Lilly J R, Javitt N B
Ann Surg. 1976 Sep;184(3):369-75. doi: 10.1097/00000658-197609000-00014.
Since 1974, 16 consecutive infants with biliary atresia have been treated by hepatic portoenterostomy employing an exteriorized Roux-en-Y intestinal segment (Miluliez). Simultaneous, sequential analyses of bile pigments and lipids in serum and biliary drainage were performed. In the 11 patients with sustained bile drainage, progressive increases in bile volume, bilirubin and biliary lipid concentrations correlated well with their subsequent return toward normal in the serum. Despite relief of biliary obstruction, four patients have had progressive liver cirrhosis. The other 7 have residual liver damage which has been stable, or in two instances, improved, at late biopsy. The clinical and biochemical results suggest that both obstructive and parenchymal factors are operative in infants with biliary atresia.
自1974年以来,连续16例胆道闭锁婴儿接受了采用外置Roux-en-Y肠段(米吕列兹术)的肝门肠吻合术治疗。同时,对血清和胆汁引流中的胆色素和脂质进行了连续分析。在11例胆汁持续引流的患者中,胆汁量、胆红素和胆汁脂质浓度的逐渐增加与随后血清恢复正常密切相关。尽管胆道梗阻得到缓解,但仍有4例患者出现进行性肝硬化。另外7例有残余肝损伤,在后期活检时病情稳定,有2例有所改善。临床和生化结果表明,梗阻性和实质性因素在胆道闭锁婴儿中均起作用。