Imaging of autoimmune hepatitis and overlap syndromes

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Autoimmune hepatitis (AIH) is an uncommon, chronic inflammatory, and relapsing liver disease of unknown origin that may lead to liver cirrhosis, hepatocellular carcinoma, liver transplantation, or death. AIH occurs in all age groups and races but can frequently manifest as acute fulminant hepatitis. Clinical presentation of AIH can have features similar to primary sclerosing cholangitis (PSC) and primary biliary cirrhosis (PBC), and these diseases may coexist leading to overlap syndromes. Although histological diagnosis is necessary, imaging features often can demonstrate characteristics that may be helpful to distinguish these diseases. Imaging features of AIH are those of chronic liver disease, and imaging plays important role in detection of complications and ruling out other possible causes of chronic liver disease. Emerging techniques such as elastography provide non-invasive options for diagnosis of significant fibrosis and cirrhosis during clinical follow-up as well as assessment of response to treatment. In this study, we will describe imaging findings in AIH and overlap syndromes.

Original languageEnglish (US)
Pages (from-to)19-27
Number of pages9
JournalAbdominal Radiology
Volume42
Issue number1
DOIs
StatePublished - Jan 1 2017

Fingerprint

Autoimmune Hepatitis
Liver Diseases
Fibrosis
Chronic Disease
Elasticity Imaging Techniques
Sclerosing Cholangitis
Biliary Liver Cirrhosis
Liver Cirrhosis
Liver Transplantation
Hepatitis
Hepatocellular Carcinoma
Age Groups

Keywords

  • Autoimmune hepatitis
  • Cirrhosis
  • MR elastography
  • Primary biliary cirrhosis
  • Primary sclerosing cholangitis

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging
  • Gastroenterology
  • Urology
  • Radiological and Ultrasound Technology

Cite this

Imaging of autoimmune hepatitis and overlap syndromes. / Malik, Neera; Venkatesh, Sudhakar K.

In: Abdominal Radiology, Vol. 42, No. 1, 01.01.2017, p. 19-27.

Research output: Contribution to journalArticle

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