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原位肝移植术后新发炎症性肠病5例。

Five cases of de novo inflammatory bowel disease after orthotopic liver transplantation.

作者信息

Wörns Marcus A, Lohse Ansgar W, Neurath Markus F, Croxford Andrew, Otto Gerd, Kreft Andreas, Galle Peter R, Kanzler Stephan

机构信息

First Department of Internal Medicine, Johannes Gutenberg-University Mainz, Germany.

出版信息

Am J Gastroenterol. 2006 Aug;101(8):1931-7. doi: 10.1111/j.1572-0241.2006.00624.x. Epub 2006 Jun 22.

Abstract

Immunosuppression is currently the treatment of choice for severe inflammatory bowel disease (IBD). Thus, it was anticipated that the course of preexisting IBD should improve after orthotopic liver transplantation (OLT). Despite sufficient allograft immunosuppressive therapy, however, exacerbation of IBD or the development of de novo IBD after OLT were described in some cases, primarily in patients transplanted for end-stage primary sclerosing cholangitis (PSC). In addition, the development of de novo IBD in patients undergoing OLT for indications other than PSC was described. Evaluating our collective of 314 liver transplanted patients we found five patients transplanted for various indications other than PSC (autoimmune hepatitis [AIH], acute-on-chronic hepatitis B, Wilson's disease, and cryptogenic cirrhosis) who developed de novo IBD after OLT despite sufficient immunosuppressive therapy with tacrolimus or cyclosporine. PSC was widely excluded in these patients by clinical and histological examinations and there was no sign of an enteric infection. It was remarkable that all patients were suspected to have an autoimmune background. Four of our patients were women and almost all patients showed histologically typical signs of an ulcerative colitis (UC). To prevent allograft rejection, three of five patients were treated with cyclosporine and the other two with tacrolimus. After diagnosis, treatment with aminosalicylates and corticosteroids led to complete clinical and histological remission. However, relapses occurred frequently after termination of specific therapy. In combination with previous reports, our cases indicate an immune dysregulation leading to the development of de novo IBD after OLT under immunosuppressive therapy. Reviewing the literature, it should be considered that apart from the autoimmune background, immunosuppressive therapy may itself play a major role in the development of de novo IBD. From the clinical point of view, it is of critical importance to detect this phenomenon, since diarrhea is an important cause of morbidity and mortality in transplanted patients and therapy for this disorder completely differs from the treatment for other causes of diarrhea. Aminosalicylates and courses of corticosteroids offer an effective treatment.

摘要

免疫抑制目前是重症炎症性肠病(IBD)的首选治疗方法。因此,预计原位肝移植(OLT)后,原有IBD的病程应有所改善。然而,尽管进行了充分的同种异体移植免疫抑制治疗,但在某些情况下,OLT后仍有IBD加重或新发IBD的情况出现,主要发生在因终末期原发性硬化性胆管炎(PSC)接受移植的患者中。此外,也有接受OLT的患者因PSC以外的其他适应症而新发IBD的报道。在评估我们收集的314例肝移植患者时,我们发现有5例因PSC以外的各种适应症(自身免疫性肝炎[AIH]、慢性乙型肝炎急性发作、威尔逊病和隐源性肝硬化)接受移植的患者,尽管使用他克莫司或环孢素进行了充分的免疫抑制治疗,但在OLT后仍新发了IBD。通过临床和组织学检查,这些患者被广泛排除患有PSC,且没有肠道感染的迹象。值得注意的是,所有患者都被怀疑有自身免疫背景。我们的患者中有4名女性,几乎所有患者在组织学上都表现出溃疡性结肠炎(UC)的典型症状。为防止同种异体移植排斥反应,5名患者中有3名接受了环孢素治疗,另外2名接受了他克莫司治疗。诊断后,使用氨基水杨酸酯类药物和皮质类固醇进行治疗,使临床和组织学完全缓解。然而,在特定治疗终止后,复发频繁出现。结合之前的报道,我们的病例表明免疫失调会导致在免疫抑制治疗下OLT后新发IBD。回顾文献,应考虑到除自身免疫背景外,免疫抑制治疗本身可能在新发IBD的发生中起主要作用。从临床角度来看,检测到这种现象至关重要,因为腹泻是移植患者发病和死亡的重要原因,而这种疾病的治疗与其他腹泻原因的治疗完全不同。氨基水杨酸酯类药物和皮质类固醇疗程提供了有效的治疗方法。

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