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肝外胆道闭锁、特发性新生儿肝炎和α-1抗胰蛋白酶缺乏症(PiZ)患者的血清甲胎蛋白水平

Serum alpha-fetoprotein levels in extrahepatic biliary atresia, idiopathic neonatal hepatitis and alpha-1-antitrypsin deficiency (PiZ).

作者信息

Johnston D I, Mowat A P, Orr H, Kohn J

出版信息

Acta Paediatr Scand. 1976 Sep;65(5):623-9. doi: 10.1111/j.1651-2227.1976.tb04942.x.

Abstract

Serum alpha-fetoprotein levels were measured using a sensitive radioimmunoassay in 77 infants presenting with persistent conjugated hyperbilirubinaemia. A breed range of alpha-fetoprotein concentrations occurred in both the 23 infants with extrahepatic biliary atresia and the 35 with idiopathic neonatal hepatitis but the 13 with alpha-1-antitrypsin deficiency had uniformly low levels. High alpha-fetoprotein concentrations (above 10 000 mug/1) favoured the diagnosis of neonatal hepatitis especially in the first ten weeks of life, but the overlap between neonatal hepatitis and extrahepatic biliary atresia was large and alpha-fetoprotein determination cannot be recommended as a reliable method for distinguishing the two conditions. Serial alpha-fetoprotein values showed no consistent relationship with standard liver function tests and gave no guide to prognosis. There was an association between alpha-fetoprotein production and needle biopsy evidence of hepatic giant cell transformation. The uniformly low alpha-fetoprotein levels in alpha-1-antitrypsin deficient infants with neonatal hepatitis is a new observation and possible mechanisms for disordered glycoprotein release are discussed.

摘要

采用灵敏的放射免疫分析法对77例持续性结合胆红素血症婴儿测定血清甲胎蛋白水平。肝外胆道闭锁的23例婴儿和特发性新生儿肝炎的35例婴儿甲胎蛋白浓度有一定范围,但13例α1抗胰蛋白酶缺乏症婴儿的甲胎蛋白水平均较低。甲胎蛋白浓度高(超过10000μg/1)有助于新生儿肝炎的诊断,尤其是在出生后的头十周,但新生儿肝炎和肝外胆道闭锁之间的重叠范围很大,因此不推荐将甲胎蛋白测定作为区分这两种疾病的可靠方法。连续的甲胎蛋白值与标准肝功能试验无一致关系,也不能作为预后的指标。甲胎蛋白产生与肝巨细胞转化的肝穿刺活检证据之间存在关联。α1抗胰蛋白酶缺乏症新生儿肝炎婴儿甲胎蛋白水平均较低是一项新的观察结果,并讨论了糖蛋白释放紊乱的可能机制。

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