ID | 115679 |
タイトル別表記 | Clinical Guides for aHUS
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著者 |
Kato, Hideki
The University of Tokyo
Nangaku, Masaomi
The University of Tokyo
Hataya, Hiroshi
Tokyo Metropolitan Children’s Medical Center
Sawai, Toshihiro
Shiga University of Medical Science
Ashida, Akira
Osaka Medical College
Fujimaru, Rika
Osaka City General Hospital
Hidaka, Yoshihiko
Shinshu University
Kaname, Shinya
Kyorin University
Maruyama, Shoichi
Nagoya University
Yasuda, Takashi
Kichijoji Asahi Hospital
Yoshida, Yoko
The University of Tokyo
Ito, Shuichi
Yokohama City University
Hattori, Motoshi
Tokyo Women’s Medical University
Miyakawa, Yoshitaka
Saitama Medical University
Fujimura, Yoshihiro
Nara Medical University
Okada, Hirokazu
Saitama Medical University
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キーワード | alternative complement pathway
atypical hemolytic uremic syndrome
eculizumab
thrombotic microangiopathy
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資料タイプ |
学術雑誌論文
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抄録 | Atypical hemolytic uremic syndrome (aHUS) is a rare disease characterized by the triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. In 2013, we developed diagnostic criteria to enable early diagnosis and timely initiation of appropriate treatment for aHUS. Recent clinical and molecular findings have resulted in several proposed classifications and definitions of thrombotic microangiopathy and aHUS. Based on recent advances in this field and the emerging international consensus to exclude secondary TMAs from the definition of aHUS, we have redefined aHUS and proposed diagnostic algorithms, differential diagnosis, and therapeutic strategies for aHUS.
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掲載誌名 |
Pediatrics International
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ISSN | 1442200X
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出版者 | Japan Pediatric Society|Wiley
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巻 | 58
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号 | 7
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開始ページ | 549
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終了ページ | 555
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発行日 | 2016-07-26
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権利情報 | This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License(https://creativecommons.org/licenses/by-nc/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
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言語 |
eng
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著者版フラグ |
出版社版
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部局 |
医学系
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