慢性间歇性幼年性黄疸即Gilbert氏病。系因肝细胞从血液中摄取胆红素能力减退而致的一种先天性高胆红素血症,常易误诊。病例摘要患者男,38岁,1973年5月6日初诊。诉:自10岁前后即发现巩膜黄染间歇性加重,持续不退,无不适感觉。1964年一度黄疸加重,在某院诊断为“黄疸型肝炎”、“胆囊炎”、“梗阻性黄疸”。近年来黄疸常因劳累及熬夜后加重,但能担负日常工作。尿量少时尿色可变深。未发现大便颜色变浅;无腹痛、搔痒、恶心、厌油等情况。 Chronic intermittent juvenile jaundice is Gilbert’s disease. Department of liver cells from the blood intake of bilirubin caused by a congenital hyperbilirubinemia, often misdiagnosed. Case Summary Male patient, 38 years old, May 6, 1973 First visit. V. Since the age of 10 found that intermittent episodes of scleral yellow dye, continuous, no discomfort. Jaundice was first aggravated in 1964, in a hospital diagnosed as “jaundice hepatitis”, “cholecystitis”, “obstructive jaundice.” In recent years, jaundice often aggravated by overwork and staying up late, but can take on day-to-day work. Urine may be darker when urine is darker. No stool color was found lighter; no abdominal pain, itching, nausea, tired of oil and so on.