Marzusch K, Fischer J, Dietl J, Wiest E, Völklein K, Schnaidt M
Department of Obstetrics and Gynecology, University of Tübingen, Germany.
Acta Obstet Gynecol Scand. 1993 Oct;72(7):583-5. doi: 10.3109/00016349309058169.
In this paper we present a patient with an initially questionable history of neonatal alloimmune thrombocytopenia (NAT) due to materno-fetal HPA-1a (PLA1) incompatibility. No circulating antibodies were detectable in untreated maternal serum, but an adsorption/elution technique enabled the demonstration of the platelet-specific anti-HPA-1a (anti-PLA1) in maternal serum. Cordocentesis at 35 weeks of gestation revealed a fetal platelet count of 18 x 10(9)/l. Intrauterine platelet transfusion with HPA-1a (PLA1)-negative donor platelets was performed prior to cesarean section.
在本文中,我们报告了一名患者,其最初因母胎HPA-1a(PLA1)不相容而有新生儿同种免疫性血小板减少症(NAT)的可疑病史。未经治疗的母体血清中未检测到循环抗体,但吸附/洗脱技术证实母体血清中存在血小板特异性抗HPA-1a(抗PLA1)。妊娠35周时进行脐血穿刺,显示胎儿血小板计数为18×10⁹/L。剖宫产术前进行了HPA-1a(PLA1)阴性供体血小板的宫内血小板输注。