Eur J Pediatr Surg 2009; 19(4): 254-255
DOI: 10.1055/s-2008-1038882
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© Georg Thieme Verlag KG Stuttgart · New York

Isolated Diphallia: Case Report and Literature Review

S. Keckler1 , H. A. Stephany1 , T. L. Spilde1 , C. L. Snyder1
  • 1Department of Surgery, Children's Mercy Hospital, Kansas City, Missouri, USA
Further Information

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

  • 1 Aleem A A. Diphallia: a report of a case.  J Urol. 1973;  108 357
  • 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