Horsmans Y, Rahier J, Geubel A P
Department of Gastroenterology, St-Luc University Hospital and Medical School (UCL), Brussels, Belgium.
Liver. 1991 Apr;11(2):89-93. doi: 10.1111/j.1600-0676.1991.tb00497.x.
A 67-year-old patient, with primary polymyositis and without previous evidence of liver disease, developed clinical and biochemical features of severe cholestasis 3 months after initiation of azathioprine therapy. Liver biopsy showed cholestasis with both cytological and architectural alterations of interlobular bile ducts. Azathioprine withdrawal resulted after 7 weeks in the resolution of clinical and biochemical abnormalities. It is believed that this is the first reported case of reversible azathioprine-induced cholestasis associated with histological evidence of bile duct injury.
一名67岁的患者,患有原发性多肌炎,既往无肝脏疾病证据,在开始硫唑嘌呤治疗3个月后出现了严重胆汁淤积的临床和生化特征。肝活检显示胆汁淤积,伴有小叶间胆管的细胞学和结构改变。停用硫唑嘌呤7周后,临床和生化异常得到缓解。据信,这是首例有可逆性硫唑嘌呤诱导的胆汁淤积且伴有胆管损伤组织学证据的报道病例。