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关于获得性血友病A诊断与治疗国际建议的解读 被引量:2

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摘要 获得性血友病A(AHA)是一种少见病,发病率大约每年1.5/10万,以循环中出现抗FⅦ的自身抗体为特征,可导致无出血病史的患者发生自发性出血。约50%患者伴自身免疫性疾病、实体瘤、淋巴细胞增殖性疾病和妊娠等。由于该病出血症状具有异质性,临床表现从致命性外伤出血到轻微出血,甚至无出血倾向等。
作者 张磊 杨仁池
出处 《国际输血及血液学杂志》 CAS 2010年第2期172-175,共4页 International Journal of Blood Transfusion and Hematology
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  • 1周立红,刘泽霖.获得性血友病[J].血栓与止血学,2007,13(1):33-35. 被引量:4
  • 2勋1lshanskyLB,KippsSP.威廉姆斯血液病学[M].陈竺,陈赛娟,译.8版.北京:人民卫生出版社,2011:1941.1944.
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  • 6Toschi V, Baudo F. Diagnosis, laboratory aspects and management of acquired hemophilia A[J]. Intem Emerg Med, 2010, 5(4): 325-333.
  • 7Collins P, Baudo F, Knoebl P, et al. Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)[J]. Blood, 2012,120(1): 47-55.
  • 8Collins PW, Hirsch S, Baglin TP, et al. Acquired hemophilia A in the United Kingdom: a 2-year National surveillance study by the United Kingdom Haemophilia Centre Doctors' Organisation[J]. Blood, 2007,109(5): 1870-1877.
  • 9Franchini M, Targher G, Manzato F, et al. Acquired factor vm inhibitors in oncohematology: a systematic review[J]. Crit Rev Oncol Hematol, 2008, 66(3): 194-199.
  • 10Aouba A, Rey G, Pavillon G, et al. Deaths associated with acquired haemophilia in France from 2000 to 2009: multiple cause analysis for best care strategies[J]. Haemophilia, 2012, 18(3): 339-344.

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