HPB Flashcards
Define jaundice
Yellow discolouration of sclera and skin
Due to hyperbilirubinaemia
Pathophysiology of jaundice
High levels of bilirubin in blood
Normal breakdown product from catabolism of haem
Normally conjugated within liver - water-soluble
Excreted via bile into GI tract
Types of jaundice
Pre-hepatic - excessive red cell breakdown - unconjugated bilirubin Hepatocellular - dysfunction of hepatic cells - mixed bilirubin Post-hepatic - obstruction of biliary drainage - conjugated bilirubin
Causes of pre-hepatic jaundice
Haemolytic anaemia
Gilbert’s syndrome
Criggler-Najjar syndrome
Causes of hepatocellular jaundice
Alcoholic liver disease Viral hepatitis Iatrogenic - medication Hereditary haemochromatosis Autoimmune hepatitis PBC or PSC Hepatocellular carcinoma
Causes of post-hepatic jaundice
Intraluminal - gallstones Mural - cholangiocarcinoma - strictures - drug-induced cholestasis Extra-mural - pancreatic cancer - abdominal masses
Investigations for jaundice
LFTs
- AST and ALT raised in hepatocellular injury
- ALP raised in biliary obstruction
- Gamma-GT more specific for biliary obstruction
Coagulation studies
FBC - anaemia, raised MCV and thrombocytopenia seen in liver disease
Bilirubin
Albumin - marker of liver synthesising function
USS abdomen
MRCP
Liver biopsy
Management of jaundice
ERCP - gallstone removal
Symptomatic treatment for itching
Identify and manage complications
Monitor for coagulopathy
Define a simple liver cysts
Fluid-filled epithelial-lined sacs
Most commonly in the right lobe
Thought to be due to congenitally malformed bile duct cells
Clinical features of simple liver cysts
Normally asymptomatic - often detect incidentally
Abdominal pain, nausea and early satiety
Investigations for simple liver cysts
LFTs normal - may have raised GGT
USS imaging
- anechoic
- well-defined
- thin-walled
- oval/spherical lesions with no septations
- strong posterior wall acoustic enchancement
Management of simple cysts
< 4cm - no intervention
> 4cm - USS follow-up at 3,6 and 12 months
USS guided aspiration
Laparoscopic de-roofing
Define polycystic liver disease
Presence of > 20 cysts within the liver parechyma
Caused by
- Autosomal dominant polycystic kidney disease
- Autosomal dominant polycystic liver disease
Clinical features of polycystic liver disease
Majority asymptomatic
Abdominal pain as cysts grow in size
Investigations for polycystic liver disease
Normal LFTs
USS imaging - demonstrates multiple cysts
Management of polycystic liver disease
Asymptomatic left alone
Somatostatin analogues
USS guided aspiration
Laparacopic de-roofing of cysts
Define a cystic neoplasm
Cystadenoma - non-invasive mucinous cystic neoplasms
Premalignant lesions
Clinical features of cystic neoplasms
Asymptomatic
Abdominal pain
Anorexia
Investigations for cystic neoplasms
LFTs are normal
CT imaging with contrast
Management for cystic neoplasm
Liver lobe resection
Avoid aspiration or biopsy - potential peritoneal seeding
Define a liver absces
Polymicrobial bacterial infection spread from biliary or gastrointestinal tract
Common causes of liver absces
Cholecystitis Cholangitis Diverticulitits Appendicitis Septicaemia
Common causative organisms of liver abscesses
E.coli
K.pneumoniae
S.constellatus
Clinical features of liver abscesses
Fever Rigors Abdo pain RUQ tenderness +/- hepatomegaly Shock if ruptures