Choledochal cyst as an incidental finding during acute cholecystitis: A case report

Key Clinical Message This case demonstrates an atypical presentation of choledochal cysts (CDCs) and elaborates on the diagnostic challenges encountered when presented with CDCs in adulthood, as it principally presents in children. Abstract A choledochal cyst is a rare congenital anomaly characteriz...

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Main Authors: Ryan Isaac Sia Zu Wern, Pravallika Venna, Akash Sarkar, Marwa Abdul‐Haque, Saachi Bhattessa
Format: Article
Language:English
Published: Wiley 2024-02-01
Series:Clinical Case Reports
Subjects:
Online Access:https://doi.org/10.1002/ccr3.8515
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author Ryan Isaac Sia Zu Wern
Pravallika Venna
Akash Sarkar
Marwa Abdul‐Haque
Saachi Bhattessa
author_facet Ryan Isaac Sia Zu Wern
Pravallika Venna
Akash Sarkar
Marwa Abdul‐Haque
Saachi Bhattessa
author_sort Ryan Isaac Sia Zu Wern
collection DOAJ
description Key Clinical Message This case demonstrates an atypical presentation of choledochal cysts (CDCs) and elaborates on the diagnostic challenges encountered when presented with CDCs in adulthood, as it principally presents in children. Abstract A choledochal cyst is a rare congenital anomaly characterized by cystic dilations in the extrahepatic and intrahepatic biliary trees. These cysts are classified according to their location and characteristics. This case study aims to demonstrate how nonspecific clinical features can pose a diagnostic dilemma when presented in adults. Additionally, the case report provides an overview of diagnostic methods and treatment options. In this case, we discuss a 50‐year‐old female who presented with a 2‐ to 3‐day history of severe colicky pain in the right upper quadrant of her abdomen without any other symptoms or abnormal laboratory tests. In addition to ultrasonography evidence of CBD dilation and cholelithiasis, MRCP results confirmed the diagnosis. She underwent surgical intervention involving cyst excision, a Roux‐en‐Y hepatojejunostomy, and a cholecystectomy. The postoperative period was without significant complications. The case presented here illustrates the potential outcomes for individuals who present with choledochal cysts during adulthood. Often, these cases present with vague symptoms or as the underlying cause of a more severe condition. This case contributes to the existing knowledge of choledochal cysts by providing insight into the clinical presentation, diagnostic methods, and treatment options.
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spelling doaj.art-dc87c0cb78a64b6f837c4eea41d898922024-02-29T07:13:20ZengWileyClinical Case Reports2050-09042024-02-01122n/an/a10.1002/ccr3.8515Choledochal cyst as an incidental finding during acute cholecystitis: A case reportRyan Isaac Sia Zu Wern0Pravallika Venna1Akash Sarkar2Marwa Abdul‐Haque3Saachi Bhattessa4GKT School of Medical Education, King's College London Guy's Campus London UKSVS Medical College Mahabubnagar IndiaFaculty of Medicine University of Debrecen Budapest HungaryFaculty of Life Sciences and Education University Of South Wales Cardiff UKVinnytsia National Medical University Vinnytsia Oblast UkraineKey Clinical Message This case demonstrates an atypical presentation of choledochal cysts (CDCs) and elaborates on the diagnostic challenges encountered when presented with CDCs in adulthood, as it principally presents in children. Abstract A choledochal cyst is a rare congenital anomaly characterized by cystic dilations in the extrahepatic and intrahepatic biliary trees. These cysts are classified according to their location and characteristics. This case study aims to demonstrate how nonspecific clinical features can pose a diagnostic dilemma when presented in adults. Additionally, the case report provides an overview of diagnostic methods and treatment options. In this case, we discuss a 50‐year‐old female who presented with a 2‐ to 3‐day history of severe colicky pain in the right upper quadrant of her abdomen without any other symptoms or abnormal laboratory tests. In addition to ultrasonography evidence of CBD dilation and cholelithiasis, MRCP results confirmed the diagnosis. She underwent surgical intervention involving cyst excision, a Roux‐en‐Y hepatojejunostomy, and a cholecystectomy. The postoperative period was without significant complications. The case presented here illustrates the potential outcomes for individuals who present with choledochal cysts during adulthood. Often, these cases present with vague symptoms or as the underlying cause of a more severe condition. This case contributes to the existing knowledge of choledochal cysts by providing insight into the clinical presentation, diagnostic methods, and treatment options.https://doi.org/10.1002/ccr3.8515adultsbiliaryCDCscholedochal cysts
spellingShingle Ryan Isaac Sia Zu Wern
Pravallika Venna
Akash Sarkar
Marwa Abdul‐Haque
Saachi Bhattessa
Choledochal cyst as an incidental finding during acute cholecystitis: A case report
Clinical Case Reports
adults
biliary
CDCs
choledochal cysts
title Choledochal cyst as an incidental finding during acute cholecystitis: A case report
title_full Choledochal cyst as an incidental finding during acute cholecystitis: A case report
title_fullStr Choledochal cyst as an incidental finding during acute cholecystitis: A case report
title_full_unstemmed Choledochal cyst as an incidental finding during acute cholecystitis: A case report
title_short Choledochal cyst as an incidental finding during acute cholecystitis: A case report
title_sort choledochal cyst as an incidental finding during acute cholecystitis a case report
topic adults
biliary
CDCs
choledochal cysts
url https://doi.org/10.1002/ccr3.8515
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AT pravallikavenna choledochalcystasanincidentalfindingduringacutecholecystitisacasereport
AT akashsarkar choledochalcystasanincidentalfindingduringacutecholecystitisacasereport
AT marwaabdulhaque choledochalcystasanincidentalfindingduringacutecholecystitisacasereport
AT saachibhattessa choledochalcystasanincidentalfindingduringacutecholecystitisacasereport