Ozsoylu S, Karabent A, Irken G, Tuncer M
Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Am J Hematol. 1991 Feb;36(2):82-5. doi: 10.1002/ajh.2830360203.
Antiplatelet antibodies were shown by the Handin and Stossel method in the sera of all 103 patients with acute idiopathic thrombocytopenic purpura (ITP) and in 100 cases following recovery from it. These antibodies were also shown in the sera of all 46 patients with chronic ITP and 32 cases after recovery. The decrease in level of antiplatelet antibodies was significant in all these children following recovery (P less than 0.001 for acute ITP, P less than 0.05 for chronic ITP). Antiplatelet antibodies could be determined in 67 acute and 21 chronic ITP cases in thrombocytopenic phase and following recovery, which showed very significant decreases in levels in each case in a later period. Antiplatelet antibody levels corresponding to the thrombocytopenic phase and recovery in acute and chronic ITP were significantly higher than normal and thrombocytopenic control values (P less than 0.001 for each).
采用汉丁和斯托塞尔方法在103例急性特发性血小板减少性紫癜(ITP)患者的血清中以及100例康复后的患者血清中均检测到抗血小板抗体。在46例慢性ITP患者的血清中以及32例康复后的患者血清中也检测到了这些抗体。所有这些患儿康复后抗血小板抗体水平均显著下降(急性ITP患者P<0.001,慢性ITP患者P<0.05)。在血小板减少期及康复后的67例急性ITP患者和21例慢性ITP患者中均可检测到抗血小板抗体,且后期各病例的抗体水平均显著下降。急性和慢性ITP患者血小板减少期及康复期的抗血小板抗体水平均显著高于正常对照值和血小板减少对照值(每组P<0.001)。