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Surgical Management of Meatal Stenosis with Meatoplasty
Published on: November 30, 2010
Individualized management of upper rectal atresia
Chih-Cheng Luo1, Yung-Ching Ming, Shih-Ming Chu
1Department of Pediatric Surgery, Chang Gung Children's Medical Center, Chang Gung University College of Medicine, Taoyuan 333, Taiwan. a72001234@yahoo.com.tw
Insights
Congenital colonic atresia (CA) is a rare cause of neonatal intestinal obstruction. This study highlights transanal mucosectomy as a useful technique for upper rectal atresia, emphasizing individualized surgical approaches.
Area of Science:
- Pediatric Surgery
- Neonatal Gastroenterology
- Congenital Malformations
Background:
- Congenital colonic atresia (CA) or stenosis is a rare cause of low intestinal obstruction in neonates.
- Management of CA depends on the atretic site and associated anomalies.
- This study focuses on the experience with upper rectal atresia.
Purpose of the Study:
- To report the clinical experience with upper rectal atresia over a 5-year period.
- To analyze clinical presentation, diagnosis, management, and outcomes.
- To evaluate surgical techniques for upper rectal atresia.
Main Methods:
- Retrospective analysis of 3 female newborns with upper rectal atresia treated between 2004 and 2008.
- Review of clinical presentation, diagnostic methods, associated anomalies, surgical techniques, and outcomes.
- Evaluation of contrast enema, laparotomy findings, and surgical procedures.
Main Results:
- All 3 patients presented with abdominal distension, bilious vomiting, and failure to pass meconium.
- Two patients showed upper rectal atresia on contrast enema; laparotomy confirmed Type III atresia in one.
- Surgical management included sigmoid colostomy, transanal mucosectomy, and pull-through procedures; one patient had associated jejunoileal atresias and imperforate anus with complications.
Conclusions:
- Upper rectal atresia is an uncommon condition requiring individualized surgical management.
- Transanal mucosectomy is a valuable technique for definitive pull-through procedures.
- Missed diagnosis of upper rectal atresia, especially with imperforate anus, can lead to delayed diagnosis and complications.
Background/Purpose:
Congenital colonic atresia (CA) or stenosis is an infrequent cause of low intestinal obstruction in the neonate. Atresias can occur at any level, and the management of CA is determined by the atretic site and by the presence or absence of associated anomalies. We report our experience dealing with upper rectal atresia during a 5-year period.
Methods:
Between January 2004 and December 2008, 3 female newborns with upper rectal atresia with or without associated anomalies were treated. Modes of clinical presentation, methods of diagnosis, associated anomalies, alternative management techniques, and clinical outcome were retrospectively analyzed.
Results:
All 3 patients had progressive abdominal distension, bilious vomiting, and failure to pass meconium. Contrast enema showed an atresia at the upper rectum in 2 patients. At laparotomy, case 1 was found to have type III atresia of the upper rectum. Resection of the dilated portion of the proximal colon with end sigmoid colostomy was accomplished in the neonatal period followed by a transanal mucosectomy with takedown of the colostomy and a pull-through procedure at age 3 months. Case 3 had multiple jejunoileal atresias and an upper rectal atresia. The initial management was multiple resections of atretic bowel and anastomoses and an end sigmoid colostomy. The secondary procedure was a takedown of the colostomy and transanal mucosectomy with a pull-through procedure. Case 2 had type I upper rectal atresia in association with imperforate anus complicated by colon perforation during performance of a distal colostogram leading to a complicated and protracted clinical course. All the patients are currently well with voluntary bowel movements, and one has occasional soiling with follow-up of 9 months to 3 years.
Conclusions:
Colon atresia, especially at the level of the upper rectum, is uncommon. Whether to proceed with an ostomy or to individualize the operative procedure according to the location of the atresia is still controversial. Transanal mucosectomy was a useful technique at the time of the definitive pull-through for the treatment of upper rectal atresia. In cases of upper CA associated with imperforate anus, delay in diagnosis and potential complications may result if the diagnosis of upper rectal atresia is missed.
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