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Rapid progression and brain atrophy in anti-AMPA receptor encephalitis
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Rapid progression and brain atrophy in anti-AMPA receptor encephalitis

Yi-Chia Wei, Chi-Hung Liu, Jainn-Jim Lin, Kun-Ju Lin, Ko-Lun Huang, Tsong-Hai Lee, Yeu-Jhy Chang, Tsung-I Peng, Kuang-Lin Lin, Ting-Yu Chang, …
Journal of Neuroimmunology, 卷.261(1-2), 頁碼.129-133
08/2013
PMID: 23796872

摘要

AMPA Anti-glutamate receptor Brain atrophy Encephalitis Eosinophilic meningoencephalitis Immunology and Allergy Immunology Neurology Neurology (clinical)
Anti-α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor encephalitis is an anti-neuronal surface antigen autoimmune encephalitis that is rarely reported. Our study evaluated the first known patient who developed anti-AMPA receptor encephalitis during pregnancy. Initial brain MRI revealed bilateral limbic encephalitis. However, rapid brain atrophy on MRI with extensive hypometabolism of cerebral cortices, caudate nuclei and brain stem hypoperfusion on 18 F-FDG PET developed when clinically progressed. IgG index of serial CSF studies reflected the clinical improvements after plasmapheresis and plasma exchange. The clinical spectrum of anti-AMPA receptor encephalitis may be expanded from limited limbic involvement to extended central nervous system. © 2013 Elsevier B.V.

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