HPB Flashcards
causes of pancreatitis
I GET SMASHED
Idiopathic
Gallstones
Ethanol
Trauma (blunt)
Steroids
Mumps
Autoimmune
Scorpion sting - the Trinidad titus trinitatis
Hyperlipidaemia, hypercalcaemia, hyperparathyroidism
ERCP
Drugs - azathioprine
LFTs
raised ALT = specific hepatocyte damage raised AST = hepatocyte, skeletal and cardiac damage AST:ALT >2 = alcoholic liver disease, <1 possibly viral raised ALP = cholestasis or bone raised gamma GT = alcoholic liver disease reduced prothrombin time = liver damage reduced albumin (caused increased cholesterol) = liver damage
causes of jaundice
pre-hepatic (unconjugated hyperbilirubinaemia) –> haemolytic anaemia, malaria, DIC, Gilbert’s/ Criggle-Najjar syndrome
hepatic (mixed hyperbilirubinaemia) –> hepatitis, cirrhosis, syphilis, alcoholic liver disease, HCC, medications
post-hepatic (conjugated hypernilirubinaemia) –> luminal: gallstones, mural: cholangiocarcinoma, strictures, extra-mural: pancreatic cancer, lymphoma
ascending cholangitis
fever, RUQ pain, jaundice (+ hypotension and confusion)
IV Ax and ERCP after 24-48hrs
caused by bacterial infection of biliary tree often ppt by impacted gallstones
biliary colic
postprandial (fatty) RUQ abdo pain with N&V, pain radiates to interscapular region (if diaphragm is irritated)
caused by gallstones in bile duct
DDx are acute cholecystitis but there is no fever or raised inflammatory markers
acute cholecystitis
RUQ pain with fever and raised inflammatory markers
caused by inflammation/ infection secondary to impacted gallstones
+ve Murphy’s sign
acute pancreatitis
very severe epigastric pain that may radiate to the back
O/E tenderness, ileus and low grade fever
assessing severity of pancreatitis
PANCREAS need >3 PaO2 <8kPa Age >55 Neutrophils >15x10^9/L Calcium <2mmol/L Renal function - urea >16mmol/L Enzymes LDH>600iU/L / AST>2000iU/L Albumin <32g/L Sugar >10mmol/L of glucose
gallstone types
cholesterol (yellow, softer)
bile pigment (dark brown/black)
mixed
pancreatic cancer
95% are adenocarcinomas
weight loss, painless jaundice, malaise
only ~ 20% are resectable by Whipple’s
raised CA19-9
USS, CT CAP, PET scan, MRI and laparoscopy to look for micromets on peritoneum
–> IVI, analgesia, CREON. ursodeoxycholic acid, vitamin K, chlorphenamine, thrombophrophlaxis, chemotherapy and nutritional support
what feature of LTFs is present in carcinoma of the head of the pancreas?
the LFTs become deranged
Hepatitis Screen
HBsAg +ve if CURRENTLY infected
anti-HBsAg +ve if RESOLVED infection or IMMUNISED
IgA anti-HBsAg +ve if CHRONICALLY or PREVIOUSLY infected as takes a while to become positive
Wilson’s disease
an autosomal dominant disorder characterised by excessive copper deposition in the tissues
increased copper absorption and reduced hepatic copper excretion = reduced serum copper and increased urinary copper
onset of symptoms between 10-25 y/o in kids more likely to be liver disease (hepatitis, cirrhosis)
whereas adults present with neurological disease (basal ganglia degeneration, speech and behavioural problems)
treatment is penicillamine to chelate the copper
haemochromatosis
autosomal recessive disorder of iron absorption and metabolism resulting in iron accumulation
bronze skin pigmentation
Rx: venesection