Fisher Syndrome Associated with Immune Thrombocytopenic Purpura
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概要
- 論文の詳細を見る
We describe a 51-year-old man with Fisher syndrome (FS) and immune thrombocytopenic purpura (ITP) that developed after upper respiratory infection (URI). Laboratory investigations demonstrated immunoglobulin (Ig) G class of anti-GQ1b autoantibody and reduced platelet count with platelet-associated IgG, which spontaneously improved in parallel with neurologic symptoms. Thus the possible association of ITP should be considered when encountering a patient with FS. This patient suggests that there may be a certain infectious agent causing URI, leading to the co-occurrence of FS and ITP.
著者
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Furukawa Yutaka
Department Of Biochemistry And Molecular Biology Saitama University
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Yamada Masahito
Department Of Neurology & Neurobiology Of Aging Kanazawa University Graduate School Of Medical S
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Iwasa Kazuo
Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Japan
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Furukawa Yutaka
Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Japan
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Ono Kenjiro
Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Japan
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