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Mirizzi syndrome type V complicated with triple fistula: a case report

BACKGROUND: Mirizzi syndrome (MS) is a complicated form of longstanding, symptomatic cholelithiasis. According to Beltran Classification MS Type V has been introduced to describe the cholecystoenteric fistula, with or without gallstone ileus. Mirizzi syndrome Type V with double fistula has been repo...

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Autores principales: Lalountas, Miltiadis, Smyrlis, Nikolaos, Mouratidis, Stylianos Vladimiros, Makedos, Panagiotis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10279597/
https://www.ncbi.nlm.nih.gov/pubmed/37335440
http://dx.doi.org/10.1186/s40792-023-01696-7
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author Lalountas, Miltiadis
Smyrlis, Nikolaos
Mouratidis, Stylianos Vladimiros
Makedos, Panagiotis
author_facet Lalountas, Miltiadis
Smyrlis, Nikolaos
Mouratidis, Stylianos Vladimiros
Makedos, Panagiotis
author_sort Lalountas, Miltiadis
collection PubMed
description BACKGROUND: Mirizzi syndrome (MS) is a complicated form of longstanding, symptomatic cholelithiasis. According to Beltran Classification MS Type V has been introduced to describe the cholecystoenteric fistula, with or without gallstone ileus. Mirizzi syndrome Type V with double fistula has been reported in the past; however, the triple fistula is an even rarer case, first described in the international literature so far. CASE PRESENTATION: A 77-year-old male was admitted to our surgical department with recurrent episodes of abdominal pain, which initially presented in the last 6 months and was accompanied with jaundice. Computed tomography showed findings of cholelithiasis, pneumobilia and choledocholithiasis. We performed an ERCP, which showed two fistulas of the gallbladder with the pyloric antrum and the duodenum, respectively. Surgical treatment was immediately undergone and during laparotomy, we confirmed these findings. We ligated and dissected these communications. In addition, a third fistula between the gallbladder and the common bile duct was identified. An insertion of a Kehr T-tube into the common bile duct was performed via the gallbladder. After 3 months, the Kehr T-tube was removed and in the subsequent 2 years of follow-up the patient was presented without complications. CONCLUSIONS: Mirizzi syndrome complicated with triple fistula, first described in the international literature, to the best of our knowledge, confirms the long natural history of inflammation.
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spelling pubmed-102795972023-06-21 Mirizzi syndrome type V complicated with triple fistula: a case report Lalountas, Miltiadis Smyrlis, Nikolaos Mouratidis, Stylianos Vladimiros Makedos, Panagiotis Surg Case Rep Case Report BACKGROUND: Mirizzi syndrome (MS) is a complicated form of longstanding, symptomatic cholelithiasis. According to Beltran Classification MS Type V has been introduced to describe the cholecystoenteric fistula, with or without gallstone ileus. Mirizzi syndrome Type V with double fistula has been reported in the past; however, the triple fistula is an even rarer case, first described in the international literature so far. CASE PRESENTATION: A 77-year-old male was admitted to our surgical department with recurrent episodes of abdominal pain, which initially presented in the last 6 months and was accompanied with jaundice. Computed tomography showed findings of cholelithiasis, pneumobilia and choledocholithiasis. We performed an ERCP, which showed two fistulas of the gallbladder with the pyloric antrum and the duodenum, respectively. Surgical treatment was immediately undergone and during laparotomy, we confirmed these findings. We ligated and dissected these communications. In addition, a third fistula between the gallbladder and the common bile duct was identified. An insertion of a Kehr T-tube into the common bile duct was performed via the gallbladder. After 3 months, the Kehr T-tube was removed and in the subsequent 2 years of follow-up the patient was presented without complications. CONCLUSIONS: Mirizzi syndrome complicated with triple fistula, first described in the international literature, to the best of our knowledge, confirms the long natural history of inflammation. Springer Berlin Heidelberg 2023-06-19 /pmc/articles/PMC10279597/ /pubmed/37335440 http://dx.doi.org/10.1186/s40792-023-01696-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Case Report
Lalountas, Miltiadis
Smyrlis, Nikolaos
Mouratidis, Stylianos Vladimiros
Makedos, Panagiotis
Mirizzi syndrome type V complicated with triple fistula: a case report
title Mirizzi syndrome type V complicated with triple fistula: a case report
title_full Mirizzi syndrome type V complicated with triple fistula: a case report
title_fullStr Mirizzi syndrome type V complicated with triple fistula: a case report
title_full_unstemmed Mirizzi syndrome type V complicated with triple fistula: a case report
title_short Mirizzi syndrome type V complicated with triple fistula: a case report
title_sort mirizzi syndrome type v complicated with triple fistula: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10279597/
https://www.ncbi.nlm.nih.gov/pubmed/37335440
http://dx.doi.org/10.1186/s40792-023-01696-7
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