Ballas S K, Caro J F, Miguel O
Transfusion. 1978 Mar-Apr;18(2):215-9. doi: 10.1046/j.1537-2995.1978.18278160587.x.
A 40-year-old white male with quinidine induced hemolytic anemia but no thrombocytopenia is described. Hemolysis was extravascular in nature and via the immune-complex mechanism. The quinidine antibody was an IgG immunoglobulin that did not activate complement.
本文描述了一名40岁的白人男性,患有奎尼丁诱发的溶血性贫血,但无血小板减少症。溶血本质上是血管外溶血,通过免疫复合物机制发生。奎尼丁抗体是一种IgG免疫球蛋白,不激活补体。