Cargando…

Is It Really SUMP Syndrome? A Case Report

Sump syndrome is a rare, long-term complication with a prevalence ranging from 0% to 9.6% in patients with a history of side-to-side choledochoduodenostomy. Choledochoduodenostomy was originally performed to achieve drainage of the common bile duct in high-risk patients with low morbidity, which was...

Descripción completa

Detalles Bibliográficos
Autores principales: Suliman, Mohamed S, Singh, Monider M, Zaheer, Kamran, Malik, Saad Ullah, Abu-Hashyeh, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827695/
https://www.ncbi.nlm.nih.gov/pubmed/31754572
http://dx.doi.org/10.7759/cureus.5837
_version_ 1783465340941893632
author Suliman, Mohamed S
Singh, Monider M
Zaheer, Kamran
Malik, Saad Ullah
Abu-Hashyeh, Ahmad
author_facet Suliman, Mohamed S
Singh, Monider M
Zaheer, Kamran
Malik, Saad Ullah
Abu-Hashyeh, Ahmad
author_sort Suliman, Mohamed S
collection PubMed
description Sump syndrome is a rare, long-term complication with a prevalence ranging from 0% to 9.6% in patients with a history of side-to-side choledochoduodenostomy. Choledochoduodenostomy was originally performed to achieve drainage of the common bile duct in high-risk patients with low morbidity, which was commonly done in the pre-endoscopic retrograde cholangiopancreatography era. “Sump” comes from the segment of the common bile duct between the anastomosis and the ampulla of Vater, which acts as a stagnant reservoir for debris, stones, and static bile. This predisposes patients to changes in the biliary tree with signs and symptoms in relation to that area. If left untreated, cholangitis, pancreatitis, hepatic abscesses, and secondary biliary cirrhosis can develop. Here, we have a case of a 77-year-old male with a history significant for choledochoduodenostomy, who presented with the clinical signs and symptoms of pancreatitis, choledocholithiasis, and urinary tract infection. Computed tomography (CT) scan findings revealed choledocholithiasis and an enlarged common bile duct with smaller adjacent calculi along with pneumobilia consistent with sump syndrome. The patient’s clinical status improved without invasive measures being taken, i.e. endoscopic retrograde cholangiopancreatography. He was subsequently discharged home after improving clinically and no invasive measures were pursued.
format Online
Article
Text
id pubmed-6827695
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Cureus
record_format MEDLINE/PubMed
spelling pubmed-68276952019-11-21 Is It Really SUMP Syndrome? A Case Report Suliman, Mohamed S Singh, Monider M Zaheer, Kamran Malik, Saad Ullah Abu-Hashyeh, Ahmad Cureus General Surgery Sump syndrome is a rare, long-term complication with a prevalence ranging from 0% to 9.6% in patients with a history of side-to-side choledochoduodenostomy. Choledochoduodenostomy was originally performed to achieve drainage of the common bile duct in high-risk patients with low morbidity, which was commonly done in the pre-endoscopic retrograde cholangiopancreatography era. “Sump” comes from the segment of the common bile duct between the anastomosis and the ampulla of Vater, which acts as a stagnant reservoir for debris, stones, and static bile. This predisposes patients to changes in the biliary tree with signs and symptoms in relation to that area. If left untreated, cholangitis, pancreatitis, hepatic abscesses, and secondary biliary cirrhosis can develop. Here, we have a case of a 77-year-old male with a history significant for choledochoduodenostomy, who presented with the clinical signs and symptoms of pancreatitis, choledocholithiasis, and urinary tract infection. Computed tomography (CT) scan findings revealed choledocholithiasis and an enlarged common bile duct with smaller adjacent calculi along with pneumobilia consistent with sump syndrome. The patient’s clinical status improved without invasive measures being taken, i.e. endoscopic retrograde cholangiopancreatography. He was subsequently discharged home after improving clinically and no invasive measures were pursued. Cureus 2019-10-04 /pmc/articles/PMC6827695/ /pubmed/31754572 http://dx.doi.org/10.7759/cureus.5837 Text en Copyright © 2019, Suliman et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle General Surgery
Suliman, Mohamed S
Singh, Monider M
Zaheer, Kamran
Malik, Saad Ullah
Abu-Hashyeh, Ahmad
Is It Really SUMP Syndrome? A Case Report
title Is It Really SUMP Syndrome? A Case Report
title_full Is It Really SUMP Syndrome? A Case Report
title_fullStr Is It Really SUMP Syndrome? A Case Report
title_full_unstemmed Is It Really SUMP Syndrome? A Case Report
title_short Is It Really SUMP Syndrome? A Case Report
title_sort is it really sump syndrome? a case report
topic General Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827695/
https://www.ncbi.nlm.nih.gov/pubmed/31754572
http://dx.doi.org/10.7759/cureus.5837
work_keys_str_mv AT sulimanmohameds isitreallysumpsyndromeacasereport
AT singhmoniderm isitreallysumpsyndromeacasereport
AT zaheerkamran isitreallysumpsyndromeacasereport
AT maliksaadullah isitreallysumpsyndromeacasereport
AT abuhashyehahmad isitreallysumpsyndromeacasereport