Mellado M J, Jara P, Valverde F, Díaz M C, Fuentes E, Larrauri J, Vázquez C
An Esp Pediatr. 1986 Jul;25(1):5-12.
Fourteen cases of alpha-1-antitrypsin deficiency are presented. All of them had a PIZZ phenotype except two in which a PIMZ phenotype was found. It must be pointed out that histological findings show a great variability among the different patients most of which did not have intracellular PAS-positive amylase inclusions in liver biopsy specimens. Clinical course did not correlate with either the age of onset of the disease or the phenotype found, thus indicating that other additional factors are involved in determining prognosis. We insist on the importance of a careful study of all neonatal hepatitis syndromes in order to rule out a alpha-1-antitrypsin deficiency.
本文报告了14例α-1抗胰蛋白酶缺乏症患者。除2例为PIMZ表型外,其余均为PIZZ表型。必须指出的是,组织学检查结果显示,不同患者之间存在很大差异,大多数患者的肝活检标本中没有细胞内PAS阳性淀粉酶包涵体。临床病程与疾病的发病年龄或所发现的表型均无关联,这表明在决定预后方面还涉及其他因素。我们强调仔细研究所有新生儿肝炎综合征以排除α-1抗胰蛋白酶缺乏症的重要性。