Rare clinical case: Autoimmune hepatitis type 3

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Autoimmune hepatitis

Autoimmune hepatitis is (AIH) is a chronic hepatitis that occurs in children and adults of all ages. It is characterized by immunologic and autoimmune features, including circulating auto antibodies and high serum globulin concentrations. It was first described in the 1950s by term of chronic active hepatitis. It has 2 types with different auto antibodies. Diagnosis is based upon serologic and ...

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Autoimmune hepatitis: clinical challenges.

Waldenström first described the disease entity now termed autoimmune hepatitis (AIH) in 1950, when he observed a chronic form of hepatitis in young women.1 This hepatitis led to cirrhosis and was associated with jaundice, elevated gamma globulins, and amenorrhea.2 The disease was found to be associated with other autoimmune syndromes3 and was later termed “lupoid hepatitis” because of the prese...

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Autoimmune hepatitis (AIH) is a progressive, chronic liver disease characterized by unresolving hepatocellular inflammation of autoimmune origin. The clinical spectrum may vary from asymptomatic presentation, to non-specific symptoms such as fatigue, arthralgias, nausea and abdominal pain, to acute severe liver disease. AIH is characterized by the presence of interface hepatitis and portal plas...

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Type 2 autoimmune hepatitis and hepatitis C virus infection.

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Autoimmune hepatitis (AIH) is an uncommon cause of severe chronic hepatitis with a female predilection and affecting all ages and ethnic groups. Although its pathogenesis is still not completely clear, the condition has been linked to dysimmunoregulation of T lymphocytes, which attack and damage the hepatic parenchyma. Characteristic autoantibodies are produced against hepatocytes leading to ce...

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ژورنال

عنوان ژورنال: Experimental and Clinical Gastroenterology

سال: 2020

ISSN: 1682-8658

DOI: 10.31146/1682-8658-ecg-177-5-120-126