产后获得性血友病(PAH) -一种罕见的疾病

S. Khan, Saima Siddiqui, Q. Abedin
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摘要

目的:获得性血友病A (AHA)是一种罕见的自身免疫性疾病,可导致危及生命的出血。凝血因子VIII自身抗体(抑制剂)的形成导致出血性综合征,可能出现在任何年龄;然而,AHA的患病率主要见于产后和老年人。特发性获得性血友病是最常见的获得性血友病类型,但它也与自身免疫性疾病、恶性肿瘤、药物和疫苗接种有关。产后获得性血友病(PAH)可能由于胎儿FVIII抗体的发展而发展。在这个病例报告中,36岁的亚洲女性主诉2个月的瘀伤。四个月前有剖宫产史。家族史、既往病史和用药史无显著性差异。由于没有活动性出血,患者开始口服强的松龙和硫唑嘌呤,并被告知有关疾病和预防措施。患者于2周后出现严重静脉出血,自行药物流产后继发贫血。为此,她接受细胞群和低温沉淀。继续使用类固醇和硫唑嘌呤治疗,出院时病情稳定。她的超声骨盆显示小肌瘤。病人回到她的村庄,在那里她再次出现严重的PV出血,为此她接受了子宫切除术。患者在我院就诊时伴有严重的手术部位出血、疼痛和贫血。患者接受包装红细胞(prbc)、新鲜冷冻血浆(FFP)、重组活化凝血因子VII (rFVIIa)、强的松龙IV和硫唑嘌呤PO治疗。持续监测部分凝血活蛋白、血红蛋白活性。一周后出血停止,但活化部分凝血活素时间(APTT)仍延长,因此我们逐渐减少rfvia剂量并建议进行两次血浆置换。APTT、血红蛋白水平、抑制剂滴度、高敏C反应蛋白(hs-CRP)水平均有改善。患者出院时病情稳定,并被建议在支持护理和伤口包扎的情况下继续在家用药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Postpartum Acquired Hemophilia (PAH) – A Rare Entity
Objective: Acquired Hemophilia A (AHA) is a rare autoimmune disease that can result in life threatening bleeding. Formation of auto-antibodies (inhibitors) against coagulation factor VIII develops the hemorrhagic syndrome that may appear at any age; however, prevalence of AHA is chiefly observed in post-partum and elderly persons. Idiopathic acquired hemophilia is commonest type of acquired hemophilia whereas it is also associated with autoimmune disease, malignant neoplasm, medication and vaccinations. Post-partum acquired hemophilia (PAH) may develop due to development of antibodies against fetal FVIII. In this case report, 36-year-old Asian woman presented with complain of bruises from 2 months. There was history of cesarean section four months ago. Family history, past medical and drug history were not significant. As there was no active bleeding, patient was started an oral prednisolone along with azathioprine and was counseled regarding disease and precautions. Patient presented after 2 weeks with severe PV bleed, anemia secondary to self-induced medicine abortion. For this she receives pack cells and cryoprecipitate. Steroids and azathioprine were continued and patient was discharged in stable condition. Her ultrasound pelvis however showed small fibroids. Patient went back to her village where she again develops severe PV bleed and for that she underwent hysterectomy. Patient presented in our hospital with severe operative site bleeding, pain and anemia. She was managed with Packed Red Blood (PRBCs), Fresh Frozen Plasma (FFP), Recombinant Activated Clotting Factor VII (rFVIIa), prednisolone IV and azathioprine PO. Her Activated Partial Thromboplastin, Hemoglobin were continuously monitored. After a week bleeding was stopped but Activated Partial Thromboplastin Time (APTT) was still prolonged so we tapered rFVIIa dose and advice two sessions of plasmapheresis. APTT, hemoglobin levels, inhibitor titer, High-Sensitivity C – reactive protein (hs-CRP) levels were improved. Patient was discharged in a stable condition and was advised to continue medication at home with supportive care and wound dressing.
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