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美泊利珠单抗治疗嗜酸性肉芽肿性血管炎致肝损伤1例报告

Liver injury induced by mepolizumab in treatment of eosinophilic granulomatosis with polyangiitis: a case report

  • 摘要: 1例52岁女性患者,诊断为嗜酸性肉芽肿性血管炎(eosinophilic granulomatosis with polyangiitis, EGPA)、哮喘、过敏性鼻炎,行美泊利珠单抗(100 mg,4周1次)治疗。第2次给药后3 d出现尿液黄染,给药后6 d发现肝功能指标异常:总胆红素(total bilirubin, TBIL)22 μmol/L,直接胆红素(direct bilirubin, DBIL)14.9 μmol/L,丙氨酸氨基转移酶(alanine aminotransferase, ALT)461 U/L,天冬氨酸氨基转移酶(aspartate aminotransferase, AST)129 U/L,碱性磷酸酶(alkaline phosphatase, ALP)296 U/L。综合评估后,考虑该患者为美泊利珠单抗致药物性肝损伤,给予异甘草酸镁、谷胱甘肽和熊去氧胆酸保肝治疗。治疗5 d后,患者尿液颜色变浅,肝功能指标改善:TBIL 17.4 μmol/L,DBIL 9.8 μmol/L,ALT 214 U/L,AST 85 U/L,ALP 226 U/L。继续保肝治疗约2周后,患者肝功能恢复正常。随后暂停美泊利珠单抗治疗,并持续随访约半年,患者未再出现肝功能异常及其他不适。

     

    Abstract: A 52-year-old female patient was diagnosed with eosinophilic granulomatosis with polyangiitis (EGPA), asthma and allergic rhinitis and was treated with mepolizumab (100 mg, once every 4 weeks). Three days after the second administration, the patient developed dark yellow urine, and abnormal liver function indicators were found on day 6 after administration. Laboratory tests showed total bilirubin (TBIL) of 22 μmol/L, direct bilirubin (DBIL) of 14.9 μmol/L, alanine aminotransferase (ALT) of 461 U/L, aspartate aminotransferase (AST) of 129 U/L, and alkaline phosphatase (ALP) of 296 U/L. After comprehensive assessment, it was considered that mepolizumab caused drug-induced liver injury in the patient. Magnesium isoglycyrrhizinate, glutathione, and ursodeoxycholic acid were used for liver protection. Five days later, the urine color became lighter and liver function indicators improved (TBIL 17.4 μmol/L, DBIL 9.8 μmol/L, ALT 214 U/L, AST 85 U/L, ALP 226 U/L). After about 2 weeks of continued liver protection treatment, liver function returned to normal. Mepolizumab treatment was suspended and during the follow-up for about half one year, the patient did not experience liver function abnormalities or other discomforts again.

     

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