Gerstner J B, Smith M J, Davis K D, Cimo P L, Aster R H
Am J Hematol. 1979;6(1):71-5. doi: 10.1002/ajh.2830060110.
The effect of platelet type-specific transfusion in posttranfusion purpura is reported. Seven days after receiving 4 units of whole blood during total hip replacement a 69-year-old woman developed fulminant thrombocytopenic purpura. Her undiluted serum inhibited the clot retraction of PlAl-positive but not PlAl-negative blood. Anti-PlAl titer of her serum, determined by 51Cr platelet lysis technique, was 1:64. The serum had no lytic activity against platelet-rich plasma from two PlAl-negative donors. No anti-HLA antibody was detectable in the serum by lymphocytotoxicity technique, and serum obtained prior to transfusions had no platelet lytic activity. Four units of PlAl-negative platelet concentrate were administered, the first instance in which this treatment has been used. No rise in platelet count ensued, and the patient succumbed to purpura. Exchange transfusion or plasmapheresis remain the treatments of choice.
本文报道了血小板特异性输血在输血后紫癜中的作用。一名69岁女性在全髋关节置换术中接受4单位全血输注7天后,出现暴发性血小板减少性紫癜。其未稀释血清抑制PlAl阳性血的血块回缩,但不抑制PlAl阴性血的血块回缩。采用51Cr血小板溶解技术测定,其血清抗PlAl滴度为1:64。该血清对两名PlAl阴性供者的富含血小板血浆无溶解活性。采用淋巴细胞毒性技术在血清中未检测到抗HLA抗体,输血前获得的血清无血小板溶解活性。输注了4单位PlAl阴性血小板浓缩液,这是首次使用这种治疗方法。血小板计数未升高,患者死于紫癜。换血疗法或血浆置换术仍是首选治疗方法。