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获得性再生障碍性贫血的发病机制及治疗 被引量:3

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摘要 近十年来,关于获得性再生障碍性贫血(AA)发病机制及治疗的研究有了很大进展,普遍公认的治疗方法有.免疫抑制剂联合治疗(IST)和同种异基因造血干细胞移植(Allo-SCT),使本病的预后有了明显的改善。儿童极严重再障的5年生存率已从20世纪80年代的37%上升到90年代的83%,年龄%20岁重型再障患者10年生存率达73%,21~30岁者达75%,31~40岁者达66%,〉40岁者达47%。以下将分述近年来在这方面的进展及临床应用。
作者 王耀平
出处 《国际输血及血液学杂志》 CAS 2009年第1期15-18,共4页 International Journal of Blood Transfusion and Hematology
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参考文献12

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同被引文献15

  • 1杨朴.环孢霉素A 康力龙治疗慢性再生障碍性贫血[J].医药论坛杂志,2004,25(16):15-16. 被引量:3
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  • 3Bing H,Siyi Y,Wei Z,et al.The use of anti-human T lymphocyte porcine immunoglobulin and cyclosporine a to treat patients with acquired severe aplastic anemia[J].Acta Haematol,2010,124(4):245-250.
  • 4Jiang S,Wang Y,Shi W,et al.The benefit of ATG in immunosuppressive therapy of children with moderate aplastic anemia[J].Pediatr Hematol Oncol,2009,26(5):313-320.
  • 5Chang MH,Kim KH,Kim HS,et al.Predictors of response to immunosuppressive therapy with antithymocyte globulin and cyclosporine and prognostic factors for survival in patients with severe aplastic anemia[J].Eur J Haematol,2010,84(2):154-159.
  • 6Kamio T,Ito E,Ohara A,et al.Relapse of aplastic anemia in children after immunosuppressive therapy:a report from the Japan Childhood Aplastic Anemia Study Group[J].Haematologica,2011,96(6):814-819.
  • 7Tichelli A,Schrezenmeier H,Socié G,et al.A randomized controlled study in patients with newly diagnosed severe aplastic anemia receiving antithymocyte globulin (ATG),cyclosporine,with or without G-CSF:a study of the SAA Working Party of the European Group for Blood and Marrow Transplantation[J].Blood,2011,117(17):4434-41.
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  • 9桑玉旗.环孢素A治疗再生障碍性贫血的疗效因素分析[J].临床血液学杂志,2008,21(3):268-269. 被引量:2
  • 10张乃红.环孢霉素A治疗再生障碍性贫血的疗效和机制[J].中华血液学杂志,1998,19(4):218-220. 被引量:79

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