Autoimmune hepatitis: Unveiling faces

被引：6

作者：

Zhu, Jiang Yi ^{[1
]}

Han, Ying ^{[1
]}

机构：

[1] Fourth Mil Med Univ, Xijing Hosp, Dept Gastroenterol, Xian 710032, Shaanxi, Peoples R China

来源：

JOURNAL OF DIGESTIVE DISEASES | 2015年 / 16卷 / 09期

关键词：

autoantibody; diagnosis; hepatitis; autoimmune; treatment; T-CELLS; LIVER-DISEASE; JAPANESE PATIENTS; TYPE-1; EPIDEMIOLOGY; PATHOGENESIS; DIAGNOSIS; POPULATION; MANAGEMENT; REMISSION;

D O I：

10.1111/1751-2980.12285

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

Autoimmune hepatitis (AIH) is a complex multifactorial liver disease with unknown etiology. It may be induced by certain triggers that cause immune disorders and autoimmune attack in genetically susceptible individuals, which ultimately results in chronic persistent interface inflammation of the liver. The diagnosis of AIH is made based on comprehensive evaluation score system. All AIH patients should receive interventions and the mainstay therapy is prednisone alone or in combination with azathioprine. Further exploratory researches on refractory AIH have been developed. Liver transplantation is still the only effective option for patients with decompensated cirrhosis or hepatic failure.

引用

页码：483 / 488

页数：6

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