Literature DB >> 33613964

Surgical management of a massive choledochal cyst.

Atta Nawabi1, Javaneh Jabbari1, Perwaiz Nawabi2.   

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. Published by Oxford University Press and JSCR Publishing Ltd.
© The Author(s) 2021.

Entities:  

Year:  2021        PMID: 33613964      PMCID: PMC7884067          DOI: 10.1093/jscr/rjab006

Source DB:  PubMed          Journal:  J Surg Case Rep        ISSN: 2042-8812


  1 in total

1.  Challenges of Surgical Treatment of Atypical Giant Choledochal Cyst with the Absence of Gallbladder in Adult Patient.

Authors:  Ismar Rasic; Nermin Mahmutovic; Samir Custovic; Nedim Hasic; Ali Gavrankapetanovic; Edin Beciragic; Sanela Brzika
Journal:  Case Rep Surg       Date:  2022-04-20
  1 in total

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