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Spontaneous biliary peritonitis with common bile duct stones: report of a case

Spontaneous biliary peritonitis is rare in adults. We herein report a case of spontaneous biliary peritonitis. An 84-year-old man was admitted to our hospital for abdominal pain for 5 days. He developed fever, jaundice, and abdominal rigidity. Computed tomography (CT) revealed massive ascites in the...

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Autores principales: Hamura, Ryoga, Haruki, Koichiro, Tsutsumi, Jun, Takayama, Sumio, Shiba, Hiroaki, Yanaga, Katsuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039139/
https://www.ncbi.nlm.nih.gov/pubmed/27679466
http://dx.doi.org/10.1186/s40792-016-0234-6
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author Hamura, Ryoga
Haruki, Koichiro
Tsutsumi, Jun
Takayama, Sumio
Shiba, Hiroaki
Yanaga, Katsuhiko
author_facet Hamura, Ryoga
Haruki, Koichiro
Tsutsumi, Jun
Takayama, Sumio
Shiba, Hiroaki
Yanaga, Katsuhiko
author_sort Hamura, Ryoga
collection PubMed
description Spontaneous biliary peritonitis is rare in adults. We herein report a case of spontaneous biliary peritonitis. An 84-year-old man was admitted to our hospital for abdominal pain for 5 days. He developed fever, jaundice, and abdominal rigidity. Computed tomography (CT) revealed massive ascites in the omental bursa and around the liver. The ascites obtained by diagnostic paracentesis was dark yellow-green in color, which implied bile leakage. With a diagnosis of bile peritonitis, the patient underwent emergency exploratory laparotomy. There was massive biliary ascites in the abdominal cavity, especially in the omental bursa. Because exploration failed to demonstrate the perforation site in the gallbladder and biliary duct, we performed abdominal lavage alone. Postoperative endoscopic retrograde cholangiopancreatography showed stones in the common bile duct, and there was no evidence of biliary leakage. Endoscopic retrograde biliary drainage was performed using a plastic stent to reduce the pressure of the common bile duct. After the operation, the patient showed satisfactory recovery and started oral intake on postoperative day 8. However, the patient developed heart failure due to renal dysfunction with nephrotic syndrome at 1 month after the operation. With a diagnosis of rapidly progressive glomerulonephritis due to immune complex, the patient received steroid treatment for nephritis, diuretics, and carperitide for heart failure. Although heart failure and renal dysfunction improved by these treatment, the patients developed toxic epidermal necrolysis which was refractory to intensive treatments including steroid pulse and immunoglobulin, and the patient died 76 days after the operation.
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spelling pubmed-50391392016-10-11 Spontaneous biliary peritonitis with common bile duct stones: report of a case Hamura, Ryoga Haruki, Koichiro Tsutsumi, Jun Takayama, Sumio Shiba, Hiroaki Yanaga, Katsuhiko Surg Case Rep Case Report Spontaneous biliary peritonitis is rare in adults. We herein report a case of spontaneous biliary peritonitis. An 84-year-old man was admitted to our hospital for abdominal pain for 5 days. He developed fever, jaundice, and abdominal rigidity. Computed tomography (CT) revealed massive ascites in the omental bursa and around the liver. The ascites obtained by diagnostic paracentesis was dark yellow-green in color, which implied bile leakage. With a diagnosis of bile peritonitis, the patient underwent emergency exploratory laparotomy. There was massive biliary ascites in the abdominal cavity, especially in the omental bursa. Because exploration failed to demonstrate the perforation site in the gallbladder and biliary duct, we performed abdominal lavage alone. Postoperative endoscopic retrograde cholangiopancreatography showed stones in the common bile duct, and there was no evidence of biliary leakage. Endoscopic retrograde biliary drainage was performed using a plastic stent to reduce the pressure of the common bile duct. After the operation, the patient showed satisfactory recovery and started oral intake on postoperative day 8. However, the patient developed heart failure due to renal dysfunction with nephrotic syndrome at 1 month after the operation. With a diagnosis of rapidly progressive glomerulonephritis due to immune complex, the patient received steroid treatment for nephritis, diuretics, and carperitide for heart failure. Although heart failure and renal dysfunction improved by these treatment, the patients developed toxic epidermal necrolysis which was refractory to intensive treatments including steroid pulse and immunoglobulin, and the patient died 76 days after the operation. Springer Berlin Heidelberg 2016-09-27 /pmc/articles/PMC5039139/ /pubmed/27679466 http://dx.doi.org/10.1186/s40792-016-0234-6 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Report
Hamura, Ryoga
Haruki, Koichiro
Tsutsumi, Jun
Takayama, Sumio
Shiba, Hiroaki
Yanaga, Katsuhiko
Spontaneous biliary peritonitis with common bile duct stones: report of a case
title Spontaneous biliary peritonitis with common bile duct stones: report of a case
title_full Spontaneous biliary peritonitis with common bile duct stones: report of a case
title_fullStr Spontaneous biliary peritonitis with common bile duct stones: report of a case
title_full_unstemmed Spontaneous biliary peritonitis with common bile duct stones: report of a case
title_short Spontaneous biliary peritonitis with common bile duct stones: report of a case
title_sort spontaneous biliary peritonitis with common bile duct stones: report of a case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039139/
https://www.ncbi.nlm.nih.gov/pubmed/27679466
http://dx.doi.org/10.1186/s40792-016-0234-6
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