منابع مشابه
Congenital Scaphoid Megalourethra: A Case Report
A congenital megalourethra is an enlargement of the pendulous urethra without evidence of distal obstruction. A 1-month-old boy presented to us with complaint of weak stream, ballooning of the penis before and during voiding and post voiding dribbling, since birth. Physical examination and cystourethroscope confirmed the diagnosis of congenital scaphoid megalourethra. He underwent reduction ure...
متن کاملThe Association of Congenital Urethral Duplication and Double Megalourethra
BACKGROUND Urethral duplication and megalourethra are rare urethral anomalies. However, the concomitance of urethral duplication and double megalourethra has not been reported previously. CASE REPORT A newborn was presented with penile swelling during voiding. Physical examination revealed a retractable foreskin and two external meatus of a double urethra. Retrograde urethrography demonstrate...
متن کاملCongenital hypoplasia of the carpal scaphoid bone.
Three cases of absence of the carpal scaphoid bone have previously been reported in this country (Hodgson 1943, Hanley and Conlon 1957). All three had similar deformities, namely absence or hypoplasia of the carpal scaphoid bone, associated with retardation in the development of the first metacarpal bone, the styloid process of the radius and thenar muscles. While agreeing with these authors th...
متن کاملIndian Pediatrics Megalourethra
Congenital megalourethra is defined as dilatation of anterior urethra due to absence of development or deficiency of erectile tissue of the penis. Since its first description by Nesbitt in 1955, 42 cases have been reported(l,2). The effects of megalourethra as such are not life threatening; they may be deformity of the penis (scaphoid megalourethra) or impotence (fusiform megalourethra). The as...
متن کاملCongenital anterior urethrocutaneous fistula at the penoscrotal junction with proximal penile megalourethra: A case report.
Congenital anterior urethrocutaneous fistula and megalourethra are both rare anomalies. These anomalies are commonly associated with other anorectal or genitourinary anomalies and evaluated with voiding cystourethrography. We examined a 34-month-old boy who presented with a fistula at the penoscrotal junction. A voiding cystourethrogram showed a jet of urine coming through the fistula and proxi...
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ژورنال
عنوان ژورنال: Journal of Pediatric Surgery Case Reports
سال: 2018
ISSN: 2213-5766
DOI: 10.1016/j.epsc.2018.08.005