Case Report: A rare case of choledochal cyst [version 1; peer review: 2 approved]

Autor: Amit Singh, Sulav Deo, Sushil Rayamajhi, Wasiq Bin Tariq, Azwar Anjum, Neela Sunuwar, Anu Radha Twayana
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: F1000Research, Vol 11 (2022)
Druh dokumentu: article
ISSN: 2046-1402
DOI: 10.12688/f1000research.123930.1
Popis: Background: Choledochal cysts are dilated portions of the biliary tract that account for 1% of all benign biliary diseases. It is prevalent among Asian and female populations and the incidence is 1:100,000–150,000. Among the different types, only 15–35% of all choledochal cysts are type IV cysts, with type I being the most common representing 50–80%. Clinical presentation and therapy of biliary cysts (BC) differ depending on the type. Case: We present a case of a 2-year-old male who presented with non-specific symptoms of multiple episodes of vomiting. Laboratory investigations revealed raised alkaline phosphatase and gamma-glutamyl transpeptidase. His symptoms of acute pancreatitis were resolved with conventional therapy. Ultrasonography of the abdomen showed intra and extra-hepatic cystic biliary tree dilatation suggestive of choledochal cyst Type IV A. Conclusions: Choledochal cysts present with clinical features varying with age and anatomical variants and can pose challenges in management that can be addressed by surgery to avoid further complications.
Databáze: Directory of Open Access Journals