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Case Reports in Radiology
Volume 2018, Article ID 3827820, 5 pages
https://doi.org/10.1155/2018/3827820
Case Report

Urethral Duplication with a Cystic Phallic Urethra Associated with a Uterus Didelphys, Partial Agenesis of the Tibia, and an Equinovarus Foot

1Faculty of Medicine and Biomedical Sciences, University of Yaounde I, Yaounde, Cameroon
2Department of Radiology, Yaounde Gynaeco-Obstetric and Pediatric Hospital, Yaounde, Cameroon
3Department of Pediatric Surgery, Yaounde Gynaeco-Obstetric and Pediatric Hospital, Yaounde, Cameroon
4Department of Neonatology, Yaounde Gynaeco-Obstetric and Pediatric Hospital, Yaounde, Cameroon

Correspondence should be addressed to Edwige Kafando; rf.oohay@1002fakive

Received 29 October 2017; Accepted 7 February 2018; Published 12 March 2018

Academic Editor: Vincent Low

Copyright © 2018 Edwige Kafando et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Urethral duplication is a rare congenital malformation, especially in females. It may be associated with complex urogenital malformations, but the association with a cystic phallic urethra and a uterus didelphys is exceptional. We report a case of a newborn with urethral duplication, with the accessory urethra exteriorized by a large cyst, associated with a uterus didelphys and bone malformations. We discuss the clinical, radiographic, and therapeutic aspects as well as a literature review.