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PRIMARY BILIARY CIRRHOSIS

PRIMARY BILIARY CIRRHOSIS


PRIMARY BILIARY CIRRHOSIS

  • Also called as primary biliary cholangitis.
  • PBC is the inflammatory autoimmune disease characterised by non suppurative, inflammatory destruction of medium size intrahepatic bile ducts.

    

RISK FACTORS-

  • Familial incidence
  • Elevated cholesterol level with xanthoma and xanthelasma
  • Also associated with-

i) Sjogren’s syndrome (70%)

ii) Thyroid disease (20%)

 

CLINICAL FEATURES-

  • Females are mostly affected (6:1) in 40- 50 years of age
  • It is a cholestatic disorder
  • Persistent pruritis, dark urine, pale stools, steatorrhoea, jaundice
  • Skin pigmentation, lethargy
  • Hepatomegaly
  • Malaise
  • Most common cause of death liver cell failure > variceal bleeding

    

 

INVESTIGATIONS-

  1. Conjugated hyperbilirubinemia
  2. Earliest lab finding- increase serum alkaline phosphatise level
  3. AMA-  positive (95%)
  • M2 form of anti- mitochondrial antibody
  • Most commonly AMA is IgG1 and IgG3 classes
  • ANA positive
  • ANCA positive

    

TREATMENT-

  • Liver transplantation

 

COMPLICATIONS-

  • Portal hypertension
  • Ascites
  • Variceal bleeding

 

Exam Important

CLINICAL FEATURES-
  • Females are mostly affected (6:1) in 40- 50 years of age
  • It is a cholestatic disorder
  • Persistent pruritis, dark urine, pale stools, steatorrhoea, jaundice
  • Skin pigmentation, lethargy
  • Hepatomegaly
  • Malaise
  • Most common cause of death liver cell failure > variceal bleeding

 

 

INVESTIGATIONS-

  1. Conjugated hyperbilirubinemia
  2. Earliest lab finding- increase serum alkaline phosphatise level
  3. AMA-  positive (95%)
  • M2 form of anti- mitochondrial antibody
  • Most commonly AMA is IgG1 and IgG3 classes
  • ANA positive
  • ANCA positive

 

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