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DOI: 10.1055/s-2008-1038882
© Georg Thieme Verlag KG Stuttgart · New York
Isolated Diphallia: Case Report and Literature Review
Publication History
received April 14, 2008
revised June 27, 2008
accepted July 10, 2008
Publication Date:
08 May 2009 (online)
Introduction
Diphallia (also known as penile duplication or diphallasparatus) is a rare malformation with an estimated frequency of one case per five million births and is commonly associated with duplications or malformations of the urinary tract, anorectal and vertebral malformations. It is an extremely rare disorder with only approximately 100 such cases of diphallus reported throughout the world [5]. We report a case of true diphallia without associated urinary or anorectal malformations.
References
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- 2 Bhat H S, Sukumar S, Nair T P. et al . Successful surgical correction of true diphallia, scrotal duplication, and associated hypospadias. J Pediatr Surg. 2006; 41 E13-E14
- 3 Cohen S J. Diphallus with duplication of colon and bladder. Proc R Soc Med. 1968; 61 305
- 4 Djordjevic M L, Perovic S V. Complex penile joining in a case of wide penile duplication. J Urol. 2005; 173 587-588
- 5 Gyftopoulus K, Wolffenbuttel K P, Nijman R J. Clinical and embryologic aspects of penile duplications and associated anomalies. Urology. 2002; 60 675
- 6 Johnson C F, Carlton Jr C E, Powell N B. Duplication of penis. Urology. 1974; 6 722-725
- 7 Marti-Bonmati L, Menor F, Gomez J, Cortina H, Garcia Ibarra F. Value of sonography in true complete diphallia. J Urol. 1989; 142 356-357
Dr. M.D. Scott Keckler
Department of Surgery
Children's Mercy Hospital
2401 Gillham Rd
Kansas City, MO 64108
USA
Email: skeckler1@cmh.edu