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首页> 外文期刊>British Journal of Haematology >Transplant-associated thrombotic microangiopathy and immune haematological complications following intestine-containing organ transplantation: experience from over 100 consecutive cases
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Transplant-associated thrombotic microangiopathy and immune haematological complications following intestine-containing organ transplantation: experience from over 100 consecutive cases

机译:含肠道器官移植后的移植相关的血栓形成微血管病和免疫血液学并发症:来自连续100个案例的经验

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Descriptions of passenger lymphocyte syndrome (PLS), immune cytopenias and transplant-associated thrombotic microangiopathy (TA-TMA) after intestine-containing transplants remain scarce. We describe our centre's experience of these complications from 2007 to 2019. Ninety-six patients received 103 transplants. PLS occurred in 9 (9%) patients (median 12 days post-transplant); all due to ABO antibodies. There were 31 minor ABO mismatch transplants. No patient required change in immunosuppression. Immune cytopenias (excluding PLS) occurred in six patients at an incidence of 1 center dot 7/100 patient years; three immune haemolysis, one immune thrombocytopenia, one acquired Glanzmann's and one immune neutropenia; 50% occurred with other cytopenias. All cases eventually responded to treatment, with a median of four treatments (range 1-8) and 5/6 were treated with rituximab. One patient with immune haemolysis required bortezomib. Complications were common in patients with immune cytopenias; 4/6 with infection needing intravenous antibiotics and 3/6 with venous thromboembolism. In 3/6 cases, a secondary cause for the immune cytopenia was evident. Switching from tacrolimus to ciclosporin was not necessary. There were five cases of transplant-associated thrombotic microangiopathy (TA-TMA; 1 center dot 5/100 patient years) requiring calcineurin inhibitor withdrawal; two cases associated with acute rejection. Two cases were managed with plasma exchange, one with plasma infusions and one with eculizumab. Further research in this patient group is required.
机译:在含肠道移植后的乘客淋巴细胞综合征(PLS),免疫细胞瘤和移植相关血栓性微盲(TA-TMA)的描述仍然稀缺。我们根据2007年至2019年描述了我们的中心对这些并发症的经验。九十六名患者接受了103名移植手术。 PLS发生在9名(9%)患者(移植后12天中位);所有因ABO抗体。有31个小abo错配移植。没有患者需要改变免疫抑制。免疫细胞缺乏症(不包括PLS)发生在六名患者中,其发病率为1中心DOT 7/100患者岁月;三种免疫溶血,一个免疫血小板减少症,一个收购格兰兹曼和一个免疫中性蛋白; 50%发生其他细胞缺陷。所有病例最终响应治疗,中间有四种治疗(范围1-8)和5/6均用Rituximab处理。一个免疫溶解的患者需要Bortezomib。在免疫细胞缺乏症患者中,并发症是常见的; 4/6具有需要静脉抗生素和3/6具有静脉血栓栓塞的感染。在3/6例中,显着的免疫细胞缺乏的二次生原因很明显。没有必要从地克莫司切换到西霉菌。预科相关血栓微扰动(TA-TMA; 1中心点5/100患者患者患者需要钙素抑制剂抑制剂的五种情况;与急性排斥有关的两种病例。用血浆交换管理两种病例,一个血浆输注,一个含有生态蛋白酶。需要进一步研究该患者组。

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