The Gall Bladder and Bile Ducts
The Gall Bladder and Bile Ducts
Surgical Anatomy
• Pear shaped, 7.5 to 12 cm long, normal
capacity – 25-30 ml
• Fundus, body and neck
• Hartmann’s pouch
• Calots triangle
• Moynihans hump
Investigations
• X rays
• Ultrasonography
• Computed tomography
• Magnetic resonance
Cholangiopancreatography
• Endoscopic Retrograde
Cholangiopancreatography
• Percutaneous transhepatic cholangiography
Congenital Abnormalities
• Absent gall bladder
• Phrygian cap
• Floating gall bladder
• Absence of cystic duct
• Low insertion of cystic duct
Extra hepatic Biliary Atresia
• Atresia is present in 1/12000 live births
• Males = females
• Progressive destruction of EHBR around the
time of birth
• Intra hepatic changes can also occur –
resulting in biliary cirrhosis and portal
hypertension
• Clinical features
– Jaundice at birth
– Pale coloured stools
– Osteomalacia
– Pruritis
– Clubbing, Skin Xanthomas
• D/D
– Alpha 1 anti trypsin deficiency
– Cholestasis associated with IV feeding
– Choledochal cyst
– Inspissated bile syndrome
• Treatment
– Roux en Y Hepatico Jejunostomy
– Kasai Procedure (Porto enterostomy)
– Liver transplantation
• Complications
– Bacterial cholangitis
– Hepatic fibrosis
– Portal Hypertension
Caroli’s Disease
• Multiple irregular saccular dilatations of the intrahepatic
ducts, separated by normal or stenotic ducts
• Associated with congenital hepatic fibrosis
• C/F – abdominal pain, cholangitis or end stage liver
disease
• Management –
– IV antibiotics
– Stenting
– Hepatic resection
– Liver Transplantation
Choledochal cyst