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Gilbtrt氏病也称先天性非溶血性黄疸(间接胆红质增高型),或体质性肝功不良性黄疸。属于先天佳胆红质代谢功能缺陷,易被误诊为慢性肝炎或胆囊炎而长期误治。现介绍我院收治一例如下。 【病例】男性,25岁。因巩膜皮肤间歇黄染20余年而入院。病人于3岁时患“急性黄疸型肝炎”。收某医院住院治疗,治愈出院。于8岁左右发现巩膜黄染,但无何不适症状,以后黄疸间歇出现。多次检查
Gilbtrt’s disease is also called congenital non-hemolytic jaundice (indirect hypercholesterolemia), or constitutional liver dysfunction jaundice. Belongs to congenital sweet bile metabolism defects, easily misdiagnosed as chronic hepatitis or cholecystitis and long-term misdiagnosis. Now introduce a hospital in our hospital as follows. [Case] Male, 25 years old. Intermittent scleral skin yellow dye for more than 20 years and admission. The patient had “acute jaundice hepatitis” at the age of 3 years. Receive a hospital for treatment, cured and discharged. Found in the 8-year-old scleral yellow dye, but no symptoms, after intermittent jaundice. Check multiple times