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Gilbert 病又称慢性间歇性幼年性黄疸,是一种罕见的良性家族性非结合性高胆红素血症。此病往往易被误诊为其他肝胆疾病而手术或受长期药物治疗,给病人造成不应有的痛苦。因此,本病在黄疸的鉴别诊断中有着重要的意义。我院见到一例,报告如下。男性,16岁,学生。因巩膜及全身皮肤持续性发黄10年,近来因倦怠、乏力,于80年8月25日住院。患者6岁时因啼哭,泪呈黄色而引起注意,并发现眼球亦发黄,因此曾住某医院按“肝炎”治疗两个月,无效而出院。此后一直未到医院检查过,但黄疸一直持续存在,时轻时重。平日不喜欢活动,较馋懒。有时自
Gilbert disease, also known as chronic intermittent juvenile jaundice, is a rare benign familial non-conjugated hyperbilirubinemia. The disease is often easily misdiagnosed as other liver and gallbladder disease surgery or long-term drug treatment, causing undue suffering to the patient. Therefore, the disease in the differential diagnosis of jaundice has an important significance. I saw a hospital, the report is as follows. Male, 16 years old, student. Due to persistent scleral and systemic skin yellowing 10 years, recently due to fatigue, fatigue, in August 80, 80 hospitalized. At 6 years of age, he was crying and tears were yellow. He also noticed yellowing of the eyeball. He was hospitalized for two months according to “Hepatitis” and was discharged ineffectively. Has not been to the hospital since then, but jaundice has persisted, when light weight. Weekdays do not like activities, more lazy. Sometimes