Glanzmann’s Thrombasthenia in the Parturient Undergoing Cesarean Delivery- A Case Report and Discussion of Clinical Consideration

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Abstract

Glanzmann thrombasthenia (GT) is a rare hemorrhagic disorder characterized by the absence of IIb-IIIa platelet glycoprotein (GPIIbIIIa) on the platelet surface. Many GT patients experience recurrent bleeding and require frequent platelet transfusion. Therefore, they are at risk for alloimmunization against platelet glycoprotein or Human leucocyte antigen (HLA) epitopes resulting in platelet refractoriness and therapeutic failure. We report a unique case of GT in pregnancy at risk for severe postpartum hemorrhage due to anti-GP IIb/IIIa and anti-HLA antibodies and the use of pro-hemostatic agents to optimize outcomes. A multidisciplinary approach is essential to achieving the best possible outcomes for these patients.
剖宫产产妇Glanzmann血栓减少1例报告及临床探讨
Glanzmann血栓减少症(GT)是一种罕见的出血性疾病,其特征是血小板表面缺乏IIb-IIIa血小板糖蛋白(GPIIbIIIa)。许多GT患者反复出血,需要频繁输血小板。因此,他们有针对血小板糖蛋白或人类白细胞抗原(HLA)表位的同种异体免疫导致血小板难治性和治疗失败的风险。我们报告了一例独特的妊娠GT,由于抗gp IIb/IIIa和抗hla抗体而有严重产后出血的风险,并使用促止血药物来优化结果。多学科方法对于这些患者获得最佳可能结果至关重要。
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