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免疫性血小板减少症的免疫异常特征与治疗进展 被引量:4

Progress of the Immune Dysfunction and Treatment of Immune Thrombocytopenia
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摘要 免疫性血小板减少症(immune thrombocytopenia,ITP)是一种由体液免疫和细胞免疫异常导致血小板破坏增多、生成减少、临床上以皮肤黏膜出血为特征的血小板减少性疾病[1],成人发病率约为5~10/10万[2],儿童年发病率为1.9~6.4/10万[3].自身抗体介导的血小板破坏是ITP的发病基础.自身抗体使ITP患者的血小板仅存在数小时就会被迅速清除,远远短于正常人血小板寿命.
作者 闪丹 顾健
出处 《血栓与止血学》 2013年第6期283-287,共5页 Chinese Journal of Thrombosis and Hemostasis
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参考文献50

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二级参考文献8

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共引文献21

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