Published online Jun 27, 2025. doi: 10.4240/wjgs.v17.i6.107351
Revised: April 18, 2025
Accepted: May 9, 2025
Published online: June 27, 2025
Processing time: 62 Days and 2.9 Hours
Choledochal cyst is a rare biliary tract disorder with five subtypes categorized based on the anatomical location of cystic dilatation. Type IV (which affects the intrahepatic and extrahepatic ducts) is the most common subtype in adults. Its clinical manifestations are diverse and the disease can potentially become malignant. Currently, the mainstay treatment is surgical excision which is used as a definitive treatment to prevent complications and avoid carcinogenesis. However, the surgical operation for giant choledochal cysts is technically chal
Here, we present a case of a giant choledochal cyst in an 18-year-old female. The diagnosis of patient was confirmed through magnetic resonance cholangiopancreatography. The patient developed acute cholangitis, and was treated with percutaneous transhepatic cholangial drainage to alleviate symptoms. The final treatment approach was cyst excision followed by Roux-en-Y hepaticojejunostomy, which successfully achieved excellent postoperative recovery.
Ultrasonography and magnetic resonance cholangiopancreatography can effe
Core Tip: Giant choledochal cysts are exceedingly rare in clinical practice. Here, we report a case of an 18-year-old female with a massive choledochal cyst complicated with acute cholangitis. Magnetic resonance cholangiopancreatography was performed, which facilitated the attainment of a confirmatory diagnosis, while percutaneous transhepatic cholangial drainage combined with definitive surgical intervention resulted in successful clinical outcomes. The present case highlights the critical significance of advanced imaging modalities in the diagnosis of giant choledochal cysts and highlights the efficacy of staged management (drainage followed by excision) for giant choledochal cysts. And the benefits of artificial intelligence systems for surgery are also discussed. These results provide crucial insights that can be used to optimize future diagnostic and therapeutic strategies for this rare biliary disorder.