Rupture in Polycystic Kidney Disease Presented as Generalized Peritonitis with Severe Sepsis: A Rare Case Report

Recurrent upper urinary tract (renal) infections have been reported to be frequent in patients with autosomal dominant polycystic kidney disease and often difficult to treat. Female preference and enteric organism predominance suggest that these renal infections are acquired to retrograde from the l...

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Autores principales: Zahir, Muhammed, Al Muttairi, Hassan, Upadhyay, Surjya Prasad, Mallick, Piyush N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600282/
https://www.ncbi.nlm.nih.gov/pubmed/23533936
http://dx.doi.org/10.1155/2013/927676
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author Zahir, Muhammed
Al Muttairi, Hassan
Upadhyay, Surjya Prasad
Mallick, Piyush N.
author_facet Zahir, Muhammed
Al Muttairi, Hassan
Upadhyay, Surjya Prasad
Mallick, Piyush N.
author_sort Zahir, Muhammed
collection PubMed
description Recurrent upper urinary tract (renal) infections have been reported to be frequent in patients with autosomal dominant polycystic kidney disease and often difficult to treat. Female preference and enteric organism predominance suggest that these renal infections are acquired to retrograde from the lower urinary tract. We encountered a rare case of bilateral polycystic kidneys with spontaneous intraperitoneal rupture of multiple infected renal cysts causing generalized peritonitis leading to severe sepsis with multiorgan failure. The patient is successfully managed with nephrectomy followed by prolonged supportive care in intensive care unit.
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spelling pubmed-36002822013-03-26 Rupture in Polycystic Kidney Disease Presented as Generalized Peritonitis with Severe Sepsis: A Rare Case Report Zahir, Muhammed Al Muttairi, Hassan Upadhyay, Surjya Prasad Mallick, Piyush N. Case Rep Urol Case Report Recurrent upper urinary tract (renal) infections have been reported to be frequent in patients with autosomal dominant polycystic kidney disease and often difficult to treat. Female preference and enteric organism predominance suggest that these renal infections are acquired to retrograde from the lower urinary tract. We encountered a rare case of bilateral polycystic kidneys with spontaneous intraperitoneal rupture of multiple infected renal cysts causing generalized peritonitis leading to severe sepsis with multiorgan failure. The patient is successfully managed with nephrectomy followed by prolonged supportive care in intensive care unit. Hindawi Publishing Corporation 2013 2013-02-28 /pmc/articles/PMC3600282/ /pubmed/23533936 http://dx.doi.org/10.1155/2013/927676 Text en Copyright © 2013 Muhammed Zahir et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Zahir, Muhammed
Al Muttairi, Hassan
Upadhyay, Surjya Prasad
Mallick, Piyush N.
Rupture in Polycystic Kidney Disease Presented as Generalized Peritonitis with Severe Sepsis: A Rare Case Report
title Rupture in Polycystic Kidney Disease Presented as Generalized Peritonitis with Severe Sepsis: A Rare Case Report
title_full Rupture in Polycystic Kidney Disease Presented as Generalized Peritonitis with Severe Sepsis: A Rare Case Report
title_fullStr Rupture in Polycystic Kidney Disease Presented as Generalized Peritonitis with Severe Sepsis: A Rare Case Report
title_full_unstemmed Rupture in Polycystic Kidney Disease Presented as Generalized Peritonitis with Severe Sepsis: A Rare Case Report
title_short Rupture in Polycystic Kidney Disease Presented as Generalized Peritonitis with Severe Sepsis: A Rare Case Report
title_sort rupture in polycystic kidney disease presented as generalized peritonitis with severe sepsis: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600282/
https://www.ncbi.nlm.nih.gov/pubmed/23533936
http://dx.doi.org/10.1155/2013/927676
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