Manipal Journal of Medical Sciences
Abstract
Choledochal cysts are rare congenital abnormalities of the biliary tract (1), with an incidence of 1:1000 births in the Asian population, with a female predominance. They usually appear within the first decade of life, presenting with symptoms like abdominal pain, jaundice, and a palpable abdominal mass. Todani et al. (2) classified them into five types. Common diagnostic techniques include ultrasound, CT, MRCP and ERCP. This case report presents a 14-year-old female with a giant type 1 choledochal cyst, successfully managed with cholecystectomy and Roux-en-Y jejunostomy.
Recommended Citation
Saxena, Isha; J, Naresh Kumar; Raghupal, Pareekshith; Rai, Santosh; and Joshi, Jayateertha
(2025)
"Beyond the Ordinary: A Case Report on a Giant Choledochal Cyst,"
Manipal Journal of Medical Sciences: Vol. 10:
Iss.
1, Article 8.
DOI: https://doi.org/10.55889/2582-5984.1175
Available at:
https://impressions.manipal.edu/mjms/vol10/iss1/8
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