Complete diphallia – Our technique to avoid complications

Deshpande, Vidyanand

doi:10.4103/jiaps.jiaps_76_19

Cited by 2 publications

(1 citation statement)

References 3 publications

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“…We did posterior sagittal anorectoplasty and excision of left penis and perineal lipoma with reconstruction of scrotum in second stage of procedure. Amputation of accessory penis along with urethral endto-side anastomosis in anterior urethra can be an option as done by some, we only remove the accessory penis with closer of urethral stump close to its bifurcation from main right urethra as in Fig 2, we can see that the course of right urethra is straight, left urethra is looking as originate as a branching from right main urethra below bladder neck [13,14]. On review of the literature, we did not come across any other case of this variety of the penile duplication with anorectal malformations.…”

Section: Theory Suggested By Hollowell Et Al Diphallia Resultsmentioning

confidence: 99%

An extremely rare case of diphallia with high anorectal malformation with perineal lipoma

Rawat¹,

Singh²,

Pant³

et al. 2021

j-pucr

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Section: Theory Suggested By Hollowell Et Al Diphallia Resultsmentioning

confidence: 99%

An extremely rare case of diphallia with high anorectal malformation with perineal lipoma

Rawat¹,

Singh²,

Pant³

et al. 2021

j-pucr

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Diphallia: literature review and proposed surgical classification system

Kendrick

Kimble

2022

ANZ Journal of Surgery

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Background Diphallia occurs once in 5–6 million births, with no two patients presenting with the same anatomical variation. Here we discuss a review of diphallia case reports, as well as present a new surgical classification system based on the soft tissue composition of the two phalluses, the anatomy of the urethra present within the most normal phallus and the bladder configuration. Methods Eighty‐seven diphallia case reports were collected and analysed, excluding those presented in animals and articles that were non‐English, with the results compiled to provide an in‐depth reference of the specific anatomy found in diphallia patients and the associated abnormalities. Results Our proposed classification system was then applied to each patient and the most common configuration base on our classification system presented, along with commonly seen associated anomalies. Conclusion The reviewed cases represent a subset of the most unique diphallia patients; thus, several cases may be left unreported. Future reports can then be categorized, aiding as a reference, and potentially building on the classification, should the patient not fit into a specific group, leading to an expansion of the classification system.

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Complete diphallia – Our technique to avoid complications

Cited by 2 publications

References 3 publications

An extremely rare case of diphallia with high anorectal malformation with perineal lipoma

An extremely rare case of diphallia with high anorectal malformation with perineal lipoma

Diphallia: literature review and proposed surgical classification system

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