Multiple urethral anomalies: Anterior urethral diverticulum, posterior urethral valves, and distal hypospadias

2013 ◽  
Vol 48 (1) ◽  
pp. e5-e8 ◽  
Author(s):  
Ravibindu Ranawaka ◽  
Alan P. Dickson
Author(s):  
Kim Hutton ◽  
Ashok Daya Ram

Most disorders of the urethra in children are congenital in origin and affect boys more commonly than girls. They include; posterior urethral valves (PUV), anterior urethral valves, anterior urethral diverticulum, syringocele, urethral atresia, megalourethra, urethral web, urethral polyp, and urethral duplication. Urethral strictures may be congenital or acquired. Most cases of PUV are now diagnosed prenatally. Postnatal management comprises bladder drainage, correction of any metabolic disturbance, prevention of infection (UTI), and endoscopic valve ablation. Careful follow up is required with the aim of preventing urosepsis and preserving renal function. Persisting bladder dysfunction (‘valve’ bladder) can threaten renal function and should be managed aggressively. Chronic renal failure ultimately affects a third of boys with PUV, of whom 10–20% require renal transplantation during the course of childhood. PUV may also present clinically with recurrent UTI, urinary incontinence, or unexplained lower urinary tract symptoms.


2016 ◽  
Vol 49 (02) ◽  
pp. 265-267 ◽  
Author(s):  
Annavarupu Gopalkrishna ◽  
Somendra Mohan Sharma ◽  
B. Ananda

ABSTRACTCongenital anomalies of the urogenital tract are the most common anomalies found in the foetus, neonates and infants, but anterior urethral valves and diverticula are rare. Here, we present a case with congenital anterior urethral diverticulum associated with patent ductus arteriosus and polydactyly.


2000 ◽  
Vol 4 (2) ◽  
pp. 118-122 ◽  
Author(s):  
P Lopez Pereira ◽  
E. Jaureguizar ◽  
M. J Martinez Urrutia ◽  
C Meseguer ◽  
M Navarro

2003 ◽  
Vol 33 (11) ◽  
pp. 794-796
Author(s):  
Gaurav Saigal ◽  
George Abdenour ◽  
E. Michael Azouz ◽  
Sudha D Lolayekar

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