Surgical treatment of penile duplication

Oliveira, Manuel Castanheira de; Ramires, Ricardo; Soares, José; Carvalho, António P. O.; Marcelo, Filinto

doi:10.1016/j.jpurol.2010.01.017

Cited by 13 publications

(25 citation statements)

References 4 publications

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“…Reports of successful surgical procedures for diphallia are few, as it is a rare anomaly. 7,8 In the present case, the urethra of the resected penis was opened to the perineal skin, so as to enable access to the native bladder in case of possible future complication, such as infection or malignant disease.…”

Section: Discussionmentioning

confidence: 99%

Urinary reconstruction in vertebral, anorectal, cardiac, trachea‐esophageal, renal abnormalities and limb defects association with chronic renal failure and penile duplication

et al. 2014

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Abbreviations & AcronymsAbstract: Various urological complications in VATER association require careful management. A 15-year-old boy with VATER association, including a hypoplastic lower urinary tract and diphallia, presented with chronic kidney disease and incontinence after a right loop ureterostomy. In order to acquire urinary continence without renal function impairment, an ileocecal reservoir with umbilical catheterizable stoma was created as a urinary reconstruction. The ectopic posterior penis was resected for cosmetic reasons, and the stump of the hypoplastic urethra was opened at the perineal skin. Clean intermittent selfcatheterization through the umbilicus using disabled bilateral limbs was then achieved. This report describes the management of VATER association in a patient with complicated urological anomalies.

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Section: Discussionmentioning

confidence: 99%

Urinary reconstruction in vertebral, anorectal, cardiac, trachea‐esophageal, renal abnormalities and limb defects association with chronic renal failure and penile duplication

et al. 2014

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“…Excision of ectopic penis was reported in many bodies of literature [6, 15, 20, 22, 23]. Priyadarshi and Djordjevic et al reported penis reconstruction by joining the corporal bodies in each penis in a patient with true complete diphallia [2, 17, 24].…”

Section: Discussion and Literature Reviewmentioning

confidence: 99%

“…The first case was reported in 1609 by Wecker in Bologna, Italy [4, 5]. Until today, only about 100 cases are reported in the literature [4–6]. In Indonesia, this case was never reported.…”

Section: Introductionmentioning

confidence: 99%

Diphallia with Associated Anomalies: A Case Report and Literature Review

Tirtayasa

Prasetyo

Rodjani

2013

Case Reports in Urology

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Diphallia or penile duplication is an extremely rare congenital anomaly. It occurs once in every 5.5 million live births. The extent of penile duplication and the number of associated anomalies vary greatly, ranging from a double glans from a penis with no associated anomaly up to complete penile duplication associated with multiple anomalies. Here, we report a 12-year-old boy with complete bifid diphallia associated with bifid scrotum, epispadia, and pubic symphysis diastasis along with a review of the articles pertaining to this anomaly.

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“…Bifid diphallus is a rare genital anomaly with an incidence of 1 per 5,000,000 live births and is usually associated with other malformations [6]. Diphallia can be divided into 3 categories, including duplication of the glans alone, complete diphallia, and bifid diphallia [7].…”

Section: E2mentioning

confidence: 99%

“…When only one corpus cavernosum is present in each penis, the term bifid phallus applies [2]. The embryologic explanation of diphallia is still obscure but may be the result of a duplication of the cloacal membrane [6].…”

Section: E2mentioning

confidence: 99%