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Wegener's Granulomatosis: A Rare Cause of Hydronephrosis

A seventy-one-year-old woman was hospitalized at our institution for a right-sided “renal colic” associated with an infectious background. Alithiasic ureterohydronephrosis was diagnosed by imaging. A urinary diversion was thus performed using a double J endoureteral stent. The etiologic assessment o...

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Autores principales: Lillaz, Julien, Bernardini, Stéphane, Algros, Marie-Paule, Bittard, Hugues, Kleinclauss, François
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090674/
https://www.ncbi.nlm.nih.gov/pubmed/21577265
http://dx.doi.org/10.1155/2011/814794
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author Lillaz, Julien
Bernardini, Stéphane
Algros, Marie-Paule
Bittard, Hugues
Kleinclauss, François
author_facet Lillaz, Julien
Bernardini, Stéphane
Algros, Marie-Paule
Bittard, Hugues
Kleinclauss, François
author_sort Lillaz, Julien
collection PubMed
description A seventy-one-year-old woman was hospitalized at our institution for a right-sided “renal colic” associated with an infectious background. Alithiasic ureterohydronephrosis was diagnosed by imaging. A urinary diversion was thus performed using a double J endoureteral stent. The etiologic assessment of the hydronephrosis showed the presence of a periureteral mass that caused extrinsic ureteral compression. After surgical excision of the ureteral lesion, the Wegener's granulomatosis diagnosis was established. This report is the clinical description of a case of “atypical” Wegener's granulomatosis revealed by the onset of a ureteral disease mimicking a neoplastic process.
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spelling pubmed-30906742011-05-16 Wegener's Granulomatosis: A Rare Cause of Hydronephrosis Lillaz, Julien Bernardini, Stéphane Algros, Marie-Paule Bittard, Hugues Kleinclauss, François Case Rep Med Case Report A seventy-one-year-old woman was hospitalized at our institution for a right-sided “renal colic” associated with an infectious background. Alithiasic ureterohydronephrosis was diagnosed by imaging. A urinary diversion was thus performed using a double J endoureteral stent. The etiologic assessment of the hydronephrosis showed the presence of a periureteral mass that caused extrinsic ureteral compression. After surgical excision of the ureteral lesion, the Wegener's granulomatosis diagnosis was established. This report is the clinical description of a case of “atypical” Wegener's granulomatosis revealed by the onset of a ureteral disease mimicking a neoplastic process. Hindawi Publishing Corporation 2011 2011-03-31 /pmc/articles/PMC3090674/ /pubmed/21577265 http://dx.doi.org/10.1155/2011/814794 Text en Copyright © 2011 Julien Lillaz 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
Lillaz, Julien
Bernardini, Stéphane
Algros, Marie-Paule
Bittard, Hugues
Kleinclauss, François
Wegener's Granulomatosis: A Rare Cause of Hydronephrosis
title Wegener's Granulomatosis: A Rare Cause of Hydronephrosis
title_full Wegener's Granulomatosis: A Rare Cause of Hydronephrosis
title_fullStr Wegener's Granulomatosis: A Rare Cause of Hydronephrosis
title_full_unstemmed Wegener's Granulomatosis: A Rare Cause of Hydronephrosis
title_short Wegener's Granulomatosis: A Rare Cause of Hydronephrosis
title_sort wegener's granulomatosis: a rare cause of hydronephrosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090674/
https://www.ncbi.nlm.nih.gov/pubmed/21577265
http://dx.doi.org/10.1155/2011/814794
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