医学
全血细胞减少症
再生障碍性贫血
肝损伤
肝活检
肝炎
骨髓
免疫学
胃肠病学
阵发性夜间血红蛋白尿
药品
贫血
内科学
活检
药理学
作者
Jun Nagai,Toshihiro Matsukawa,Keito Suto,Kazuo Oshimi,Takuto Miyagishima
出处
期刊:PubMed
日期:2019-01-01
卷期号:60 (7): 779-784
标识
DOI:10.11406/rinketsu.60.779
摘要
Aplastic anemia (AA), a hematopoietic disorder characterized by hypocellular bone marrow, is caused by immunologically-mediated hematopoietic stem cell injury. Viral infection is hypothesized as the underlying cause of hepatitis-associated AA, although its mechanism is still unclear. This report describes a case of AA following suspected drug-induced liver injury (DILI). An 18-year-old man developed severe liver dysfunction after taking oral over-the-counter drugs. The patient was diagnosed with suspected DILI based on drug-induced lymphocyte stimulation test and liver biopsy results. Although liver dysfunction improved after a course of steroid pulse therapy and liver supporting therapy, the man gradually developed pancytopenia within 3 months of DILI diagnosis, prompting the diagnosis of AA following DILI. Paroxysmal nocturnal hemoglobinuria-type cells were detected by high-sensitivity flow cytometry. Immunosuppressive therapy with antithymocyte globulin and cyclosporin was administered, with pancytopenia improvement. To the best of our knowledge, this is the first report in the literature with a case of AA following DILI, and we believe it is important for evaluating the pathogenesis of drug-induced and hepatitis-associated AA.
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