ReviewDigestive diseases and sciences2025
Diagnosis and Treatment of Choledochal Cysts: A Comprehensive Review with a Focus on Choledochocele.
Review in Digestive diseases and sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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Who cites it
9 citing papers in PubMed.
- The SHAP Has Sailed: Explainable Machine Learning Meets Endoscopic Ultrasonography in the Diagnosis of Non-pancreatic Periampullary Lesions.Digestive diseases and sciences · 2026Article
- A Rare Case of Dual Cystic Ducts.Cureus · 2026Article
- Laparoscopic management of cystic duct cyst (Type VI): case report.Journal of surgical case reports · 2026Article
- Preoperative nutritional risk and adverse perioperative outcomes in children with congenital choledochal cysts: a retrospective cohort study.Frontiers in pediatrics · 2026Article
- Treatment of giant choledochal cysts with combined surgery and percutaneous transhepatic cholangial drainage: A case report.World journal of gastrointestinal surgery · 2025Article
- A comparative study of childhood versus adult-onset biliary complications following pediatric choledochal cyst surgery.Pediatric surgery international · 2025Article
- Type IVa bile duct dilatation in an adult female treated with living donor liver transplantation.Hepatobiliary surgery and nutrition · 2025Article
- Global research trends in surgical management of choledochal cysts: a bibliometric analysis from 2000 to 2024.Frontiers in medicine · 2025Article
- Learning curve comparison of robot-assisted and laparoscopic hepaticojejunostomy: a focus on critical suturing.Frontiers in pediatrics · 2025Article
Corrections and comments
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Authors and funding
17 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Choledochal cysts (CCs) are cystic dilations of intrahepatic and/or extrahepatic bile ducts. Around 80% of CCs are diagnosed within the first decade of life. These complex clinical entities are extremely rare, especially in the Western population. CCs are frequently classified according to the Todani classification. CCs may be asymptomatic or present as acute pancreatitis and/or cholangitis, biliary obstruction, or malignancy. Therefore, the diagnosis relies primarily on abdominal imaging modalities, mainly magnetic resonance cholangiopancreatography. Management is tailored based on the cyst morphology and the patient's clinical characteristics, with surveillance, surgery, and interventional endoscopy being the most frequent management options. While the surgical approach is the most frequently employed, type III CCs (also known as choledochocele) are frequently managed endoscopically, and novel endoscopic, minimally invasive treatment options are rapidly emerging.
Indexed as
Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.