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首页> 外文期刊>Canadian journal of gastroenterology >Graft-versus-host disease after liver transplantation complicated by systemic aspergillosis with pancarditis.
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Graft-versus-host disease after liver transplantation complicated by systemic aspergillosis with pancarditis.

机译:肝移植术后并发全身性曲霉病伴全心炎的移植物抗宿主病。

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Graft-versus-host disease after liver transplantation complicated by systemic aspergillosis with pancarditis. Can J Gastroenterol 2000;14(7):637-640. Acute graft-versus-host disease (GVHD) is a common complication after bone marrow transplantation, with characteristic rash and diarrhea being the most common features. After liver transplantation, however, this phenomenon is very rare. Most transplant patients are on a variety of medications, including immunosuppressants; therefore, the differential diagnosis of skin rash or diarrhea is broad. A 37-year-old man who underwent liver transplantation for primary biliary cirrhosis, and developed a rash and watery diarrhea, is presented. Skin and colonic biopsies confirmed acute GVHD. A pulse of intravenous steroids was given. The skin rash improved, but he developed pancytopenia. His course was complicated by central line infection, jugular and subclavian vein thrombosis, pseudomembranous colitis, recurrent bacteremia, cholestasis on total parenteral nutrition and cytomegalovirus infection. After the onset of pleuritic chest pain and clinical sepsis, spiral computed tomography scan of his chest and abdomen revealed septic infarcts in multiple organs. Despite empirical treatment with amphotericin B, he died of multiorgan dysfunction syndrome within 72 h. Autopsy revealed systemic aspergillosis with pancarditis, endocardial vegetations, and septic pulmonary, splenic, hepatic and renal infarcts. The pathogenesis and experience with this rare, but often fatal, complication of liver transplantation are reviewed. In contrast to GVHD after bone marrow transplantation, pancytopenia is common and liver dysfunction is rare. One should have a high level of suspicion in the liver transplant recipient presenting with rash and/or diarrhea.
机译:肝移植术后并发全身性曲霉病伴全心炎的移植物抗宿主病。 Can J胃肠2000; 14(7):637-640。急性移植物抗宿主病(GVHD)是骨髓移植后的常见并发症,最典型的特征是皮疹和腹泻。但是,在肝移植后,这种现象非常罕见。大多数移植患者正在使用多种药物,包括免疫抑制剂。因此,皮疹或腹泻的鉴别诊断范围很广。介绍了一个因原发性胆汁性肝硬化而接受肝移植,出现皮疹和水样腹泻的37岁男子。皮肤和结肠活检证实为急性GVHD。给予了静脉内的类固醇脉冲。皮疹有所改善,但他出现了全血细胞减少症。他的病程并发,包括中线感染,颈和锁骨下静脉血栓形成,假膜性结肠炎,复发性菌血症,总肠外营养胆汁淤积和巨细胞病毒感染。胸膜炎胸痛和临床败血症发作后,他的胸部和腹部的螺旋计算机断层扫描扫描显示了多个器官中的败血症性梗塞。尽管使用两性霉素B进行了经验性治疗,但他仍在72小时内死于多器官功能障碍综合症。尸检显示全身性曲霉病,并伴有心包炎,心内膜植被和败血性肺,脾,肝和肾梗塞。本文回顾了这种罕见但通常致命的肝移植并发症的发病机理和经验。与骨髓移植后的GVHD相比,全血细胞减少症很常见,肝功能障碍很少见。在肝移植受者中出现皮疹和/或腹泻应高度怀疑。

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