Rotor 氏综合征系少见病例,作者曾见1例,现摘要报告如下:患者徐×,男,21岁,某工厂工人,住院号68407,因巩膜、皮肤黄染多年在外院诊断为慢性肝炎于1980年10月18日住入本院。患者诉自幼尿色深如浓茶,皮肤较一般人为黄,但有时较深,有时较浅,颜色加深时不伴有发热及消化道症状,饮食和体力均正常,屡次查肝功 Rotor’s syndrome is a rare case, the authors have seen 1 case, the summary report is as follows: Patient Xu ×, male, 21 years old, a factory worker, hospital number 68407, due to the sclera, yellow skin dye for many years outside the hospital diagnosed with chronic hepatitis October 18, 1980 admitted to this hospital. Patients complained of urine urine as dark as tea, the skin than the average man-made yellow, but sometimes deeper, sometimes lighter, darker when the color is not accompanied by fever and gastrointestinal symptoms, diet and physical strength are normal, repeatedly check liver function