Keim H J, Farack U M, Gabbert H
Leber Magen Darm. 1979 Sep;9(5):272-6.
It is well known that incidence of chronic obstructive lung disease in adult patients with alpha 1-antitrypsin deficiency (ATD) is high. Adult carriers of this genetic trait with cirrhosis of the liver, and also with fibrosis of the liver and hepatoma, have been reported. A causal relationship between ATD and liver lesions has been suspected. In most cases liver disease has been recognized at post morten, - in a few cases, however, intra vitam, when severe symptoms of the liver disease had become apparent. The case of a 59 year-old patient is reported with PIZZ-homozygous ATD, moderate pulmonary emphysema and with marked portal fibrosis and focal transition in cirrhosis of the liver without any sequelae. The clinical course has been rather benign so far.
众所周知,α1 -抗胰蛋白酶缺乏症(ATD)成年患者中慢性阻塞性肺疾病的发病率很高。有报道称,携带这种遗传特征的成年人会出现肝硬化,以及肝纤维化和肝癌。人们怀疑ATD与肝脏病变之间存在因果关系。在大多数情况下,肝脏疾病是在尸检时才被发现的——然而,在少数情况下,是在出现严重肝病症状时在生前被发现的。本文报道了一例59岁的患者,该患者为PIZZ纯合子ATD,患有中度肺气肿,伴有明显的门静脉纤维化和肝硬化的局灶性转变,但无任何后遗症。到目前为止,临床病程相当良性。