新生儿先天性胆道闭锁-喂120 我要健康网 不断地搔抓可使患部皮肤变厚，变厚的皮损又加重了瘙痒，形成愈痒愈抓，愈抓愈痒的恶性循环。 胆道闭锁 胆道闭锁(biliary atresia，BA)是新生儿期一种少见的严重黄疸性疾病，但却是新生儿梗阻性黄疸时需要外科处理的主要问题。胆道闭锁并非少见
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congenital biliary atresia 先天性胆道闭锁 ; 胆道闭锁 ; 第三节 ; 后天性胆道闭锁
extrahepatic biliary atresia [内科] 肝外胆管闭锁 ; 肝外胆道闭锁 ; 闭锁 ; 先天性胆道闭锁
intrahepatic biliary atresia 肝内胆管闭锁 ; 称肝内胆管闭锁
congenital biliary atresia of newborn 先天性胆管闭锁
neonatal biliary atresia 新生儿胆道闭锁
extrehe-patic biliary atresia 与肝外胆道闭锁
Latest Progress of Biliary Atresia 胆道闭锁最新进展
Backgrounds:Infantile obstructive jaundice (OJ),a common symptom of congenital biliary atresia,biliary dilatation,and biliary dysplasia, often associates with systemic and local immune dysfunction,malnutrition,gut barrier dysfunction.
研究背景：小儿梗阻性黄疸(obstructive jaundice，OJ)见于先天性胆道闭锁、胆管扩张症、胆管发育不良等疾病，常伴有全身和局部免疫功能异常、营养不良和肠屏障功能障碍，进而引起肠道细菌和内毒素移位、肠源性感染和多系统器官损害。
参考来源 - 肠内营养和黄芪对梗阻性黄疸幼鼠肠屏障和肝脏损害的保护作用·2,447,543篇论文数据，部分数据来源于NoteExpress
In children, the most common reason for liver transplantation is biliary atresia.
在儿童肝脏移植最常见的原因是胆道闭锁。
Seen here is the major differential diagnosis of biliary atresia: this is neonatal giant cell hepatitis.
此图为胆道闭锁的主要不同诊断：这是一例新生儿巨细胞肝炎。
The pathology of liver was studied in 14 patients with congenial biliary atresia after Kasai's operation.
对14例胆道闭锁患儿进行葛西手术后肝脏病理变化的研究。
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