| ORIGINAL ARTICLE
|Year : 2021 | Volume
| Issue : 3 | Page : 153-161
Congenital pouch colon: Case series and review of evidences for resection
Miriam Duci1, Francesco Fascetti-Leon1, Enrico La Pergola2, Paola Midrio3, Piergiorgio Gamba1
1 Department of Salute della Donna e del Bambino, Division of Pediatric Surgery, University of Padova, Padova, Italy
2 Department of Pediatric Surgery, Vittore Buzzi Children Hospital, Milano, Lombardia, Italy
3 Mother and Child Department, Pediatric Surgery Unit, “Cà Foncello Hospital” Treviso, Treviso, Italy, Italy
Background: Congenital pouch colon (CPC) is a rare variant of anorectal malformations (ARM) with its highest reported incidence in India. We aimed to describe five patients affected by CPC, in which the tissue from the terminal dilated colon has been successfully used and to discuss our results on the light of an extended revision of the literature.
Materials and Methods: The clinical details of five cases treated for CPC in two Italian Centers were retrospectively reviewed assessing the fate of the terminal dilated colon.
Results: In all cases, the tissue from dilated colon has been used. The double vascular system of the dilated pouch allowed increasing bladder capacity (case 4), reconstruction of the vagina (case 3, 5), and lengthening of the colon (case 1, 2, 5). In our series, 3/5 have a good bowel control with daily bowel management after ARM correction. In literature, there are not differences in terms of dependence from bowel management in patients with pouch resected and in patients with pouch saved (P = 0.16).
Conclusions: We acknowledge that the analysis of the available literature is limited by the absence of studies with high level of evidence and the removal or the preservation of the abnormal colon tissue seems to follow the surgeon preferences.
Dr. Francesco Fascetti-Leon
Department of Women's and Children's Health, Division of Paediatric Surgery, University of Padova, Via Giustiniani 2, Padua 35128
Source of Support: None, Conflict of Interest: None
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