[Neonatal alloimmune thrombocytopenia due to a rare anti-HPA-1b antibody].

P Moosmann, J C Fauchère, J Halter, D Binder, U Schanz
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Abstract

Foetal and neonatal alloimmune thrombocytopenia is caused by transplacental transfer of antibodies directed against platelet antigens and affects approximately 1 in 1000-2500 neonates. Clinically relevant complications are the intracranial haemorrhages that occur in 10-20% of cases. 20 platelet antigen systems are currently known. However, immunisation is most frequently seen against two of these (HPA-1a and HPA-5b). Treatment options include transfusion of compatible or, if these are not available while urgently needed, random donor platelets, intravenous immunoglobulin, and steroids. We report on a case of neonatal alloimmune thrombocytopenia due to an anti-HPA-1b antibody in the third pregnancy of a 31-year-old Caucasoid woman. The infant was treated with repeated maternal and random donor platelet transfusions and with a single dose of intravenous immunoglobulin.

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[罕见的抗hpa -1b抗体引起的新生儿同种免疫性血小板减少症]。
胎儿和新生儿同种免疫性血小板减少症是由针对血小板抗原的抗体经胎盘转移引起的,大约1000-2500名新生儿中有1人受其影响。临床相关并发症为颅内出血,发生率为10-20%。目前已知的血小板抗原系统有20种。然而,最常见的免疫是针对其中两种(HPA-1a和HPA-5b)。治疗方案包括输注相容的血小板,或在急需时无法获得的随机供体血小板,静脉注射免疫球蛋白和类固醇。我们报告一例新生儿同种免疫性血小板减少症由于抗hpa -1b抗体在第三次怀孕的31岁高加索妇女。该婴儿接受了反复的母体和随机供体血小板输注以及单剂量静脉注射免疫球蛋白的治疗。
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