Battle W M, Matarazzo S A, Selhat G F, Catalano E
J Clin Gastroenterol. 1982 Jun;4(3):269-73. doi: 10.1097/00004836-198206000-00014.
We report a 73-year-old woman with homozygous ZZ alpha-1-antitrypsin deficiency (AATD), micronodular cirrhosis, cholestatic jaundice, and emphysema. An elevated SGOT/SGPT ratio was noted in the absence of chronic alcoholism. ERCP demonstrated a normal extrahepatic biliary system and suggested obstruction of the intrahepatic ducts. An operative liver biopsy demonstrated periodic acid-Schiff-positive, diastase resistant intracytoplasmic inclusion bodies. This patient reminds us that metabolic causes of cryptogenic liver disease need to be considered, even in the elderly. We review briefly the literature concerning AATD and liver disease.
我们报告了一名73岁的女性,她患有纯合子ZZα-1抗胰蛋白酶缺乏症(AATD)、小结节性肝硬化、胆汁淤积性黄疸和肺气肿。在无慢性酒精中毒的情况下,发现谷草转氨酶/谷丙转氨酶比值升高。内镜逆行胰胆管造影(ERCP)显示肝外胆管系统正常,并提示肝内胆管梗阻。手术肝活检显示高碘酸-希夫染色阳性、淀粉酶抵抗性胞浆内包涵体。该患者提醒我们,即使是老年人,也需要考虑隐源性肝病的代谢原因。我们简要回顾了有关AATD和肝病的文献。