Case Report: A rare case of choledochal cyst.

Autor: Tariq WB; Emergency Medicine, Kulhudhuffushi Regional Hospital, Kulhudhuffushi, 02110, Maldives., Twayana AR; Internal Medicine, Bhaktapur Hospital, Bhaktapur, 44800, Nepal., Sunuwar N; Emergency Medicine, Kulhudhuffushi Regional Hospital, Kulhudhuffushi, 02110, Maldives., Anjum A; Emergency Medicine, Kulhudhuffushi Regional Hospital, Kulhudhuffushi, 02110, Maldives., Deo S; Internal Medicine, Suraksha Hospital, Biratnagar, 56613, Nepal., Rayamajhi S; Internal Medicine, Swacon International Hospital, Kathmandu, 44600, Nepal., Singh A; Health Emergency Intervention, Consultant Surgeon, World Health Organization, Nepal, Kathmandu, 44600, Nepal.
Jazyk: angličtina
Zdroj: F1000Research [F1000Res] 2022 Aug 10; Vol. 11, pp. 919. Date of Electronic Publication: 2022 Aug 10 (Print Publication: 2022).
DOI: 10.12688/f1000research.123930.1
Abstrakt: 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.
Competing Interests: No competing interests were disclosed.
(Copyright: © 2022 Tariq WB et al.)
Databáze: MEDLINE