Authors :
Dr. J. G. Vagadiya; Dr. Pooja Patel
Volume/Issue :
Volume 11 - 2026, Issue 1 - January
Google Scholar :
https://tinyurl.com/2sdhxsc3
Scribd :
https://tinyurl.com/4aj3v8vz
DOI :
https://doi.org/10.38124/ijisrt/26jan706
Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.
Abstract :
Choledochal cysts are rare developmental anomalies involving intrahepatic and extrahepatic biliary ducts whose complete excision is recommended to prevent chronic inflammatory and malignant changes. During embryonic development, the pancreatic duct and common bile duct join abnormally outside the duodenal wall, forming a long common channel. This allows pancreatic enzyme reflux into the bile duct. Enzymes cause chronic inflammation and weakening of the bile duct wall. The weakened duct progressively dilates → forming a choledochal cyst.
Keywords :
Choledochal Cyst, Type 1 C, Female Child, Hepaticojejunostomy.
References :
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Choledochal cysts are rare developmental anomalies involving intrahepatic and extrahepatic biliary ducts whose complete excision is recommended to prevent chronic inflammatory and malignant changes. During embryonic development, the pancreatic duct and common bile duct join abnormally outside the duodenal wall, forming a long common channel. This allows pancreatic enzyme reflux into the bile duct. Enzymes cause chronic inflammation and weakening of the bile duct wall. The weakened duct progressively dilates → forming a choledochal cyst.
Keywords :
Choledochal Cyst, Type 1 C, Female Child, Hepaticojejunostomy.