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Bilobed gallbladder discovered during laparoscopic cholecystectomy: a tale of two lobes and one duct

Bilobed gallbladder (BG) is a rare congenital anomaly with just 24 cases documented in medical literature in the past 127 years. There are only three documented cases of BG’s managed with laparoscopic cholecystectomy, and in all three cases the bilobed anomaly was discovered preoperatively. We prese...

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Autores principales: Plewman, Devon, Kudrna, Rachel, Rojas, Oskar, Ford, Jennifer, Smith-Singares, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718324/
https://www.ncbi.nlm.nih.gov/pubmed/34992770
http://dx.doi.org/10.1093/jscr/rjab579
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author Plewman, Devon
Kudrna, Rachel
Rojas, Oskar
Ford, Jennifer
Smith-Singares, Eduardo
author_facet Plewman, Devon
Kudrna, Rachel
Rojas, Oskar
Ford, Jennifer
Smith-Singares, Eduardo
author_sort Plewman, Devon
collection PubMed
description Bilobed gallbladder (BG) is a rare congenital anomaly with just 24 cases documented in medical literature in the past 127 years. There are only three documented cases of BG’s managed with laparoscopic cholecystectomy, and in all three cases the bilobed anomaly was discovered preoperatively. We present a case of symptomatic cholelithiasis in a BG that was discovered intraoperatively. Both the surgical techniques used to ensure complete and safe removal of all gallbladder components and the elements associated with the preoperative diagnosis of these rare anomalies are discussed.
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spelling pubmed-87183242022-01-05 Bilobed gallbladder discovered during laparoscopic cholecystectomy: a tale of two lobes and one duct Plewman, Devon Kudrna, Rachel Rojas, Oskar Ford, Jennifer Smith-Singares, Eduardo J Surg Case Rep Case Report Bilobed gallbladder (BG) is a rare congenital anomaly with just 24 cases documented in medical literature in the past 127 years. There are only three documented cases of BG’s managed with laparoscopic cholecystectomy, and in all three cases the bilobed anomaly was discovered preoperatively. We present a case of symptomatic cholelithiasis in a BG that was discovered intraoperatively. Both the surgical techniques used to ensure complete and safe removal of all gallbladder components and the elements associated with the preoperative diagnosis of these rare anomalies are discussed. Oxford University Press 2021-12-30 /pmc/articles/PMC8718324/ /pubmed/34992770 http://dx.doi.org/10.1093/jscr/rjab579 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2021. 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
Plewman, Devon
Kudrna, Rachel
Rojas, Oskar
Ford, Jennifer
Smith-Singares, Eduardo
Bilobed gallbladder discovered during laparoscopic cholecystectomy: a tale of two lobes and one duct
title Bilobed gallbladder discovered during laparoscopic cholecystectomy: a tale of two lobes and one duct
title_full Bilobed gallbladder discovered during laparoscopic cholecystectomy: a tale of two lobes and one duct
title_fullStr Bilobed gallbladder discovered during laparoscopic cholecystectomy: a tale of two lobes and one duct
title_full_unstemmed Bilobed gallbladder discovered during laparoscopic cholecystectomy: a tale of two lobes and one duct
title_short Bilobed gallbladder discovered during laparoscopic cholecystectomy: a tale of two lobes and one duct
title_sort bilobed gallbladder discovered during laparoscopic cholecystectomy: a tale of two lobes and one duct
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718324/
https://www.ncbi.nlm.nih.gov/pubmed/34992770
http://dx.doi.org/10.1093/jscr/rjab579
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