Literature DB >> 21565560

Vesicoureteral reflux in children with urachal anomalies.

Janelle A Fox1, Shawn M McGee, Jonathan C Routh, Candace F Granberg, Richard A Ashley, Joel C Hutcheson, David R Vandersteen, Yuri E Reinberg, Stephen A Kramer.   

Abstract

OBJECTIVE: We report the largest known series of vesicoureteral reflux (VUR) in children with urachal anomalies (UA).
METHODS: Two institutions' records were reviewed for children with UA (1951‒2007).
RESULTS: Of 30 girls and 36 boys with UA (34 urachal cysts, 14 patent urachus, 10 urachal diverticula, 7 urachal sinuses, and 1 unknown), 57 (86%) underwent surgical resection or drainage. A voiding cystourethrogram was obtained in 22 (33%). VUR was demonstrated in 14 of the 22 children (64%), and rates were similar among the various types of UA. The median age with versus without VUR was not different (1.3 vs 1.7 years, P=0.97). Of 24 refluxing renal units, classification was grade≤3 in 71%, 4‒5 in 12%, and unspecified in 17%. Four children (26%) underwent ureteroneocystostomy and 10 observed patients resolved spontaneously.
CONCLUSION: To our knowledge, this is the first series of VUR associated with UA. The increased incidence of VUR (64%) in this small subset of patients warrants prospective studies to determine if there is a positive correlation with UA. We believe thorough genitourinary and family histories are important when evaluating children with UA to help detect clinically significant VUR.
Copyright © 2011. Published by Elsevier Ltd.

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Year:  2011        PMID: 21565560     DOI: 10.1016/j.jpurol.2011.04.001

Source DB:  PubMed          Journal:  J Pediatr Urol        ISSN: 1477-5131            Impact factor:   1.830


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2.  Improved laparoscopic treatment of symptomatic urachal anomalies.

Authors:  Maciej Patrzyk; Lutz Wilhelm; Kaja Ludwig; Claus Dieter Heidecke; Wolfram von Bernstorff
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3.  Posterior urethral valve with unilateral vesicoureteral reflux and patent urachus: A rare combination of urinary tract anomaliess.

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  3 in total

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