Complete diphallia: How to proceed?

被引:3
|
作者
Macedo Jr, Antonio [1 ,2 ]
Ottoni, Sergio Leite [2 ]
Barros Camilato, Paula Cartaxo [2 ]
Crespo Ganchozo, Hugo Santiago [2 ]
Garrone, Gilmar [2 ]
Marcondes, Ricardo de Mattos [2 ]
da Cruz, Marcela Leal [2 ]
机构
[1] Univ Fed Sao Paulo, Dept Pediat, Sao Paulo, Brazil
[2] CACAU NUPEP, Dept Urol, Sao Paulo, Brazil
关键词
Diphallia; Penile malformation; Reconstructive surgery;
D O I
10.1016/j.jpurol.2022.02.026
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction Diphallia is a rare anomaly. It has a range of appearances from a small accessory penile to complete duplication. Methods 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. Results 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. Discussion 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. Conclusion The treatment should always be planned individually whereas associated anomalies with the goal of attaining satisfactory functional and cosmetic results.
引用
收藏
页码:399 / 400
页数:2
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