Document Type
Article
Publication Title
Journal of Surgical Case Reports
Abstract
Choledochal cysts (CC) are congenital bile duct anomalies, typically present in children. The size of CC vary, but they rarely exceed 9 cm. Surgical resection is the mainstay of treatment. This case report presents 18-year-old female with jaundice and abdominal pain. On imaging she was found to have a type I CC versus a type IVa CC. She was taken to the operating room where she was found to have a 20 cm type I CC. The patient experienced complete recovery after total resection of the extrahepatic cyst with reconstruction with a Roux-en-Y hepaticojejunostomy. Preoperative diagnosis of the type of CCs can be challenging. Proper imaging preoperatively can aid in diagnosis of these cysts, but delineation of anatomy and type may not always be possible. If treated in a timely manner, it can help prevent both long- and short-term complications.
DOI
10.1093/jscr/rjab006
Publication Date
2-14-2021
Keywords
abdominal pain, choledochal cyst, cysts, jaundice, preoperative care, reconstructive surgical procedures, surgical procedures, diagnostic imaging, excision, bile duct abnormalities
ISSN
2042-8812
Recommended Citation
Nawabi A, Jabbari J, Nawabi P. Surgical Management of a Massive Choledochal Cyst. Journal of Surgical Case Reports. 2021; 2021(2). doi: 10.1093/jscr/rjab006.