Document Detail


Self-remitting and reversible parkinsonism associated with neuro-sweet disease.
MedLine Citation:
PMID:  20558943     Owner:  NLM     Status:  In-Process    
Abstract/OtherAbstract:
We describe a 72-year-old man who developed subacute onset parkinsonism caused by neuro-Sweet disease (NSD). Magnetic resonance imaging of this patient's brain suggested inflammation of the bilateral basal ganglia and amygdalae. Clinical symptoms and MRI findings gradually improved without medication. However, his parkinsonism recurred one month after discharge from the hospital, at which time he was treated with corticosteroids, resulting in improvement again. His clinical course and human leukocyte antigen typing suggested that he was suffering from NSD. This case is the first report of NSD presenting with self-remitting and reversible parkinsonism.
Authors:
Fumitoshi Niwa; Takahiko Tokuda; Masashi Kimura; Yumiko Azuma; Toshiki Mizuno; Masanori Nakagawa
Related Documents :
7383343 - Calcification of the basal ganglia following carbon monoxide poisoning.
19876633 - Germinoma in the basal ganglia with an abnormal karyotype: case report and review of th...
12678173 - Utility of an informational intranet in a radiology department.
Publication Detail:
Type:  Case Reports; Journal Article     Date:  2010-06-15
Journal Detail:
Title:  Internal medicine (Tokyo, Japan)     Volume:  49     ISSN:  1349-7235     ISO Abbreviation:  Intern. Med.     Publication Date:  2010  
Date Detail:
Created Date:  2010-06-18     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9204241     Medline TA:  Intern Med     Country:  Japan    
Other Details:
Languages:  eng     Pagination:  1201-4     Citation Subset:  IM    
Affiliation:
Department of Neurology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Pure red cell aplasia associated with imatinib-treated FIP1L1-PDGFRA positive chronic eosinophilic l...
Next Document:  A Japanese case of Fragile-X-associated tremor/ataxia syndrome (FXTAS).