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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...

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Detalles Bibliográficos
Autores principales: Kim, Mi Jung, Lee, Myoung Chong, Lee, Jae-Hong, Chung, Sun Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2012
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.
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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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