Complete Urethral Duplication in Children: A Case Report
نویسندگان
چکیده
INTRODUCTION Urethral duplication (UD) is a rare congenital anomaly with multiple anatomical variants. CASE PRESENTATION In this article we present a four year-old child with complete UD. The patient was admitted for hypospadias repair, in evaluation we found type IIA1 UD according to Effmann classification. Patient underwent hypospadias repair saving complete UD. CONCLUSIONS After one year follow-up he has normal and continent urination.
منابع مشابه
Novel Presentation of Complete Coronal Urethral Duplication: a Case Report
Urethralduplication is a rare condition occurs as a congenital malformation either independently or in the setting of other congenital malformations such as caudal duplication syndrome. Its prevalence becomes even rarer if it manifests as two side-by-side tracts in coronal plan.Nonetheless, we introduce a unique presentation of complete coronal urethral duplication accompanied by astoundin...
متن کاملComplete colonic duplication in children
Background: Complete colonic duplication is a very rare congenital anomaly that may have different presentations according to its location and size. Complete colonic duplication can occur in 15% of gastrointestinal duplication. We report two cases of complete colonic duplications, and their characteristics. Case Presentation: We present two patients with complete colonic duplication with differ...
متن کاملA case of coronal urethral duplication with no other abnormalities.
Urethral duplication is a very rare congenital anomaly. Urethral duplication is seen most commonly in the sagittal plane. We report a rare case of complete urethral duplication in the coronal plane with no other associated anomalies. Surgical correction of this coronal urethral duplication resulted in a normal-appearing penis and good functional outcome with a single midline urethral meatus and...
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 کاملUrethral duplication: a rare cause of urinary incontinence in a female child
Female urethral duplication is a rare congenital anomaly. We report a case of complete urethral duplication along with horseshoe kidney in a four-years-old female child presenting with incontinence since childhood.
متن کامل