Aplasia of the dorsal pancreas and choledochal cyst

Noboru Oyachi1, Youkatsu Ohhama, Hiroshi Take

  • 1Department of Surgery, Kanagawa Children's Medical Center, 2-138-4 Mutsukawa, Minami-ku, 232-8555, Yokohama, Kanagawa, Japan. noyachi@hotmail.com

Insights

This study reports a rare case of a choledochal cyst and dorsal pancreatic aplasia in a child, leading to chronic pancreatitis. Surgical intervention successfully managed the obstructive jaundice and cyst.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Congenital Anomalies

Background:

  • Choledochal cysts are rare congenital biliary tract malformations.
  • Dorsal pancreatic aplasia is a rare congenital anomaly of the pancreas.
  • Chronic pancreatitis can result from various underlying conditions.

Observation:

  • A 9-year-old boy presented with obstructive jaundice, a symptom of biliary tract issues.
  • The patient was diagnosed with a choledochal cyst and aplasia of the dorsal pancreas.
  • Chronic pancreatitis was identified as a complication in this case.

Findings:

  • The case highlights the uncommon co-occurrence of choledochal cyst and dorsal pancreatic aplasia.
  • This specific combination was complicated by the development of chronic pancreatitis.
  • The patient underwent successful management including percutaneous transhepatic gallbladder drainage (PTGBD) and surgical excision.

Implications:

  • This case expands the understanding of rare congenital anomalies and their pancreatic complications.
  • It underscores the importance of considering complex congenital associations in pediatric obstructive jaundice.
  • The successful surgical outcome provides a potential management pathway for similar rare presentations.

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