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Cerebellar Degeneration Associated with Sjögren's Syndrome
BACKGROUND: Neurologic manifestations of primary Sjögren's syndrome (PSS) have been reported to vary from sensory polyneuropathy to encephalopathy or psychiatric problems. However, marked cerebellar degeneration associated with PSS has rarely been reported. CASE REPORT: We describe a patient wi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neurological Association
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391622/ https://www.ncbi.nlm.nih.gov/pubmed/22787501 http://dx.doi.org/10.3988/jcn.2012.8.2.155 |
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author | Kim, Mi Jung Lee, Myoung Chong Lee, Jae-Hong Chung, Sun Ju |
author_facet | Kim, Mi Jung Lee, Myoung Chong Lee, Jae-Hong Chung, Sun Ju |
author_sort | Kim, Mi Jung |
collection | PubMed |
description | BACKGROUND: Neurologic manifestations of primary Sjögren's syndrome (PSS) have been reported to vary from sensory polyneuropathy to encephalopathy or psychiatric problems. However, marked cerebellar degeneration associated with PSS has rarely been reported. CASE REPORT: We describe a patient with Sjögren's syndrome who exhibited rapidly progressive cerebellar ataxia, nystagmus, cognitive decline, and psychiatric problems. Brain magnetic resonance imaging revealed marked atrophy of the cerebellum, and (18)F-fluorodeoxyglucose positron-emission tomography demonstrated glucose hypometabolism of the cerebellum. CONCLUSIONS: Our PSS patient exhibited a progressive course of cerebellar syndrome, as evidenced by cerebellar atrophy on serial brain images. |
format | Online Article Text |
id | pubmed-3391622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Korean Neurological Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-33916222012-07-11 Cerebellar Degeneration Associated with Sjögren's Syndrome Kim, Mi Jung Lee, Myoung Chong Lee, Jae-Hong Chung, Sun Ju J Clin Neurol Case Report BACKGROUND: Neurologic manifestations of primary Sjögren's syndrome (PSS) have been reported to vary from sensory polyneuropathy to encephalopathy or psychiatric problems. However, marked cerebellar degeneration associated with PSS has rarely been reported. CASE REPORT: We describe a patient with Sjögren's syndrome who exhibited rapidly progressive cerebellar ataxia, nystagmus, cognitive decline, and psychiatric problems. Brain magnetic resonance imaging revealed marked atrophy of the cerebellum, and (18)F-fluorodeoxyglucose positron-emission tomography demonstrated glucose hypometabolism of the cerebellum. CONCLUSIONS: Our PSS patient exhibited a progressive course of cerebellar syndrome, as evidenced by cerebellar atrophy on serial brain images. Korean Neurological Association 2012-06 2012-06-29 /pmc/articles/PMC3391622/ /pubmed/22787501 http://dx.doi.org/10.3988/jcn.2012.8.2.155 Text en Copyright © 2012 Korean Neurological Association http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kim, Mi Jung Lee, Myoung Chong Lee, Jae-Hong Chung, Sun Ju Cerebellar Degeneration Associated with Sjögren's Syndrome |
title | Cerebellar Degeneration Associated with Sjögren's Syndrome |
title_full | Cerebellar Degeneration Associated with Sjögren's Syndrome |
title_fullStr | Cerebellar Degeneration Associated with Sjögren's Syndrome |
title_full_unstemmed | Cerebellar Degeneration Associated with Sjögren's Syndrome |
title_short | Cerebellar Degeneration Associated with Sjögren's Syndrome |
title_sort | cerebellar degeneration associated with sjögren's syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391622/ https://www.ncbi.nlm.nih.gov/pubmed/22787501 http://dx.doi.org/10.3988/jcn.2012.8.2.155 |
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