慢性特发性黄疸,又称Dubin-Johnson二氏综合征,是一种罕见的先天性非溶血性黄疸,我们最近确诊一例,兹报告如下: 患者女性,23岁,河南籍,汉族,未婚,××车辆段工人,住院号51773。患者两年来因长期巩膜黄染,前后三次住院治疗。第一次于1978年12月13日拟诊“急性黄疸型肝炎”入院,经治疗消化道症状减轻,但黄疸未完全退尽而出院。第二次于1979年12月1日拟诊“黄疸待查”入院,本次伴有发烧,经治疗好转,但黄疸亦未完全消退,出院诊断为“肝炎后直接胆红素增高血症”。第三次又因上述症状加重,于1980年10月8日入院,始 Chronic idiopathic jaundice, also known as Dubin-Johnson’s syndrome, is a rare congenital non-hemolytic jaundice. We recently reported a case as follows: Female, 23, Henan, Han, × × depot workers, hospital number 51773. Patients for two years due to long-term scleral yellow dye, before and after three hospitalizations. The first time in December 13, 1978 to be diagnosed “acute jaundice hepatitis” admitted to the treatment of gastrointestinal symptoms, but not completely discharged jaundice and discharged. The second time in December 1, 1979 to be diagnosed “jaundice pending” admission, this time with fever, the treatment improved, but jaundice has not completely dissipated, discharged diagnosed as “hepatitis bilirubin hypercapnia” . The third time because of the above symptoms worsened, on October 8, 1980 admission, beginning