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Caudal duplication syndrome: Complete duplication of the hindgut and genitourinary system

Authors :
Mohammad Alomar
Hussam Dalati
Yasser Mustafa
Khaled Othman
Source :
Journal of Pediatric Surgery Case Reports, Vol 66, Iss, Pp 101789-(2021)
Publication Year :
2021
Publisher :
Elsevier, 2021.

Abstract

Caudal duplication syndrome is a very rare anomaly and poses a major challenge for surgeons. The term caudal duplication syndrome is used to describe the association between hindgut duplication, duplication of the genitourinary, and malformations of the spinal cord and vertebrae. A 5-year-old girl is reported with complete duplication of the entire large bowel, cecum, appendix, about 2 cm of the terminal ileum, bladder, urethra, vagina, uterus, and vertebral body deformities. After an extensive evaluation phase, a laparotomy was performed and the duplicated colon was excised completely without removing the adjacent native colon.

Details

Language :
English
ISSN :
22135766
Volume :
66
Database :
OpenAIRE
Journal :
Journal of Pediatric Surgery Case Reports
Accession number :
edsair.doi.dedup.....d2a80aba0b3bb8d012d46a4191ae5cee