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儿童患者的急性肝炎:免疫介导的药物性肝损伤还是阿苯达唑诱导的自身免疫性肝炎?

Acute hepatitis in a paediatric patient: immune-mediated drug-induced liver injury or albendazole-induced autoimmune hepatitis?

机构信息

Department of Gastroenterology, University Children's Hospital, Belgrade, Serbia.

Clinic for Infectious and Tropical Diseases, Clinical Center of Serbia, Belgrade, Serbia.

出版信息

J Infect Dev Ctries. 2022 Oct 31;16(10):1660-1663. doi: 10.3855/jidc.16594.

Abstract

INTRODUCTION

Drug-induced liver injury (DILI) is one of the most common causes of liver damage. A large number of drugs, dietary supplements, and herbal medications can cause hepatotoxicity. In some situations, it is difficult to distinguish between DILI and autoimmune hepatitis, especially when the mechanism is immune-mediated. Albendazole is a drug that has been used for decades for the treatment of parasitic infections in humans. One of the side effects is liver enzyme elevation, but rarely requires the discontinuation of therapy. Previous experience has shown that hypersensitivity is the most common mechanism of albendazole hepatotoxicity.

CASE REPORT

Here we presented a paediatric patient in whom albendazole induced severe liver injury. In laboratory analyses, in addition to markedly elevated transaminases and parameters of cholestasis, there was also a significant increase in IgG, so autoimmune hepatitis was considered. Even though the liver histology indicated toxic liver disease, prednisolone was started. Corticosteroid therapy resulted in the complete normalization of liver function, as well as IgG. With the cessation of corticosteroid therapy, transaminases, bilirubin and gamma-glutamyl transferase (GGT) remained within normal levels, but an increase in anti-smooth muscle antibodies (SMA) was noted in immunological analyses after one year of follow-up.

CONCLUSIONS

Immune-mediated hepatotoxicity from albendazole is one possible mechanism of liver injury. The use of albendazole in the treatment of parasitic infections, especially in children, requires close monitoring. The question remains as to whether albendazole is a drug that can induce autoimmune hepatitis in the paediatric population.

摘要

简介

药物性肝损伤(DILI)是肝损伤的最常见原因之一。大量的药物、膳食补充剂和草药都可能导致肝毒性。在某些情况下,很难将 DILI 与自身免疫性肝炎区分开来,尤其是当机制是免疫介导的时。阿苯达唑是一种已使用数十年的药物,用于治疗人类寄生虫感染。其副作用之一是肝酶升高,但很少需要停止治疗。以往的经验表明,超敏反应是阿苯达唑肝毒性的最常见机制。

病例报告

在这里,我们介绍了一例阿苯达唑引起严重肝损伤的儿科患者。在实验室分析中,除了明显升高的转氨酶和胆汁淤积参数外,IgG 也显著升高,因此考虑自身免疫性肝炎。尽管肝组织学提示为中毒性肝病,但开始使用泼尼松龙。皮质类固醇治疗导致肝功能和 IgG 完全正常化。停用皮质类固醇后,转氨酶、胆红素和γ-谷氨酰转移酶(GGT)在随访 1 年后仍在正常范围内,但免疫分析显示抗平滑肌抗体(SMA)增加。

结论

阿苯达唑引起的免疫介导性肝毒性是肝损伤的一种可能机制。阿苯达唑在寄生虫感染的治疗中的应用,特别是在儿童中,需要密切监测。阿苯达唑是否是一种可在儿科人群中引起自身免疫性肝炎的药物仍存在疑问。

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