• Pancreatic buds (week 4)

    • Develops as 2 separate buds – each an outgrowth of the Endoderm at the junction of the Foregut and Midgut
    • Occurs between 4th and 8th weeks of development
    • Ventral bud:
      • Grows in the Ventral Mesogastrium in common with the outgrowth of the Bile Duct
      • Rotates 270 degrees
    • Dorsal bud:
      • Grows independently from a separate duct into the Dorsal Mesogastrium
      • Rotates 90 degrees
  • Rotation and fusion (week 6)

    • The duodenum undergoes rotation during development, causing the ventral pancreatic bud to rotate and move dorsally.
    • Fusion of the dorsal and ventral pancreatic buds occurs, forming the mature pancreas.
      • Tail, Body, Neck and part of the Head develop from the Dorsal bud
      • Rest of the Head and Uncinate Process develop from the Ventral bud
  • Duct systems of the two buds anastomose

    • Duodenal end of the Dorsal Duct becomes the Accessory Pancreatic Duct
    • Duodenal end of the Ventral Duct joins the remainder of the Dorsal Duct to form the Main Pancreatic Duct
  • Pancreatic acini – develop by growth of cells from terminal parts of the branching ducts

  • Islet cells – identical origin but become separated from their parent ducts and undergo a complete change of secretory function

Abnormalities of Pancreatic Development

Annular Pancreas

  • Partial or complete circumferential encasement of 2nd part of the duodenum by a band of pancreatic tissue
  • Prevalence: 3 per 20,000
  • Aetiology: Migration anomaly – failure of the ventral bud to rotate
  • Clinical: Most remain asymptomatic during lifetime
  • Other possible symptoms:
    • Duodenal constriction – non-bilious vomiting, bloating, feeding intolerance
    • Pancreatitis

Pancreatic divisum

  • Persistence of the dorsal accessory pancreatic duct (of Santorini) with no connection with the main ventral duct (of Wirsung)
  • Failure of fusion of ventral & dorsal ducts in the embryonic pancreas
  • Means main pancreas drains through minor papilla
  • Commonest congenital pancreatic abnormality: 6-10%
  • Found in ≈ 25% of pts with otherwise unexplained pancreatitis
  • Implicated as a cause of acute pancreatitis
  • ? Small / stenotic minor papilla → Intermittent obstruction by proteinaceous plugs
  • Investigations - MRCP / ERCP
  • Management: Recurrent acute pancreatitis may benefit from
  • ERCP & sphincterotomy of minor papilla
  • ± Pancreatic stone extraction / lithotripsy