Ghishan F K, Gray G F, Greene H L
Gastroenterology. 1983 Aug;85(2):435-8.
We report a 2-wk-old baby with alpha 1-antitrypsin deficiency of Pizz phenotype, who presented with massive ascites and hepatomegaly. Liver biopsy disclosed active established cirrhosis. Unlike all other reported newborns with Pizz type, the patient had no evidence of neonatal cholestatic jaundice. The presentation of Pizz with established liver cirrhosis at such an early age not only adds another cause of cryptogenic cirrhosis in the neonatal period, but also points to a liver insult in some patients with Pizz, which is already determined in utero.
我们报告了一名2周大患有Pizz表型α1-抗胰蛋白酶缺乏症的婴儿,该婴儿出现大量腹水和肝肿大。肝活检显示为活动性肝硬化。与所有其他报道的Pizz型新生儿不同,该患者没有新生儿胆汁淤积性黄疸的证据。Pizz型在如此早期就出现肝硬化,这不仅增加了新生儿期隐源性肝硬化的另一个病因,也表明部分Pizz患者在子宫内就已受到肝脏损伤。