3. What is
Cirrhosis
• Defined histopathologically
• Development of fibrosis leading
to architectural distortion with
the formation of regenerative
nodules.
• This results in:
Decrease in cell mass, and
thus function
An alteration of blood flow
4. Causes of Cirrhosis
90%
40%
40-45%
40-45%
Alcoholic Cirrhosis
(Western Statistics)
Cirrhosis due to
Chronic hepatitis B or
C infection
Cirrhosis due to
Autoimmune hepatitis
and Non Alcoholic
Steatohepatitis
Others:
Biliary Cirrhosis
Cardiac Cirrhosis
Cryptogenic Cirrhosis
Cirrhosis due to
metabolic disorders
8. Investigations
CBC:
Anemia.
Thrombocytopenia
LFTs:
Serum total bilirubin elevated with advanced disease
ALT, AST are elevated, A/G ratio is usually 2:1 ratio in severe heapatocellular damage
Elevated GGT and ALP (in cholestasis)
Albumin levels are decreased
Prothrombin times are prolonged
S/E:
Serum sodium levels are decreased if patient has ascites largely due to ingestion of excess free water.
Viral studies:
Auto immune markers:
Anti ANA, anti ASMA antibodies (AIH)
Anti mitochondrial antibodies (PBC)
P-ANCA (PSC)
Imaging Studies
Endoscopy
Iron studies and copper studies
Liver Biopsy: (most specific)
Micronodular cirrhosis: Alcoholic cirrhosis
Macronodular cirrhosis
Mixed pattern: Hepatitis C
Non invasive markers
9. Staging the
Disease
• Compensated cirrhosis
• Decompensated cirrhosis
•Portal hypertension leading to
ascities and bleeding from varices
•Portosystemic encephalopathy
Anemia due to blood loss, nutritional deficiencies, or hypersplenism related to portal hypertension, or as a direct suppressive effect of alcohol on the bone marrow
Hypersplenism
Iaging: usg, cholangiography, mrcp, ercp,
Alpha macroglobin, hepatoglobin