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免疫性血小板减少性紫癜(Immune Thrombocytopenic Purpura,ITP)是一种自体免疫性疾病,以持续性血小板减少(plt<100×109/L)及皮肤黏膜出血为特征。其发病机理一般认为是自身抗体导致血小板破坏增多和巨核细胞成熟障碍。现将近几年本病的治疗进展综述如下。
Immune Thrombocytopenic Purpura (Immune Thrombocytopenic Purpura, ITP) is an autoimmune disease characterized by persistent thrombocytopenia (plt <100 × 109 / L) and mucocutaneous bleeding. The pathogenesis is generally believed that autoantibodies lead to increased platelet destruction and megakaryocyte maturation disorders. In recent years, the progress of treatment of the disease are summarized below.