Kretschmer V, Mueller-Eckhardt C, Pralle H, Mueller-Eckhardt G, Grosse-Wilde H
Vox Sang. 1979;37(3):166-9. doi: 10.1111/j.1423-0410.1979.tb02286.x.
The case of an 18-year-old male patient with aplastic anemia is reported who was successfully treated by platelets from his father, mother and uncle over a period 8 months because of the very rare constellation of HLA-A,B identity in the family. The patient deceased from uncontrollable septicemia.
报告了一例18岁再生障碍性贫血男性患者的病例,由于其家族中极为罕见的HLA - A、B型相同情况,在8个月的时间里接受了来自其父亲、母亲和叔叔的血小板治疗,最终该患者死于无法控制的败血症。