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一位患有格雷夫斯病的年轻菲律宾女性出现甲巯咪唑诱发的再生障碍性贫血并伴有肝炎

Methimazole-Induced Aplastic Anemia with Concomitant Hepatitis in a Young Filipina with Graves' Disease.

作者信息

Wijaya Natalia, Ong-Ramos Celeste

机构信息

Department of Internal Medicine, De Los Santos Medical Center, Quezon City, Philippines.

出版信息

J ASEAN Fed Endocr Soc. 2019;34(1):99-102. doi: 10.15605/jafes.034.01.16. Epub 2019 May 21.

Abstract

A 34-year-old female Filipino with Graves' disease on methimazole came in due to fever, sore throat and jaundice. She was initially diagnosed with methimazole-induced agranulocytosis and drug-induced liver injury. She was treated with intravenous broad-spectrum antibiotic and granulocyte colony stimulating factor. On day 4 of admission, she developed pancytopenia and was managed as methimazole-induced aplastic anemia. She was started on steroid therapy and received 1 unit of packed red blood cell. The jaundice also increased, hence, she was given ursodeoxycholic acid. On day 9 of admission, with the consideration of "lineage steal phenomenon," biopsy was done and eltrombopag was started. Patient was discharged stable at 12th hospital day. This case presents 3 rare life-threatening complications of methimazole namely: agranulocytosis, aplastic anemia and hepatitis.

摘要

一名34岁患格雷夫斯病且正在服用甲巯咪唑的菲律宾女性,因发热、咽痛和黄疸前来就诊。她最初被诊断为甲巯咪唑引起的粒细胞缺乏症和药物性肝损伤。她接受了静脉注射广谱抗生素和粒细胞集落刺激因子治疗。入院第4天,她出现全血细胞减少,并被诊断为甲巯咪唑引起的再生障碍性贫血。她开始接受类固醇治疗,并输注了1单位浓缩红细胞。黄疸也有所加重,因此,给她使用了熊去氧胆酸。入院第9天,考虑到“谱系窃取现象”,进行了活检并开始使用艾曲泊帕。患者在住院第12天病情稳定出院。该病例呈现了甲巯咪唑3种罕见的危及生命的并发症,即:粒细胞缺乏症、再生障碍性贫血和肝炎。

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