Neophalloplasty in boys with aphallia: A systematic review

Summary Objective Aphallia is a rare penile congenital abnormality. The aim of this systematic review was to assess all available literature on neophalloplasty in infancy with an interest in technical alternatives and clinical outcome. Materials and methods We performed a Pubmed search using the ter...

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Veröffentlicht in:Journal of pediatric urology 2016-02, Vol.12 (1), p.19-24
Hauptverfasser: Oliveira, Diego Estevam Gomes, da Cruz, Marcela Leal, Liguori, Riberto, Garrone, Gilmar, Leslie, Bruno, Ottoni, Sérgio Leite, Souza, Geórgia Rubiane, Ortiz, Valdemar, de Castro, Roberto, Macedo, Antonio
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Sprache:eng
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Zusammenfassung:Summary Objective Aphallia is a rare penile congenital abnormality. The aim of this systematic review was to assess all available literature on neophalloplasty in infancy with an interest in technical alternatives and clinical outcome. Materials and methods We performed a Pubmed search using the terms: neophalloplasty, neophallus, and phalloplasty, and selected articles that presented technical alternatives for penile construction in cases of penile dysgenesis, especially aphallia in children and/or adolescents. Results A total of 319 articles were identified in the initial search. Among the different techniques presented in 19 papers collected, we categorized reconstructive procedures into two groups: microsurgical and non-microsurgical techniques. Among the microsurgical techniques, procedures such as the osteocutaneous fibular flap ( n  = 18), the myocutaneous latissimus dorsi flap ( n  = 24), and the radial forearm free flap ( n  = 293) were reported. Among the non-microsurgical techniques, we found a wider range of technical options (6 in total). Most were based on groin, abdominal, and scrotal flaps. Long-term reports on the functionability of the neophallus and psychological aspects of the patients are lacking. Conclusion In assessing recent literature, it seems rational that neophalloplasty should be regarded as the preferred strategy for boys born with aphallia, in opposition to female gender assignment.
ISSN:1477-5131
1873-4898
DOI:10.1016/j.jpurol.2015.10.003