Duplications sagittales antérieures de l'urètre chez le garçon. À propos d'un cas

Bouhafs, A.; Abarchi, H; Belkacem, Rachid; Barahioui, M.

doi:10.1016/s0003-4401(01)00088-2

Cited by 4 publications

(4 citation statements)

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“…The association with other anomalies of the upper urinary tract is rare. Genito-urinary malformations (renal dysplasia, vesicoureteral reflux, bladder exfoliation, cryptorchidia), digestive and musculoskeletal disorders have been described [2,7]. This is the case of our observation No.…”

Section: Discussionsupporting

confidence: 52%

“…The ventral urethra emerging from the bladder opens from the region of the glans to the penoscrotal region. The ventral urethra is always the most functional of the two, although the dorsal urethra is the only one in the normal position [1,2]. The age of discovery is precocious, usually, before the age of one year [2], a case of our patients was diagnosed at 24 months.…”

Section: Discussionmentioning

confidence: 87%

“…It is defined by the juxtaposition of 2 or more channels with smooth muscular structure with a mucosal coating of excreto-urinary type [2]. It can be complete or incomplete [3].…”

Section: Introductionmentioning

confidence: 99%

“…It can be complete or incomplete [3]. It occurs preferentially in the sagittal plane but also in the frontal plane [2]. Numerous anatomical varieties have been described with a second urethra opening in standard position or not.…”

Section: Introductionmentioning

confidence: 99%

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Urethral duplication in male children's: report of four cases

Bakkaly¹,

Amiry²,

Lafia³

et al. 2018

Int J Surg Med

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Objective: To evaluate the medium-term outcomes of the management of children with urethral duplication. Materials and Methods: We report a retrospective study of four children carrying urethral duplication followed in our department over a period of 5 years from 2010 to 2015; Preoperative exploration was based on ultrasound, urethrocystography retrograde and the fistulography. Results: In our study, three patients had rare form of epispadias urethral duplication (complete type II of Effmann and Leibowitz) and one, a "Y" duplication (type II A2). We proceeded in all cases, to the resection of a super urethra excision. The follow up was from 6 months to 2 years for our patients. There was no infectious complication. For one patient with Y urethral duplication, a stenosis of the path of the dorsal urethra was preserved within complete urination. Conclusion: Urethral duplication on a boy is a rare anomaly of the urinary tract. The diagnosis and the determination of its type are based on the retrograde cystography. Its varied clinical expression depends on its anatomical type. If the diagnosis is established in a symptomatic context, the surgical indication is posed with good performances in most cases.

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Section: Discussionsupporting

confidence: 52%

Section: Discussionmentioning

confidence: 87%

“…It is defined by the juxtaposition of 2 or more channels with smooth muscular structure with a mucosal coating of excreto-urinary type [2]. It can be complete or incomplete [3].…”

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

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