Affiliation:
1. Alexandria University
2. Tanta Faculty of Medicine
Abstract
Abstract
Introduction: Rectal atresia is a rare subtype of anorectal malformations in which the patients are born with a normal anal canal but have complete atresia located few centimeters proximal to the dentate line. We present the transanal end-to-end rectoanal anastomosis as a surgical technique for the management of these patients, highlight the outcomes, and emphasize on some clinical tips.
Methods: Four patients were diagnosed as having rectal atresia on clinical and radiological basis. All of them underwent single loop low sigmoid colostomy in the first 24 hours. After 6 months, transanal end-to-end rectoanal anastomosis was performed followed by closure of the stoma 3 months later.
Results: The 2 cases that are older than 3 years demonstrated normal continence and are clean between bowel movements, while the other two showed good anal tone and passing stools between 1–3 times daily, being dry in between.
Conclusion: Transanal end-to-end rectoanal anastomosis allows a safer route of anatomical reconstruction of the anorectum, therefore avoiding the potential complications associated with the other more invasive approaches.
Publisher
Research Square Platform LLC
Reference16 articles.
1. Anorectal malformations;Pena A;Semin Pediatr Surg,1995
2. Dorairajan T. Anorectal atresia. In: Stephens FD, Smith ED, Paul NW, editors. Anorectal malformations in children. New York: Liss; 1988. pp. 105–10.
3. Transanal endoscopic-assisted proctoplasty—a novel surgical approach for individual management of patients with imperforate anus without fistula;Pakarinen MP;J Pediatr Surg,2006
4. Congenital Rectal Atresia: Which Surgical Approach?;Al-Salem A;J Pediatr Surg Specialties,2017
5. Rectal atresia and anal stenosis: the difference in the operative technique for these two distinct congenital anorectal malformations;Lane VA;Tech Coloproctol,2016