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评估炎症性肠病中硫唑嘌呤治疗相关的非肝硬化性门静脉高压症。

Assessment of non-cirrhotic portal hypertension associated with thiopurine therapy in inflammatory bowel disease.

机构信息

University of Chicago, Section of Gastroenterology, Hepatology and Nutrition, Chicago, IL 60637, USA.

出版信息

J Crohns Colitis. 2011 Feb;5(1):48-53. doi: 10.1016/j.crohns.2010.08.007. Epub 2010 Oct 18.

Abstract

Thiopurines represent an effective and widely used immunosuppressant in the therapeutic armamentarium of inflammatory bowel disease. However up to 25% of patients may be unable to continue the drug due to side effects. The incidence of hepatotoxicity associated with thiopurine use is reported between 0% and 32%. Veno-occlusive disease, peliosis hepatis, perisinusoidal fibrosis and nodular regenerative hyperplasia have all been described with thiopurines. Recent trials of 6-tioguanine, although successful in patients with allergies to azathioprine or mercaptopurine, have been compromised by increased hepatotoxicity, either veno-occlusive disease or nodular regenerative hyperplasia. We describe a report of nodular regenerative hyperplasia in a Crohn's disease patient associated with 6-mercaptopurine therapy and have reviewed the management and the literature regarding this complication. Our report strengthens the importance of further safety studies to evaluate the etiology, prevalence, risk factors and screening modalities for hepatotoxicity, in particular of nodular regenerative hyperplasia, in patients treated with thiopurines for inflammatory bowel disease.

摘要

硫唑嘌呤是炎症性肠病治疗药物中的一种有效且广泛应用的免疫抑制剂。然而,多达 25%的患者可能由于副作用而无法继续使用该药物。据报道,使用硫唑嘌呤相关的肝毒性发生率在 0%至 32%之间。静脉闭塞性疾病、肝血窦扩张症、窦周纤维化和结节性再生性增生都与硫唑嘌呤有关。尽管 6-硫鸟嘌呤在对巯嘌呤或巯基嘌呤过敏的患者中取得了成功,但由于肝毒性(静脉闭塞性疾病或结节性再生性增生)增加,最近的试验受到了影响。我们描述了一例与 6-巯基嘌呤治疗相关的克罗恩病患者的结节性再生性增生病例,并回顾了关于这种并发症的治疗和文献。我们的报告强调了进一步进行安全性研究的重要性,以评估病因、流行率、危险因素和筛查方法,特别是在使用硫唑嘌呤治疗炎症性肠病的患者中,评估肝毒性,特别是结节性再生性增生的风险。

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