Novel Presentation of Complete Coronal Urethral Duplication: a Case Report
نویسندگان
1 Department of Pediatric Surgery of Hazrat Masoume Hospital, Qom University of Medical Sciences, Qom, Iran.
2 School of Medicine, Qom University of Medical Sciences, Qom, Iran.
3 School of Medicine, Qom University of Medical Sciences, Qom, Iran.
4 School of Medicine, Qom University of Medical Sciences, Qom, Iran.
doi
10.22038/ijp.2017.22681.1895چکیده
Urethralduplication is a rare condition occurs as a congenital malformation either independently or in the setting of other congenital malformations such as caudal duplication syndrome. Its prevalence becomes even rarer if it manifests as two side-by-side tracts in coronal plan.Nonetheless, we introduce a unique presentation of complete coronal urethral duplication accompanied by astounding manifestations of gastrointestinal malformations different from what is expected for a normal hind gut or caudal duplication syndrome. A 6-year-old boy with complete coronal duplication of urethra along with duplication of appendix, sigmoid and rectum as well as developmental delay, attracted our attention to report.
