Complete diphallia: How to proceed?
Diphallia
Penile malformation
Reconstructive surgery
Journal
Journal of pediatric urology
ISSN: 1873-4898
Titre abrégé: J Pediatr Urol
Pays: England
ID NLM: 101233150
Informations de publication
Date de publication:
06 2022
06 2022
Historique:
received:
25
10
2021
revised:
02
02
2022
accepted:
25
02
2022
pubmed:
30
3
2022
medline:
29
6
2022
entrez:
29
3
2022
Statut:
ppublish
Résumé
Diphallia is a rare anomaly. It has a range of appearances from a small accessory penile to complete duplication. We present a 2 year-old boy with complete penile duplication. The left penile was the largest. NMR (Nuclear Magnetic Resonance) suggested one corporal body for each penile and VCUG (Voiding Cystourethrogram) showed a normal urethra in the right penile and stricture at glandular and mid penile urethra of the left penis. A Y confluence to bulbar urethra was observed confirming only one prostate and bladder. The cystoscopy through the right penile identified the urethral confluence in the bulbar area. We performed a meatotomy in the left penile to insert the cystoscope and confirmed the blind ending urethra. We decided to remove this penile. The penile was degloved entirely and clamped and took out the corpora at the base. Diphallia can have three presentations: only glans duplication, bifid diphallia and complete diphallia (two corpora cavernosa and a corpus spongiosum for each penile). In our case, each penile presented only one corpora cavernosa and the decision taken was based on urethral patency. The treatment should always be planned individually whereas associated anomalies with the goal of attaining satisfactory functional and cosmetic results.
Identifiants
pubmed: 35346592
pii: S1477-5131(22)00093-6
doi: 10.1016/j.jpurol.2022.02.026
pii:
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
399-400Informations de copyright
Copyright © 2022 Journal of Pediatric Urology Company. Published by Elsevier Ltd. All rights reserved.