Bercovitz R S, Macy M, Ambruso D R
Bonfils Blood Center, Denver, CO, USA.
Immunohematology. 2013;29(1):15-8.
Although antibodies to antigens in the Rh blood group system are common causes of warm autoimmune hemolytic anemia, specificity for only the D antigen is rare in autoimmune hemolysis in pediatric patients. This case reports an anti-D associated with severe hemolytic anemia (Hb = 2.1 g/dL) in a previously healthy 14-month-old child who presented with a 3-day history of low-grade fevers and vomiting. Because of his severe anemia, on admission to the hospital he was found to have altered mental status, metabolic acidosis, abnormal liver function tests, and a severe coagulopathy. He was successfully resuscitated with uncrossmatched units of group O, D- blood, and after corticosteroid therapy he had complete resolution of his anti-D-mediated hemolysis.
尽管针对Rh血型系统中抗原的抗体是温抗体型自身免疫性溶血性贫血的常见病因,但在儿科患者的自身免疫性溶血中,仅对D抗原具有特异性的情况较为罕见。本病例报告了一名14个月大的既往健康儿童,其患有与严重溶血性贫血(血红蛋白=2.1 g/dL)相关的抗-D,该患儿有3天低热和呕吐病史。由于其严重贫血,入院时发现他存在精神状态改变、代谢性酸中毒、肝功能检查异常以及严重的凝血病。通过输注未交叉配型的O型、D阴性血成功对其进行了复苏,并且在接受皮质类固醇治疗后,他的抗-D介导的溶血完全消退。