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Gallbladder Agenesis with Refractory Choledocholithiasis

Congenital agenesis of the gallbladder is a rare anomaly which is usually asymptomatic and found incidentally. In some cases, however, patients are symptomatic. Common symptoms include right upper quadrant abdominal pain, nausea, and vomiting. Jaundice is present in some symptomatic cases and is due...

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Detalles Bibliográficos
Autores principales: Tjaden, Jamie, Patel, Kevin, Aadam, Aziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491557/
https://www.ncbi.nlm.nih.gov/pubmed/26185691
http://dx.doi.org/10.1155/2015/747931
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author Tjaden, Jamie
Patel, Kevin
Aadam, Aziz
author_facet Tjaden, Jamie
Patel, Kevin
Aadam, Aziz
author_sort Tjaden, Jamie
collection PubMed
description Congenital agenesis of the gallbladder is a rare anomaly which is usually asymptomatic and found incidentally. In some cases, however, patients are symptomatic. Common symptoms include right upper quadrant abdominal pain, nausea, and vomiting. Jaundice is present in some symptomatic cases and is due to associated choledocholithiasis (Fiaschetti et al. 2009). In this case, a 63-year-old female presents with jaundice and episodic right upper quadrant abdominal pain with nausea and vomiting. Bilirubin and alkaline phosphatase were found to be markedly elevated. Upper endoscopic ultrasound (EUS) revealed choledocholithiasis, and the patient required multiple endoscopic retrograde cholangiopancreatography (ERCP) sessions before successful extraction of all stones. Subsequent surgical exploration revealed congenital agenesis of the gallbladder. Although this is a rare finding, patients with agenesis of the gallbladder are at increased risk of developing de novo choledocholithiasis which may be challenging to extract.
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spelling pubmed-44915572015-07-16 Gallbladder Agenesis with Refractory Choledocholithiasis Tjaden, Jamie Patel, Kevin Aadam, Aziz Case Rep Gastrointest Med Case Report Congenital agenesis of the gallbladder is a rare anomaly which is usually asymptomatic and found incidentally. In some cases, however, patients are symptomatic. Common symptoms include right upper quadrant abdominal pain, nausea, and vomiting. Jaundice is present in some symptomatic cases and is due to associated choledocholithiasis (Fiaschetti et al. 2009). In this case, a 63-year-old female presents with jaundice and episodic right upper quadrant abdominal pain with nausea and vomiting. Bilirubin and alkaline phosphatase were found to be markedly elevated. Upper endoscopic ultrasound (EUS) revealed choledocholithiasis, and the patient required multiple endoscopic retrograde cholangiopancreatography (ERCP) sessions before successful extraction of all stones. Subsequent surgical exploration revealed congenital agenesis of the gallbladder. Although this is a rare finding, patients with agenesis of the gallbladder are at increased risk of developing de novo choledocholithiasis which may be challenging to extract. Hindawi Publishing Corporation 2015 2015-06-22 /pmc/articles/PMC4491557/ /pubmed/26185691 http://dx.doi.org/10.1155/2015/747931 Text en Copyright © 2015 Jamie Tjaden et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Tjaden, Jamie
Patel, Kevin
Aadam, Aziz
Gallbladder Agenesis with Refractory Choledocholithiasis
title Gallbladder Agenesis with Refractory Choledocholithiasis
title_full Gallbladder Agenesis with Refractory Choledocholithiasis
title_fullStr Gallbladder Agenesis with Refractory Choledocholithiasis
title_full_unstemmed Gallbladder Agenesis with Refractory Choledocholithiasis
title_short Gallbladder Agenesis with Refractory Choledocholithiasis
title_sort gallbladder agenesis with refractory choledocholithiasis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491557/
https://www.ncbi.nlm.nih.gov/pubmed/26185691
http://dx.doi.org/10.1155/2015/747931
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