• 2% of all malignancies
  • Generally in males >60
  • Risk factors – smoking, alcohol, diabetes, chronic pancreatitis
  • 95% have mutations in the KRAS2 gene
  • Mostly ductal adenocarcinomas – 60% in head, 25% in body, 15% in tail
  • A few arise in the Ampulla of vater or pancreatic islet cells and have better prognosis

Symptoms and signs

  • Tumours in the head of the pancreas present with painless jaundice
  • 75% of tumours in the body and the tail present with epigastric pain which radiates to the back and is relieved by sitting forward
  • Either may cause anorexia, diabetes, acute pancreatitis
  • Rarer features;
    • Thrombophebitis migrans – arm vein becomes swollen and red and then a leg vein
    • Raised calcium
    • Marantic endocarditis
    • Portal hypertension (splenic vein thrombosis)
    • Nephrosis (renal vein thrombosis)

Other signs

  • Jaundice plus palpable gallbladder
  • Epigastric mass
  • Hepatomegaly
  • Splenomegaly
  • Lymphadenopathy
  • Ascites

Test

  • Bloods – cholestatic picture plus raised Ca19-9
  • US/CT

Treatment

  • Less than 10% are suitable for radical surgery
  • Do a pancreatoduodenectomy (Whipple’s) if fit, tumour <3cm and no mets
  • Post op chemo may delay disease progession
  • Consider palliation of jaundice
  • Pain relief – may require large doses of opiates – can infiltrate the coeliac axis with alcohol at the time of surgery or later percutaenously

Prognosis

  • Poor – <6mth mean, 5 year survival <2%
 

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