Cargando…

Congenital intrarenal arteriovenous malformation presenting with gross hematuria after endoscopic intervention: a case report

INTRODUCTION: Although diagnostic ureterorenoscopy is a minimally invasive and effective diagnostic procedure, it has the potential for significant postoperative complications. We report the first case in the literature of intrarenal arteriovenous fistulas causing hemodynamic effective anemia 4 days...

Descripción completa

Detalles Bibliográficos
Autores principales: Seitz, Michael, Waggershauser, Tobias, Khoder, Wael
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2579303/
https://www.ncbi.nlm.nih.gov/pubmed/18847509
http://dx.doi.org/10.1186/1752-1947-2-326
_version_ 1782160568004640768
author Seitz, Michael
Waggershauser, Tobias
Khoder, Wael
author_facet Seitz, Michael
Waggershauser, Tobias
Khoder, Wael
author_sort Seitz, Michael
collection PubMed
description INTRODUCTION: Although diagnostic ureterorenoscopy is a minimally invasive and effective diagnostic procedure, it has the potential for significant postoperative complications. We report the first case in the literature of intrarenal arteriovenous fistulas causing hemodynamic effective anemia 4 days after ureterorenoscopic biopsy. CASE PRESENTATION: A 63-year-old Caucasian woman presented with hemodynamic effective macrohematuria (hemoglobin 70 g/liter) 4 days after ureterorenoscopy and biopsy of the upper pole collecting system due to recurrent microhematuria. Duplex-sonography and computed tomography angiography revealed multiple arteriovenous fistulas and erosions into the calyceal system. Intra-arterial digital subtraction angiography confirmed this condition. After superselective embolization of the arteriovenous fistulas, the patient had no further episodes of bleeding or microhematuria. CONCLUSION: If malignancies, urolithiasis or urinary tract infections are ruled out by common diagnostic procedures as the cause of recurrent minor or gross hematuria, the possibility of arteriovenous fistulas should be included in the differential diagnosis and Duplex-Sonography or the more invasive selective renal arteriography should be performed as this is the most definitive method for diagnosing arteriovenous fistula.
format Text
id pubmed-2579303
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-25793032008-11-05 Congenital intrarenal arteriovenous malformation presenting with gross hematuria after endoscopic intervention: a case report Seitz, Michael Waggershauser, Tobias Khoder, Wael J Med Case Reports Case Report INTRODUCTION: Although diagnostic ureterorenoscopy is a minimally invasive and effective diagnostic procedure, it has the potential for significant postoperative complications. We report the first case in the literature of intrarenal arteriovenous fistulas causing hemodynamic effective anemia 4 days after ureterorenoscopic biopsy. CASE PRESENTATION: A 63-year-old Caucasian woman presented with hemodynamic effective macrohematuria (hemoglobin 70 g/liter) 4 days after ureterorenoscopy and biopsy of the upper pole collecting system due to recurrent microhematuria. Duplex-sonography and computed tomography angiography revealed multiple arteriovenous fistulas and erosions into the calyceal system. Intra-arterial digital subtraction angiography confirmed this condition. After superselective embolization of the arteriovenous fistulas, the patient had no further episodes of bleeding or microhematuria. CONCLUSION: If malignancies, urolithiasis or urinary tract infections are ruled out by common diagnostic procedures as the cause of recurrent minor or gross hematuria, the possibility of arteriovenous fistulas should be included in the differential diagnosis and Duplex-Sonography or the more invasive selective renal arteriography should be performed as this is the most definitive method for diagnosing arteriovenous fistula. BioMed Central 2008-10-12 /pmc/articles/PMC2579303/ /pubmed/18847509 http://dx.doi.org/10.1186/1752-1947-2-326 Text en Copyright © 2008 Seitz et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Seitz, Michael
Waggershauser, Tobias
Khoder, Wael
Congenital intrarenal arteriovenous malformation presenting with gross hematuria after endoscopic intervention: a case report
title Congenital intrarenal arteriovenous malformation presenting with gross hematuria after endoscopic intervention: a case report
title_full Congenital intrarenal arteriovenous malformation presenting with gross hematuria after endoscopic intervention: a case report
title_fullStr Congenital intrarenal arteriovenous malformation presenting with gross hematuria after endoscopic intervention: a case report
title_full_unstemmed Congenital intrarenal arteriovenous malformation presenting with gross hematuria after endoscopic intervention: a case report
title_short Congenital intrarenal arteriovenous malformation presenting with gross hematuria after endoscopic intervention: a case report
title_sort congenital intrarenal arteriovenous malformation presenting with gross hematuria after endoscopic intervention: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2579303/
https://www.ncbi.nlm.nih.gov/pubmed/18847509
http://dx.doi.org/10.1186/1752-1947-2-326
work_keys_str_mv AT seitzmichael congenitalintrarenalarteriovenousmalformationpresentingwithgrosshematuriaafterendoscopicinterventionacasereport
AT waggershausertobias congenitalintrarenalarteriovenousmalformationpresentingwithgrosshematuriaafterendoscopicinterventionacasereport
AT khoderwael congenitalintrarenalarteriovenousmalformationpresentingwithgrosshematuriaafterendoscopicinterventionacasereport