VURD Syndrome Managed by Pyelostomy

We report a case of VURD syndrome in a three day old neonate who was diagnosed with hydronephrosis on a prenatal ultrasound. Severe tortuosity and dilation of the upper urinary tracts in the presence of progression of hydronephrosis or a persistently elevated creatinine may favor a proximal urinary...

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Main Authors: Charles J. Rosser, Sam Auringer, R. L. Kroovand
Format: Article
Language:English
Published: Wiley 2004-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/tsw.2004.80
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author Charles J. Rosser
Sam Auringer
R. L. Kroovand
author_facet Charles J. Rosser
Sam Auringer
R. L. Kroovand
author_sort Charles J. Rosser
collection DOAJ
description We report a case of VURD syndrome in a three day old neonate who was diagnosed with hydronephrosis on a prenatal ultrasound. Severe tortuosity and dilation of the upper urinary tracts in the presence of progression of hydronephrosis or a persistently elevated creatinine may favor a proximal urinary diversion rather than primary valve ablation or cutaneous vesicostomy. Because of a persistently elevated serum creatinine, a nonfunctioning kidney with grade 4/5 vesicoureteral reflux and worsening contralateral hydronephrosis despite lower tract drainage, a left cutaneous pyelostomy was performed, contralateral to the kidney involved with VURD. Postoperatively the serum creatinine stabilized at 1.0 mg/dl and decreased to 0.3 mg/dl at one month of age.
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series The Scientific World Journal
spelling doaj-art-3a76aa714e7f4b3a949a6d57e7a5a1472025-02-03T07:24:31ZengWileyThe Scientific World Journal1537-744X2004-01-01438238610.1100/tsw.2004.80VURD Syndrome Managed by PyelostomyCharles J. Rosser0Sam Auringer1R. L. Kroovand2Department of Urology, Bowman Gray School of Medicine Wake Forest University, Winston-Salem, North Carolina, USADepartment of Urology, Bowman Gray School of Medicine Wake Forest University, Winston-Salem, North Carolina, USADepartment of Urology, Bowman Gray School of Medicine Wake Forest University, Winston-Salem, North Carolina, USAWe report a case of VURD syndrome in a three day old neonate who was diagnosed with hydronephrosis on a prenatal ultrasound. Severe tortuosity and dilation of the upper urinary tracts in the presence of progression of hydronephrosis or a persistently elevated creatinine may favor a proximal urinary diversion rather than primary valve ablation or cutaneous vesicostomy. Because of a persistently elevated serum creatinine, a nonfunctioning kidney with grade 4/5 vesicoureteral reflux and worsening contralateral hydronephrosis despite lower tract drainage, a left cutaneous pyelostomy was performed, contralateral to the kidney involved with VURD. Postoperatively the serum creatinine stabilized at 1.0 mg/dl and decreased to 0.3 mg/dl at one month of age.http://dx.doi.org/10.1100/tsw.2004.80
spellingShingle Charles J. Rosser
Sam Auringer
R. L. Kroovand
VURD Syndrome Managed by Pyelostomy
The Scientific World Journal
title VURD Syndrome Managed by Pyelostomy
title_full VURD Syndrome Managed by Pyelostomy
title_fullStr VURD Syndrome Managed by Pyelostomy
title_full_unstemmed VURD Syndrome Managed by Pyelostomy
title_short VURD Syndrome Managed by Pyelostomy
title_sort vurd syndrome managed by pyelostomy
url http://dx.doi.org/10.1100/tsw.2004.80
work_keys_str_mv AT charlesjrosser vurdsyndromemanagedbypyelostomy
AT samauringer vurdsyndromemanagedbypyelostomy
AT rlkroovand vurdsyndromemanagedbypyelostomy