scholarly journals Anterior urethral valves without diverticulum, a rare cause of infravesical obstruction and vesicoureteral reflux in children: Report of two cases and literature review

2017 ◽  
Vol 4 (5) ◽  
pp. 360-363
Author(s):  
Jyoti Bothra ◽  
Charu Tiwari ◽  
Gursev Sandlas ◽  
Hemanshi Shah
2013 ◽  
Vol 2 (2) ◽  
pp. 71-74
Author(s):  
MM Rahman ◽  
PM Rahman ◽  
AR Quddush ◽  
MJ Hasan

The case is presented to discuss clinical signs, diagnostic tools and therapeutics of anterior urethral valves, an obstructive anomaly of the urinary system in males. Signs of urinary tract obstruction were identified on pre-natal ultrasound in a male fetus and the diagnosis of anterior urethral valves was made through post-natal evaluation. As an initial treatment, vesicostomy was performed in the patient. Later, the valve was fulgurated using an endoscopic procedure. During the follow-up period the patient presented normal renal function. Anterior urethral valve is a rare form of urethral anomaly that must be ruled out in boys with pre-natal ultrasound indicating infravesical obstruction. Vesicostomy used as an initial treatment rather than transurethral fulguration may prevent potential complications that can occur due to the small size of the neonatal urethra. DOI: http://dx.doi.org/10.3329/cbmj.v2i2.16703 Community Based Medical Journal 2013 July: Vol.02 No 02: 71-74


2007 ◽  
Vol 3 (5) ◽  
pp. 350-353 ◽  
Author(s):  
Yusuf Kibar ◽  
Hidayet Coban ◽  
H. Cem Irkılata ◽  
Fikret Erdemir ◽  
Bedrettin Seckin ◽  
...  

2008 ◽  
Vol 24 (2) ◽  
pp. 92-95 ◽  
Author(s):  
Haruhiko Sago ◽  
Satoshi Hayashi ◽  
Toshio Chiba ◽  
Katsuhiko Ueoka ◽  
Kentaro Matsuoka ◽  
...  

PEDIATRICS ◽  
1977 ◽  
Vol 60 (5) ◽  
pp. 748-748
Author(s):  
R. Lawrence Kroovand ◽  
Neal Weinberg ◽  
Abbas Emami

Similar congenital anomalies in siblings are common.1-3 Enuresis,4 vesicoureteral reflux,5 and ureteroceles6 have been reported in identical twins, but posterior urethral valves have not been confirmed in proven monozygotic twins. CASE REPORT Twin boys, weighing 2,380 and 2,637 g, were born by repeat cesarean section to an 18-year-old, gravida 2, para 1 woman. The placenta was monochorionic and diamniotic. Immediately after birth, twin A developed grunting respiration and mild substernal retraction; a firm 6 x 5 cm suprapubic mass was palpated. Suprapubic aspiration produced clear urine, and catheterization decreased the size of the mass. A voiding cystourethrogram and an intravenous pyelogram were diagnostic of posterior urethral valves.


Open Medicine ◽  
2013 ◽  
Vol 8 (3) ◽  
pp. 343-345
Author(s):  
Vladimir Kojovic ◽  
Miroslav Djordjevic ◽  
Marta Bizic ◽  
Marko Majstorovic

AbstractCongenital obstruction of the male urethra is usually caused by posterior urethral valves. Anterior urethral valves (AUV) represent a rare anomaly with a wide spectrum of presentation varying from mild voiding difficulties to end-stage renal disease. Prompt diagnosis and appropriate treatment is essential to prevent renal impairment. We report the case of a 13 month-old boy who presented with deterioration of kidney function caused by unrecognized AUV disorder. Temporary cutaneous vesicostomy was necessary to protect the upper urinary tract from further damage and to stabilize renal function. Even though a voiding cystourethrogram (VCUG) demonstrated obstruction of distal urethra, AUV were initially overlooked but finally diagnosed on additional VCUG followed by urethroscopy.


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