Catastrophic Antiphospholipid Syndrome after Orthotopic Liver Transplant

R. Okeke, J. Lok, R. Wells, M. Wycoff, A. Engelhardt, J. Bettag, C. O'Leary, T. Hallcox, M. Nazzal
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Abstract

Background Catastrophic antiphospholipid syndrome (CAPS) is an autoimmune thrombogenic disorder of small and large vessels caused by autoantibodies against phospholipids and phospholipid-binding proteins. This severe form of antiphospholipid syndrome (APS) presents clinically with simultaneous life-threatening multiorgan thrombosis and the presence of two or more persistent antiphospholipid antibodies (APL) confirmed on testing 12 weeks apart. Case Presentation. We describe a case report of a 66-year-old woman with detected antinuclear antibodies (ANA) pretransplant diagnosed with CAPS following orthotopic liver transplant. The patient had acute respiratory failure; Doppler ultrasound and CT angiogram confirmed thrombosis in the hepatic artery, subsequent occlusion of the jump graft, and a splenic infarct. Hypercoagulability workup showed elevated levels of anticardiolipin IgG and beta-2-glycoprotein IgG/IgM and positive lupus anticoagulant, treated with steroids and anticoagulation. The patient was discharged after one month and was transitioned from heparin to life-long warfarin. Conclusion Our patient provided a standard presentation of CAPS with abnormal pretransplant levels of antinuclear antibodies (ANA). Although there have been studies investigating the relationship between anticardiolipin antibodies and lupus anticoagulants and APS, the relationship between pretransplant positive ANA or antimitochondrial antibodies (AMA) and CAPS has yet to be explored. Further studies will be needed to determine the significance of these antibodies. We recommend preoperative APL testing for patients with positive ANA and AMA at preliver transplant presentation.
原位肝移植后的灾难性抗磷脂综合征
灾难性抗磷脂综合征(CAPS)是由针对磷脂和磷脂结合蛋白的自身抗体引起的小血管和大血管自身免疫性血栓性疾病。这种严重形式的抗磷脂综合征(APS)在临床上表现为同时危及生命的多器官血栓形成,并且存在两种或两种以上的持续抗磷脂抗体(APL),间隔12周检测证实。案例演示。我们报告了一例66岁的女性,在移植前检测到抗核抗体(ANA),诊断为原位肝移植后的CAPS。患者出现急性呼吸衰竭;多普勒超声和CT血管造影证实肝动脉血栓形成,随后跳跃移植物闭塞,脾梗死。高凝检查显示抗心磷脂IgG和β -2糖蛋白IgG/IgM水平升高,狼疮抗凝剂阳性,类固醇和抗凝治疗。患者一个月后出院,由肝素转为终身华法林。结论本例患者具有标准的移植前抗核抗体(ANA)水平异常的CAPS。虽然已有研究探讨了抗心磷脂抗体与狼疮抗凝剂和APS之间的关系,但移植前ANA或抗线粒体抗体(AMA)阳性与CAPS之间的关系尚待探讨。需要进一步的研究来确定这些抗体的意义。我们建议在肝移植前对ANA和AMA阳性患者进行术前APL检测。
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