Novel Presentation of Complete Coronal Urethral Duplication: a Case Report | ||
| Journal of Pediatric Perspectives | ||
| مقاله 7، دوره 5، شماره 4 - شماره پیاپی 40، تیر 2017، صفحه 4707-4712 اصل مقاله (476.65 K) | ||
| شناسه دیجیتال (DOI): 10.22038/ijp.2017.22681.1895 | ||
| نویسندگان | ||
| Amrollah Salimi1؛ Shervin Rashidinia2؛ Seyed Shahin Eftekhari2؛ Sara Shahmoradi* 2 | ||
| 1Department of Pediatric Surgery of Hazrat Masoume Hospital, Qom University of Medical Sciences, Qom, Iran. | ||
| 2School of Medicine, Qom University of Medical Sciences, Qom, Iran. | ||
| چکیده | ||
| 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. | ||
| کلیدواژهها | ||
| Appendix؛ Child؛ fistula؛ Urethra | ||
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