Pathologies

1.1 Acute infectious hepatitis is mainly caused by the specific hepatitis viruses, namely A, B, C and E

1.2 Toxic Liver Disease (Drug Induced Liver Injury)

1.3 Acute Liver Failure (ALF)

2.1 Chronic hepatitis

2.2 Cholestatic liver diseases

2.3 Congenital Storage Diseases (metabolic disorders)

2.4 Steatotic liver diseases

3.1 Portal vein thrombosis (without cirrhosis)

3.2 Budd-Chiari syndrome

3.3 Sinusoidal obstructive syndrome (SOS)

3.4 Rendu-Osler-Weber disease (hereditary hemorrhagic telangiectasia)

3.5 Idiopathic non-cirrhotic portal hypertension

4.1 Polycystic liver disease (CLD)

5.1 Prognostic scores

5.2 Coagulation disorders

5.3 Acute chronic liver failure (ACLF) and decompensated cirrhosis

5.4 Portal hypertension

5.5 Esophageal Varices Bleeding

5.6 Other Causes of Gastrointestinal Bleeding in Cirrhosis

5.7 Ascites

5.8 Complications of Ascites

5.9 Hepatic Encephalopathy (HE)

5.10 Rare Complications Portal Hypertension

6.1 Main indications

7.1 Intrahepatic cholestasis of pregnancy (IHCP)

7.2 HELLP syndrome

7.3 Acute Fatty Liver of pregnancy (AFLP)

9.1 Pyogenic liver abscess

9.2 Amoebic liver abscess

9.3 Echinococcus cyst

9.4 Isolated biliary cysts

9.5 Hemangioma

9.6 Adenoma

9.7 Focal nodular hyperplasia (FNH)