- Author:
Mi Jung KIM
1
;
Myoung Chong LEE
;
Jae Hong LEE
;
Sun Ju CHUNG
Author Information
- Publication Type:Case Report
- Keywords: Sjogren's syndrome; cerebellar degeneration; ataxia; cognitive impairment
- MeSH: Ataxia; Atrophy; Brain; Cerebellar Ataxia; Cerebellar Diseases; Cerebellum; Glucose; Humans; Magnetic Resonance Imaging; Neurologic Manifestations; Polyneuropathies; Positron-Emission Tomography; Sjogren's Syndrome
- From:Journal of Clinical Neurology 2012;8(2):155-159
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND: Neurologic manifestations of primary Sjogren'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 Sjogren'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 18F-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.