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小儿特发性血小板减少性紫癜(ITP)通常起病急且持续数月,其中10～20％经类固醇、免疫抑制剂和静注免疫球蛋白等治疗无效,而转为长期慢性患者。几家医学中心曾报道ITP在确诊多年甚至20年后可慢慢缓解。目前尚无文献对这些后期自愈者提供早期的和准确的确诊方法。皇家曼彻斯特等两所儿童医院报道了5例ITP患儿,均为女孩发病年
Children with idiopathic thrombocytopenic purpura (ITP) usually acute onset and lasted for several months, of which 10 to 20% steroids, immunosuppressive agents and intravenous immunoglobulin and other treatment ineffective, and into long-term chronic patients. Several medical centers have reported that ITP can be slowly relieved after many years or even 20 years of diagnosis. There is no literature to provide these early self-healing early and accurate diagnosis method. Five children with ITP were reported in two children’s hospitals, including Royal Manchester, which were all year-old girls