Martin Burks, Christina S Warren, Thomas Lightfoot, Emmanuel A Fadeyi
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引用次数: 0
摘要
有文献记载,输注血小板会导致 RhD 同种免疫。然而,非 RhD 血小板同种异体免疫的发生率要低得多,而且血小板引起非 RhD 血小板同种异体免疫的风险也被认为极低,并且与水性浓缩血小板的关系最为密切。一名患有急性髓性白血病的 22 个月大的男性患者因血小板减少症接受了 99 毫升的血小板分离治疗。三个月后,他接受了抗体筛查、直接抗球蛋白试验(DAT)和红细胞基因型的实验室评估。抗体筛查结果呈阳性,确定为抗 E。直接抗球蛋白试验(DAT)为阴性,患者的红细胞基因型预测为 E 抗原阴性,而血小板供体预测为 E 抗原阳性。即使是 2 岁以下的患者,也有可能因血小板穿刺输血而产生非 RhD 抗原的同种免疫。
Anti-E alloimmunization from a platelet apheresis transfusion in a 22-month-old male with acute myeloid leukemia.
RhD alloimmunization from platelet transfusions have been documented in the literature. However, non-RhD platelet alloimmunization is much less frequent and the risk for non-RhD alloimmunization from platelets is thought to be extremely low and most associated with buffy coat pooled platelets. A 22-month-old male with acute myeloid leukemia received 99 mL apheresis platelets for thrombocytopenia. Three months later, an antibody screen, the direct antiglobulin test (DAT), and red blood cell (RBC) genotype were sent for laboratory evaluation. The antibody screen was positive, with anti-E identified. The DAT was negative and the RBC genotype of the patient was predicted to be negative for the E antigen whereas the platelet donor was predicted to be positive for E antigen. There is a risk of alloimmunization of non-RhD antigen from platelet pheresis transfusion even in a patient less than 2 years old.