Deutsch J, Smith A L, Danks D M, Campbell P E
Arch Dis Child. 1985 May;60(5):447-51. doi: 10.1136/adc.60.5.447.
A total of 123 patients with neonatal liver disease without extrahepatic bile duct obstruction or arteriohepatic dysplasia have been studied for six to 18 years. Idiopathic neonatal hepatitis, present in 73 babies, carried a high mortality due to liver failure (18%), septicaemia (6%), and associated defects (14%), especially in the first year of life (25%). Progression to chronic liver disease in non-familial idiopathic cases occurred in three of 40 reviewed patients. Only 12 of these children were completely healthy, the remainder having other permanent disabilities (57%). Four of nine familial cases of idiopathic neonatal hepatitis died in the first 12 months of life as did two of the four reviewed survivors. Progression to chronic liver disease or to death was a continuous process without any interval of recovery in all but one of these patients. Among patients with a presumed infective cause, cytomegalovirus infection caused a particularly benign form of neonatal hepatitis but was a frequent cause of brain damage or other disabilities. Babies who survived other infective liver diseases showed complete healing of the liver damage. Neonatal liver disease associated with alpha 1 antitrypsin deficiency progressed to death or chronic liver disease in three of nine patients and was not associated with a paucity of interlobular bile ducts.
对123例无肝外胆管梗阻或动脉肝发育不良的新生儿肝病患者进行了6至18年的研究。73例婴儿患有特发性新生儿肝炎,因肝衰竭(18%)、败血症(6%)及相关缺陷(14%)导致的死亡率很高,尤其是在生命的第一年(25%)。在40例接受复查的非家族性特发性病例中,有3例进展为慢性肝病。这些儿童中只有12例完全健康,其余儿童有其他永久性残疾(57%)。9例家族性特发性新生儿肝炎病例中有4例在出生后的前12个月死亡,4例接受复查的幸存者中有2例也是如此。除1例患者外,所有这些患者进展为慢性肝病或死亡均为一个持续的过程,无任何恢复间隔。在推测有感染病因的患者中,巨细胞病毒感染导致一种特别良性的新生儿肝炎形式,但却是脑损伤或其他残疾的常见原因。在其他感染性肝病中存活下来的婴儿肝脏损伤完全愈合。与α1抗胰蛋白酶缺乏相关的新生儿肝病在9例患者中有3例进展为死亡或慢性肝病,且与小叶间胆管稀少无关。