MTHFR缺乏和肝素诱发的血小板减少症患者活体肾移植成功一例报告

Dong Kang, Hanbi Lee, B. Chung, B. Choi, Chul-woo Yang, E. Ko
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引用次数: 0

摘要

肝素诱导的血小板减少肾移植受者的围手术期抗凝是具有挑战性的,因为矛盾的高凝性。患者49岁,终末期肾病,既往有中风史,接受活体肾移植。第5次透析后,血小板计数降至10000 /μL,立即停用肝素。5天后确诊为肺血栓栓塞伴深静脉血栓形成。发现抗肝素PF4抗体,血清同型半胱氨酸升高,亚甲基四氢叶酸还原酶基因突变。随后的冠状动脉造影显示三支血管病变。给予阿哌沙班、叶酸、阿司匹林和氯吡格雷,并植入下腔静脉过滤器。此后,冠状动脉搭桥手术使用阿加曲班桥无并发症。3个月后采用阿加曲班方案进行肾移植。移植肾功能良好,无并发症。总之,我们通过建立个体化围手术期抗凝治疗方案,成功地对一名患有亚甲基四氢叶酸还原酶缺乏和肝素诱导的血小板减少症的嗜血栓患者进行了肾移植。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful Living Donor Kidney Transplantation in a Patient with MTHFR Deficiency and Heparin-Induced Thrombocytopenia: A Case Report
Perioperative anticoagulation in a kidney transplant recipient with heparin-induced thrombocytopenia is challenging due to paradoxical hypercoagulability. A 49-year-old man with end-stage kidney disease and a previous stroke history was referred for living donor kidney transplantation. After the fifth dialysis session, the platelet count decreased to 10,000/μL, and heparin was immediately discontinued. Five days later, pulmonary thromboembolism with deep vein thrombosis was identified. Anti-heparin PF4 antibody, elevated serum homocysteine, and methylenetetrahydrofolate reductase gene mutations were discovered. Subsequent coronary angiography revealed three-vessel disease. Apixaban, folate, aspirin, and clopidogrel were administered and an inferior vena cava filter was implanted. Thereafter, coronary artery bypass graft surgery was performed using argatroban-bridging without complications. Kidney transplantation was performed 3 months later using the argatroban protocol. The graft kidney functioned well without any complications. In conclusion, we successfully conducted kidney transplantation in a thrombophilic patient with a methylenetetrahydrofolate reductase deficiency and heparin-induced thrombocytopenia by establishing an individualized perioperative anticoagulation protocol.
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