as a manifestation of Fanconi syndrome, which further expands the disease spectrum leading to RESLES. The imaging features of this case included extensive lesions, symmetrical diffuse restricted signals, and reversibility. The identification of these features improves our understanding of the imaging characteristics of RESLES, thus enabling clinicians to better understand this disease, correctly establish its diagnosis, and improve its prognosis in this kind of patient. SAGE Publications 2021-01-20 /pmc/articles/PMC7838877/ /pubmed/33472487 http://dx.doi.org/10.1177/0300060520985713 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report Han, Jingzhe Wang, Yaye Wu, Yue Zhang, Jinru Song, Xueqin Ji, Guang A case of reversible splenial lesion syndrome secondary to Fanconi syndrome with white matter swelling as the main manifestation |
title | A case of reversible splenial lesion syndrome secondary to Fanconi syndrome
with white matter swelling as the main manifestation |
title_full | A case of reversible splenial lesion syndrome secondary to Fanconi syndrome
with white matter swelling as the main manifestation |
title_fullStr | A case of reversible splenial lesion syndrome secondary to Fanconi syndrome
with white matter swelling as the main manifestation |
title_full_unstemmed | A case of reversible splenial lesion syndrome secondary to Fanconi syndrome
with white matter swelling as the main manifestation |
title_short | A case of reversible splenial lesion syndrome secondary to Fanconi syndrome
with white matter swelling as the main manifestation |
title_sort | case of reversible splenial lesion syndrome secondary to fanconi syndrome
with white matter swelling as the main manifestation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838877/ https://www.ncbi.nlm.nih.gov/pubmed/33472487 http://dx.doi.org/10.1177/0300060520985713 |
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