Varma R R, Grainger J M, Scheuer P J
Gut. 1970 Oct;11(10):817-21. doi: 10.1136/gut.11.10.817.
A patient is described in whom the Dubin-Johnson syndrome was diagnosed after an attack of acute hepatitis at the age of 21. In the eight years following the hepatitis Dubin-Johnson pigment, initially scanty, developed to classical proportions. The defect in intracellular transport of bilirubin was thought to precede the attack of acute hepatitis.
本文描述了一名患者，该患者在21岁时患急性肝炎后被诊断为杜宾-约翰逊综合征。肝炎后的八年里，起初数量稀少的杜宾-约翰逊色素发展到典型比例。胆红素细胞内转运缺陷被认为在急性肝炎发作之前就已存在。
