Choledochal Cyst in Children, presentation and outcome - 10 years' experience from a tertiary care center in Pakistan

Muhammad Arslan Farooq1, Sabeen Abid Khan2, Munir Iqbal Malik3

  • 1Dr. Muhammad Arslan Farooq, MBBS, FCPS (Pediatrics). Senior Registrar, Pediatrics, Shifa Tameer-e-Millat University (Shifa College of Medicine)/ Shifa International Hospital, Islamabad, Pakistan.

Insights

Pediatric choledochal cysts present differently in infants versus older children. Surgical excision is the best treatment, and early intervention prevents complications.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Medical Diagnostics

Background:

  • Choledochal cysts are congenital bile duct anomalies with variable clinical presentations.
  • Understanding age-specific features is crucial for timely diagnosis and management.

Purpose of the Study:

  • To compare clinical features, laboratory findings, and surgical outcomes in infant and pediatric patients with choledochal cysts.
  • To analyze the impact of age on presentation and complications.

Main Methods:

  • Retrospective review of hospital records for pediatric patients diagnosed with choledochal cysts between 2011 and 2021.
  • Patients were categorized into infant (<1 year) and pediatric (1-16 years) groups for comparative analysis.

Main Results:

  • 34 children were included: 9 infants and 25 older pediatric patients. Type-I choledochal cysts were most common (73.5%).
  • Infants commonly presented with jaundice (77.7%), while older children experienced abdominal pain (88%), vomiting (72%), and pancreatitis (32%).
  • Overall post-surgical complication rate was 11.7%.

Conclusions:

  • Choledochal cyst presentation varies significantly with patient age.
  • Complete surgical excision is the preferred treatment, and prompt surgical intervention is key to preventing complications.
Abstract

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