Endoscopic cystostomy and biliary sphincterotomy for choledochoceles: A pediatric case series

Michelle Saad1,2, Maisam Abu-El-Haija1,2, Tom K Lin1,2

  • 1Division of Gastroenterology, Hepatology and Nutrition Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA.

JPGN Reports
|November 29, 2024
PubMed

Insights

Endoscopic management of choledochoceles (type III choledochal cysts) in children offers a successful treatment option. This minimally invasive approach led to sustained symptom resolution and radiographic improvement in pediatric patients.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Endoscopic Procedures

Background:

  • Choledochoceles, a type of choledochal cyst, present varied management challenges in pediatric patients.
  • Symptoms often include abdominal pain and pancreatitis, necessitating effective treatment strategies.

Purpose of the Study:

  • To evaluate the efficacy of endoscopic management for pediatric choledochoceles.
  • To assess the long-term outcomes of cystostomy and biliary sphincterotomy in children with choledochoceles.

Main Methods:

  • Retrospective review of three pediatric patients (ages 12-13) with symptomatic choledochoceles.
  • Endoscopic cystostomy and biliary sphincterotomy performed for choledochal cyst treatment.
  • Pre- and post-procedure imaging (MRI) and tumor marker assessment.

Main Results:

  • Successful endoscopic treatment of choledochoceles in all three pediatric patients.
  • Sustained clinical improvement and radiographic resolution at 2-year follow-up.
  • Normal tumor markers post-procedure, indicating no malignancy.

Conclusions:

  • Endoscopic management with cystostomy and biliary sphincterotomy is a viable therapeutic option for pediatric choledochoceles.
  • This approach can achieve sustained symptom resolution and radiographic healing.
  • Malignancy risk in choledochoceles is rare, supporting less invasive treatment modalities.

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