医学
自身免疫性肝炎
肝病
脂肪肝
系统性红斑狼疮
肝炎
病毒性肝炎
痹症科
酒精性肝炎
黄疸
肝硬化
原发性胆汁性肝硬化
内科学
肝损伤
疾病
红斑狼疮
免疫学
胃肠病学
酒精性肝病
抗体
作者
Wais Afzal,Mehdi Haghi,SA Hasni,KA Newman
标识
DOI:10.1080/03009742.2020.1744712
摘要
Systemic lupus erythematosus (SLE), a multisystem autoimmune inflammatory disease, may involve any organs, including the liver. Liver involvement in SLE is not part of the American College of Rheumatology criteria and is relatively rare. Liver disease is usually mild, manifesting as subtle elevation of liver enzymes. Jaundice and hepatomegaly can be seen in some patients; advanced liver disease with cirrhosis is extremely rare. Precise pathology remains obscure. SLE may cause non-specific changes, including hepatocellular, cholestatic, or vascular changes. Alcohol, drugs, viral infections, metabolic disorders, autoimmune hepatitis, and other common causes of liver dysfunction should be excluded. Corticosteroids may expedite the recovery process, but may lead to non-alcoholic fatty liver disease and liver damage. Several large-scale multicentre studies have shown that liver involvement is not the major cause of morbidity and mortality in SLE patients. In this review, we discuss the pathogenesis, diagnosis, differential diagnosis, clinical manifestations, management, complications, and prognosis of lupus hepatitis.
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