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Anti-MDA5 Antibody-positive Dermatomyositis Complicated by Autoimmune-associated Hemophagocytic Syndrome That Was Successfully Treated with Immunosuppressive Therapy and Plasmapheresis
http://hdl.handle.net/10069/38763
http://hdl.handle.net/10069/387631337e02b-9123-458b-b2a2-d9a614db8a1f
名前 / ファイル | ライセンス | アクション |
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IntMed57_3473.pdf (1.8 MB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2019-01-09 | |||||
タイトル | ||||||
タイトル | Anti-MDA5 Antibody-positive Dermatomyositis Complicated by Autoimmune-associated Hemophagocytic Syndrome That Was Successfully Treated with Immunosuppressive Therapy and Plasmapheresis | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Anti-MDA5 antibody-positive dermatomyositis | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Autoimmune disease | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Corticosteroid therapy | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Cyclophosphamide | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Hemophagocytic syndrome | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Plasmapheresis | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
著者 |
Fujita, Yuya
× Fujita, Yuya× Fukui, Shoichi× Suzuki, Takahisa× Ishida, Midori× Endo, Yushiro× Tsuji, Sousuke× Takatani, Ayuko× Igawa, Takashi× Shimizu, Toshimasa× Umeda, Masataka× Sumiyoshi, Remi× Nishino, Ayako× Koga, Tomohiro× Kawashiri, Shin-ya× Iwamoto, Naoki× Ichinose, Kunihiro× Tamai, Mami× Nakamura, Hideki× Origuchi, Tomoki× Abe, Kuniko× Kawakami, Atsushi |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | A 56-year-old Japanese woman with muscle weakness, increased creatine kinase and aldolase levels, and characteristic cutaneous lesions was diagnosed with anti-melanoma differentiation-associated gene 5 antibody (anti-MDA5 antibody)-positive dermatomyositis. She also had interstitial lung disease (ILD). After corticosteroid and tacrolimus combination therapy was started, bicytopenia and elevated serum ferritin and trans-aminase emerged. Because the bone marrow tissues were hypoplastic with hemophagocytes, she was diagnosed with concomitant autoimmune-associated hemophagocytic syndrome (HPS). Intravenous cyclophosphamide pulse therapy and plasmapheresis were performed. The laboratory findings indicated improved abnormalities, and the ILD did not progress. Anti-MDA5 antibody-positive dermatomyositis can be complicated by HPS. |
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書誌情報 |
Internal Medicine 巻 57, 号 23, p. 3473-3478, 発行日 2018-07-06 |
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出版者 | ||||||
出版者 | 日本内科学会 | |||||
出版者別言語 | ||||||
Japanese Society of Internal Medicine | ||||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 09182918 | |||||
EISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 13497235 | |||||
DOI | ||||||
関連タイプ | isIdenticalTo | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.2169/internalmedicine.1121-18 | |||||
権利 | ||||||
権利情報 | c2018 The Japanese Society of Internal Medicine. The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). | |||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | Internal Medicine, 57(23), pp.3473-3478; 2018 |