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Single-stage Reconstruction in a Rare Case of Female Caudal Duplication Syndrome
Nilesh Tank1, Aroon Trivedi1, Tharanendran Heera2
1Department of Pediatric Surgery, UNM Childrens Hospital, Surat, Gujarat, India.
Abstract:
Caudal duplication syndrome is exceptionally rare. We report a female infant with complex genitourinary and colorectal duplication managed by detailed imaging and single-stage definitive reconstruction. Excision of nonfunctional duplicated organs, transureteroureterostomy, bowel reconstruction, and perineal unification achieved good urinary, bowel, and cosmetic outcomes at short-term follow-up without significant complications.
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