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- Furukawa Yutaka
- Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Japan Department of Neurology, National Hospital Organization Iou National Hospital, Japan
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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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- Ono Kenjiro
- Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Japan
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- Yamada Masahito
- Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Japan
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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.<br>
収録刊行物
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- Internal Medicine
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Internal Medicine 50 (6), 631-633, 2011
一般社団法人 日本内科学会
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詳細情報 詳細情報について
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- CRID
- 1390001204871128960
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- NII論文ID
- 130000649898
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- ISSN
- 13497235
- 09182918
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- 本文言語コード
- en
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- データソース種別
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- JaLC
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- 抄録ライセンスフラグ
- 使用不可