[α -1-抗胰蛋白酶缺乏引起的肝硬化]。

Acta medica Iugoslavica Pub Date : 1989-01-01
M Persić, M Prica, M Rajh-Gustincić, A Sepić, J Sabolić
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引用次数: 0

摘要

作者报告了2例肝硬化合并α -1-抗胰蛋白酶缺乏的患者。患者为两名儿童(分别为4岁和13岁的兄妹)。这两个孩子的疾病表现为新生儿黄疸延长。失代偿性肝硬化的症状出现在2岁和4岁。有几次发作的阻塞性支气管炎的病因与同一原因。这名男孩在四岁时死于肝昏迷,并伴有食管静脉曲张出血。由于有明显的脾功能亢进症状,并在两年半后因食管静脉曲张和胃底大量出血而行肠系膜-腔静脉分流术。α -1抗胰蛋白酶缺乏症的诊断是基于血清和肝脏biopsö的低值以及肝细胞内质网中典型PAS阳性包涵体的发现。A1A父母的值也较低。Pi表型的发现意义重大——在2例患者(兄弟和姐妹)中发现了SZ表型,这在肝硬化患者中很少被描述。
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[Liver cirrhosis caused by alpha-1-antitrypsin deficiency].

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.

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