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Related Concept Videos

Gastritis III: Clinical Manifestations and Management01:23

Gastritis III: Clinical Manifestations and Management

The clinical manifestations of gastritis can vary depending on the cause and type of gastritis, but some common symptoms may include the following.
Clinical manifestations of acute gastritis
The patient with acute gastritis may have a rapid onset of symptoms, such as epigastric pain or discomfort, dyspepsia, anorexia, hiccups, or nausea and vomiting, which can last from a few hours to a few days. Erosive or hemorrhagic gastritis may cause bleeding, which may manifest as blood in vomit or as...
Viral Hepatitis I: Introduction01:28

Viral Hepatitis I: Introduction

Viral hepatitis is an inflammatory condition of the liver caused by infection with hepatotropic viruses, most commonly hepatitis A, B, C, D, and E. Despite variations in structure and transmission, all viruses mentioned infect hepatocytes and provoke immune responses that can hinder liver function. Additionally, some non-hepatotropic viruses can also lead to hepatic inflammation.Hepatitis A VirusHepatitis A virus (HAV) is transmitted through the fecal–oral route, typically by ingestion of food...
Hepatitis01:25

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Hepatitis is an inflammatory condition of the liver most commonly caused by hepatotropic viruses (A–E), though non-infectious causes such as alcohol and drugs also exist.Hepatitis AHepatitis A virus (HAV) is a non-enveloped RNA virus of the Picornaviridae family. It is primarily transmitted via the fecal-oral route, typically through ingestion of contaminated food or water. After ingestion, HAV enters the bloodstream through the oropharynx or intestinal epithelium and reaches the liver. The...
Acute Pancreatitis II: Clinical Manifestations and Management01:30

Acute Pancreatitis II: Clinical Manifestations and Management

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Autoimmune Disorders01:29

Autoimmune Disorders

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Gastritis-II: Pathophysiology01:17

Gastritis-II: Pathophysiology

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Related Experiment Video

Updated: Jun 3, 2026

The CYP2D6 Animal Model: How to Induce Autoimmune Hepatitis in Mice
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The CYP2D6 Animal Model: How to Induce Autoimmune Hepatitis in Mice

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[Autoimmune hepatitis: two case reports with different clinical courses - case 3/2011].

L Minkley1, P Adam, R Klein

  • 1Medizinische Klinik, Abteilung für Gastroenterologie, Hepatologie und Infektiologie, Universitätsklinikum Tübingen, Tübingen. ena.minkley@med.unituebingen.de

Deutsche Medizinische Wochenschrift (1946)
|March 5, 2011
PubMed
Summary

Autoimmune hepatitis, a rare liver disease, presents with elevated liver enzymes and responds well to prednisolone treatment. Early diagnosis and immunosuppressive therapy are crucial for improving patient prognosis and preventing advanced disease requiring liver transplantation.

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Last Updated: Jun 3, 2026

The CYP2D6 Animal Model: How to Induce Autoimmune Hepatitis in Mice
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Induction of Drug-Induced, Autoimmune Hepatitis in BALB/c Mice for the Study of Its Pathogenic Mechanisms
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Preparation of Mouse Pituitary Immunogen for the Induction of Experimental Autoimmune Hypophysitis
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Preparation of Mouse Pituitary Immunogen for the Induction of Experimental Autoimmune Hypophysitis

Published on: December 17, 2010

Area of Science:

  • Hepatology
  • Immunology
  • Internal Medicine

Background:

  • Autoimmune hepatitis (AIH) is a rare, chronic liver disease characterized by autoimmune-mediated liver inflammation.
  • Diagnosis can be challenging due to varied presentations and exclusion of other liver diseases.

Observation:

  • Two female patients presented with jaundice, elevated liver enzymes, and hypergammaglobulinaemia.
  • Both patients tested negative for viral hepatitis and showed high titers of antinuclear antibodies (ANA) and smooth muscle antibodies (SMA).
  • Liver biopsies confirmed autoimmune hepatitis in both cases.

Findings:

  • Both patients responded well to high-dose prednisolone therapy, with significant improvement in clinical and laboratory parameters.
  • Case 1 showed rapid recovery, while Case 2 experienced a slower recovery with complications requiring further management.
  • Advanced disease in Case 2 may necessitate a future liver transplantation.

Implications:

  • Prompt investigation of elevated liver enzymes is essential for early AIH diagnosis.
  • Immunosuppressive therapy, particularly with prednisolone, is effective in managing AIH.
  • Timely diagnosis and treatment significantly improve patient outcomes and prognosis, potentially avoiding the need for liver transplantation.