Early induction of plasma exchange and immunosuppression therapy was effective in a child with anti-muscle-specific kinase positive myasthenia gravis : a case report
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- Asai Hiroshi
- Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka
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- Ishii Masahiro
- Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka
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- Shimono Masayuki
- Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka
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- Igarashi Ryota
- Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka
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- Matsuda Yumeko
- Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka
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- Fukuda Tomofumi
- Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka
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- Senju Ayako
- Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka
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- Takano Shiho
- Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka
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- Shiota Naoki
- UBE Industries, LTD. Department of Health Care & Support Center, Environment, Ube, Yamaguchi
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- Kusuhara Koichi
- Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka
Bibliographic Information
- Other Title
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- 早期の単純血漿交換療法と免疫抑制剤導入が有効であった抗筋特異的チロシンキナーゼ (MuSK) 抗体陽性重症筋無力症の1例
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Description
<p> We report the case of a 12 year-old girl with anti-muscle-specific kinase (MuSK) positive myasthenia gravis (MG). She exhibited ptosis, dysphagia, and facial muscle weakness and was tested positive for MuSK autoantibodies. She was initially treated with methylprednisolone pulse therapy ; however, her symptoms persisted. She then underwent five sessions of plasma exchange, which was very effective. Subsequently, she was prescribed oral tacrolimus and has maintained complete stable remission for 2 years. Aggressive treatments including the early induction of plasma exchange and immunosuppression therapy may be effective for childhood-onset anti-MuSK positive MG.</p>
Journal
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- NO TO HATTATSU
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NO TO HATTATSU 50 (4), 288-291, 2018
The Japanese Society of Child Neurology
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Details 詳細情報について
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- CRID
- 1390001288056987264
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- NII Article ID
- 130007435989
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- ISSN
- 18847668
- 00290831
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- Text Lang
- ja
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed