Czaja Albert J, Carpenter Herschel A
Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, 200 First Street Southwest, Rochester, MN 55905, USA.
Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, 200 First Street Southwest, Rochester, MN 55905, USA.
Gastroenterol Clin North Am. 2017 Jun;46(2):345-364. doi: 10.1016/j.gtc.2017.01.008.
Autoimmune hepatitis (AIH) may have an atypical serum alkaline phosphatase elevation, antimitochondrial antibodies, histologic features of bile duct injury/loss, or cholangiographic findings of focal biliary strictures and dilations. These manifestations characterize the overlap syndromes. Patients can be classified as having AIH with features of primary biliary cholangitis, primary sclerosing cholangitis, or a cholestatic syndrome. The gold standard of diagnosis is clinical judgment. Histologic evaluation is a major diagnostic component. Treatment is based on algorithms; outcomes vary depending on the predominant disease component. Combination therapy has been the principal recommendation.
自身免疫性肝炎(AIH)可能出现非典型血清碱性磷酸酶升高、抗线粒体抗体、胆管损伤/缺失的组织学特征,或局灶性胆管狭窄和扩张的胆管造影表现。这些表现是重叠综合征的特征。患者可被分类为具有原发性胆汁性胆管炎、原发性硬化性胆管炎或胆汁淤积综合征特征的自身免疫性肝炎。诊断的金标准是临床判断。组织学评估是主要的诊断组成部分。治疗基于算法;结局因主要疾病成分而异。联合治疗一直是主要推荐方案。