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Chronic abdominal pain leads to discovery of congenital anomaly

A 43-year-old female with no history of a cholecystectomy presented with chronic right sided abdominal pain that became worse after fatty food intake. This led to an extensive workup for gallbladder disease for the patient’s source of her pain. She had an initial ultrasound, which showed a collapsed...

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Detalles Bibliográficos
Autores principales: Uddin, Fahad K, Sampson, Lorenzo K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420560/
https://www.ncbi.nlm.nih.gov/pubmed/36042893
http://dx.doi.org/10.1093/jscr/rjac381
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author Uddin, Fahad K
Sampson, Lorenzo K
author_facet Uddin, Fahad K
Sampson, Lorenzo K
author_sort Uddin, Fahad K
collection PubMed
description A 43-year-old female with no history of a cholecystectomy presented with chronic right sided abdominal pain that became worse after fatty food intake. This led to an extensive workup for gallbladder disease for the patient’s source of her pain. She had an initial ultrasound, which showed a collapsed gallbladder around gallstones, which signified chronic cholecystitis. This was confirmed with a hepatobiliary iminodiacetic acid scan with Choletec and morphine as there was no visualization of the gallbladder. Due to the patient’s persistent abdominal pain with associated symptoms and radiographic evidence of cholecystitis, she was taken to the operating theater for a laparoscopic cholecystectomy and the absence of a gallbladder was discovered. The goal of this clinical case report is to highlight this rare anomaly and how it presents in a clinical setting.
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spelling pubmed-94205602022-08-29 Chronic abdominal pain leads to discovery of congenital anomaly Uddin, Fahad K Sampson, Lorenzo K J Surg Case Rep Case Report A 43-year-old female with no history of a cholecystectomy presented with chronic right sided abdominal pain that became worse after fatty food intake. This led to an extensive workup for gallbladder disease for the patient’s source of her pain. She had an initial ultrasound, which showed a collapsed gallbladder around gallstones, which signified chronic cholecystitis. This was confirmed with a hepatobiliary iminodiacetic acid scan with Choletec and morphine as there was no visualization of the gallbladder. Due to the patient’s persistent abdominal pain with associated symptoms and radiographic evidence of cholecystitis, she was taken to the operating theater for a laparoscopic cholecystectomy and the absence of a gallbladder was discovered. The goal of this clinical case report is to highlight this rare anomaly and how it presents in a clinical setting. Oxford University Press 2022-08-27 /pmc/articles/PMC9420560/ /pubmed/36042893 http://dx.doi.org/10.1093/jscr/rjac381 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2022. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Uddin, Fahad K
Sampson, Lorenzo K
Chronic abdominal pain leads to discovery of congenital anomaly
title Chronic abdominal pain leads to discovery of congenital anomaly
title_full Chronic abdominal pain leads to discovery of congenital anomaly
title_fullStr Chronic abdominal pain leads to discovery of congenital anomaly
title_full_unstemmed Chronic abdominal pain leads to discovery of congenital anomaly
title_short Chronic abdominal pain leads to discovery of congenital anomaly
title_sort chronic abdominal pain leads to discovery of congenital anomaly
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420560/
https://www.ncbi.nlm.nih.gov/pubmed/36042893
http://dx.doi.org/10.1093/jscr/rjac381
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