Postnatal rupture of an antenatally diagnosed choledochal cyst: first case report

Mohammad M F Siddiqui1, David Grier, Eleri Cusick

  • 1Department of Paediatric Surgery, Bristol Children's Hospital, Bristol, UK.

Insights

Prompt pediatric surgical referral is crucial for antenatal diagnosed choledochal cysts. Even asymptomatic cysts can rupture if surgical intervention is delayed, necessitating emergency surgery.

Area of Science:

  • Pediatric Surgery
  • Congenital Abnormalities
  • Gastrointestinal Surgery

Background:

  • Choledochal cysts are rare congenital dilations of the bile ducts.
  • Antenatal diagnosis allows for early management planning.
  • Management typically involves surgical excision.

Observation:

  • A 7-month-old infant with an asymptomatic antenatally diagnosed choledochal cyst presented for elective surgery.
  • The cyst ruptured prior to the scheduled surgery, requiring emergency laparotomy.
  • The patient recovered uneventfully after the urgent surgical intervention.

Findings:

  • Delayed surgical intervention for choledochal cysts, even when asymptomatic, carries a risk of rupture.
  • Rupture can occur unexpectedly after initial diagnosis and planning for elective surgery.
  • Prompt surgical referral is essential for optimal patient outcomes.

Implications:

  • Antenatal diagnosis of choledochal cysts necessitates timely surgical consultation and intervention.
  • Proactive surgical management can prevent complications such as cyst rupture.
  • This case highlights the importance of avoiding delays in pediatric surgical referrals for congenital anomalies.
Abstract