Traulsen J B
Odense Universitetshospital, dermatologisk afdeling.
Ugeskr Laeger. 1994 Mar 7;156(10):1474-5.
Genetically determined deficiency of alpha-1-antitrypsin, the primary serum protease inhibitor, can result in pulmonary emphysema or liver cirrhosis, and panniculitis may be an early symptom. A case of recurring panniculitis in a 29 year-old woman is described, which led to the diagnosis of severe alpha-1-antitrypsin deficiency (Pi ZZ). Serum alpha-1-antitrypsin levels should be measured in patients presenting with panniculitis.
基因决定的α-1抗胰蛋白酶(主要的血清蛋白酶抑制剂)缺乏可导致肺气肿或肝硬化,脂膜炎可能是早期症状。本文描述了一名29岁女性复发性脂膜炎病例,该病例最终诊断为严重的α-1抗胰蛋白酶缺乏(Pi ZZ型)。对于出现脂膜炎的患者,应检测其血清α-1抗胰蛋白酶水平。