• Chronic inflammation of the pancreas with fibrosis. It has a relapsing and remitting course and is associated with irreversible impairment of pancreatic function

Causes

  • Similar to acute pancreatitis,
    • Long term alcohol abuse – most common
    • Long term obstruction of the pancreatic duct – gallstones or anatomical abnormalities in the pancreatic duct
    • Tropical pancreatitis – poorly understood, occurs in Africa and Asia
    • Familial pancreatitis – autosomal dominant disorders, the same ones that are associated with acute pancreatitis
    • CF – protein plugging of ducts due to decreased bicarbonate secretion
    • 40% are idiopathic

Pathogenesis

  • Not well understood. Possibilities are;
    • Protein plugging resulting in ductal obstruction – CF and alcohol. Protein plugs may calcify forming calculi
    • Direct acinar cell damage by toxins and oxidative stress
    • Interstitial fibrosis initiated by acute pancreatitis

Morphology

  • Overall the pancreas is hard with focal calcification
  • Chronic inflammation
  • Fibrous scarring with loss of the acinar tissues but relative sparing of the islets of Langerhans until late on in disease
  • Duct strictures with formation of intrapancreatic calculi
  • Other ducts may be dilated and contain protein plugs

Clinical features;

  • Recurrent bouts of severe abdominal pain – attacks may be precipitated by excessive alcohol, eating or drugs
  • Episodes of acute pancreatitis may complicate chronic pancreatitis
  • Later complications are due to loss of exocrine and endocrine function;
    • Malabsorption – diarrhoea, due to decreased lipase and proteinase secretion
    • Steatorrhoea
    • Diabetes mellitus
  • Long term prognosis is poor with only 50% of patients surviving 20-25 years

Investigations

  • Imaging – x-ray, ultrasound, CT, ERCP
  • Functional tests;
  • Secretin/CCK/stimulation test
  • Glucose tolerance test
  • Five day stool collection looking for fat excretion
  • LFT’s
 

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