Gall Bladder Duplication with Choledochal Cyst: A Rare Entity

A 4-year-old male child presented with complaints of abdominal pain and vomiting along with yellowish discoloration of the eyes. Investigations were suggestive of acute pancreatitis and double gall bladder (GB) with dilated common bile duct (CBD) with intraluminal calculi and Type II choledochal cys...

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Autores principales: Sharma, Rahul Deo, Sushma, Achugatla, Singh, Surendra, Tewari, Shruti, Redkar, Rajeev
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455702/
https://www.ncbi.nlm.nih.gov/pubmed/37635883
http://dx.doi.org/10.4103/jiaps.jiaps_20_23
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author Sharma, Rahul Deo
Sushma, Achugatla
Singh, Surendra
Tewari, Shruti
Redkar, Rajeev
author_facet Sharma, Rahul Deo
Sushma, Achugatla
Singh, Surendra
Tewari, Shruti
Redkar, Rajeev
author_sort Sharma, Rahul Deo
collection PubMed
description A 4-year-old male child presented with complaints of abdominal pain and vomiting along with yellowish discoloration of the eyes. Investigations were suggestive of acute pancreatitis and double gall bladder (GB) with dilated common bile duct (CBD) with intraluminal calculi and Type II choledochal cyst. He underwent surgical resection of double GB with dilated CBD with hepatico-docho-jejunostomy. On follow-up, the patient was asymptomatic. Our case highlights the importance of preoperative diagnosis to deal with increased operative difficulty and complications.
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spelling pubmed-104557022023-08-26 Gall Bladder Duplication with Choledochal Cyst: A Rare Entity Sharma, Rahul Deo Sushma, Achugatla Singh, Surendra Tewari, Shruti Redkar, Rajeev J Indian Assoc Pediatr Surg Case Report A 4-year-old male child presented with complaints of abdominal pain and vomiting along with yellowish discoloration of the eyes. Investigations were suggestive of acute pancreatitis and double gall bladder (GB) with dilated common bile duct (CBD) with intraluminal calculi and Type II choledochal cyst. He underwent surgical resection of double GB with dilated CBD with hepatico-docho-jejunostomy. On follow-up, the patient was asymptomatic. Our case highlights the importance of preoperative diagnosis to deal with increased operative difficulty and complications. Wolters Kluwer - Medknow 2023 2023-07-11 /pmc/articles/PMC10455702/ /pubmed/37635883 http://dx.doi.org/10.4103/jiaps.jiaps_20_23 Text en Copyright: © 2023 Journal of Indian Association of Pediatric Surgeons https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Sharma, Rahul Deo
Sushma, Achugatla
Singh, Surendra
Tewari, Shruti
Redkar, Rajeev
Gall Bladder Duplication with Choledochal Cyst: A Rare Entity
title Gall Bladder Duplication with Choledochal Cyst: A Rare Entity
title_full Gall Bladder Duplication with Choledochal Cyst: A Rare Entity
title_fullStr Gall Bladder Duplication with Choledochal Cyst: A Rare Entity
title_full_unstemmed Gall Bladder Duplication with Choledochal Cyst: A Rare Entity
title_short Gall Bladder Duplication with Choledochal Cyst: A Rare Entity
title_sort gall bladder duplication with choledochal cyst: a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455702/
https://www.ncbi.nlm.nih.gov/pubmed/37635883
http://dx.doi.org/10.4103/jiaps.jiaps_20_23
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