Persić M, Prica M, Rajh-Gustincić M, Sepić A, Sabolić J
Acta Med Iugosl. 1989;43(2):137-46.
The authors present 2 patients with cirrhosis of the liver associated with alpha-1-antitrypsin deficiency. The patients are two children (brother and sister aged 4 and 13). The manifestation of the disease in these two children was a prolonged neonatal icterus. The symptoms of a decompensated cirrhosis of the liver appeared at the age of 2 and 4 years. There were several attacks of obstructive bronchitis etiologically associated with the same cause. The boy died at the age of four of hepatic coma preceded by several bleedings from esophageal varices. Splenectomy was performed in the girl on account of distinct signs of hyperplenism and two and a half years later mesentericocaval shunt because of the extensive bleeding from esophageal varices and the fundus of the stomach. The diagnosis of alpha-1-antitrypsin deficiency was made on the basis of low values in the serum and on the basis of liver biopsö and findings of typical PAS positive inclusions in the endoplasmic reticulum of hepatocytes. The values of A1A parents are also lower. The finding of Pi phenotypification is significant--the SZ phenotype was found in two patients (brother and sister), which is seldom described in patients with cirrhosis of the liver.
作者报告了2例与α-1抗胰蛋白酶缺乏相关的肝硬化患者。这两名患者是儿童(兄妹,分别为4岁和13岁)。这两名儿童的疾病表现为新生儿黄疸持续时间延长。肝失代偿的症状分别出现在2岁和4岁时。有几次阻塞性支气管炎发作,病因相同。男孩在4岁时死于肝昏迷,之前有几次食管静脉曲张出血。女孩因明显的脾功能亢进体征接受了脾切除术,两年半后因食管静脉曲张和胃底大量出血接受了肠系膜上静脉-腔静脉分流术。α-1抗胰蛋白酶缺乏症的诊断基于血清值低以及肝活检和肝细胞内质网中典型的PAS阳性包涵体的发现。父母的A1A值也较低。Pi表型分型的结果很重要——两名患者(兄妹)均为SZ表型,这在肝硬化患者中很少见。