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甲氨蝶呤/萘普生引发的一名幼年特发性关节炎患儿的严重肝炎

Methotrexate/naproxen-associated severe hepatitis in a child with juvenile idiopathic arthritis.

作者信息

Ting T V, Hashkes P J

机构信息

Section of Pediatric Rheumatology, Department of Rheumatic Diseases, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.

出版信息

Clin Exp Rheumatol. 2007 Nov-Dec;25(6):928-9.

Abstract

Methotrexate (MTX) is a cornerstone in the treatment of juvenile idiopathic arthritis (JIA). Although associated with many mild adverse effects, the short and long-term safety of MTX in JIA has been excellent. While many JIA children treated with MTX develop liver enzyme abnormalities, no cases of irreversible liver damage or of severe non-infectious hepatitis with Reye-like features have been reported in non-systemic JIA. We report a 2-year-old girl with oligoarthritis whose liver enzyme increased to greater than 45 times the upper limit of normal, and developed hypoglycemia and hyperammonemia after 10 months of MTX and naproxen therapy. An infectious and metabolic work-up for other causes was unremarkable. She recovered completely after folinic acid therapy; MTX and naproxen was not restarted. While very rare in JIA, MTX in synergism with naproxen can induce severe liver toxicity and it is important to screen children for liver enzyme abnormalities.

摘要

甲氨蝶呤(MTX)是治疗幼年特发性关节炎(JIA)的基石。尽管它会引发许多轻微的不良反应,但MTX在JIA治疗中的短期和长期安全性一直良好。虽然许多接受MTX治疗的JIA患儿会出现肝酶异常,但在非系统性JIA中,尚未有不可逆肝损伤或具有瑞氏样特征的严重非感染性肝炎的病例报告。我们报告了一名患有少关节炎的2岁女孩,在接受MTX和萘普生治疗10个月后,其肝酶升高至正常上限的45倍以上,并出现低血糖和高氨血症。针对其他病因的感染和代谢检查结果无异常。她在接受亚叶酸治疗后完全康复;未重新使用MTX和萘普生。虽然在JIA中非常罕见,但MTX与萘普生协同作用可诱发严重的肝毒性,因此对儿童进行肝酶异常筛查很重要。

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