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Published on: November 30, 2010
Rectal atresia: pathogenesis and operative treatment
C Festen1, R S Severijnen, F H van der Staak
1Department of Pediatric Surgery, P. O. Box 9101, NL-6500, HB Nijmegen, The Netherlands.
Pediatric Surgery International
|September 24, 2013
Summary
Rectal atresia (RA) is a rare condition. This study suggests RA may occur with other congenital anomalies, challenging the idea it is always acquired. Surgical treatment showed good outcomes.
Area of Science:
- Pediatric Surgery
- Congenital Malformations
- Gastrointestinal Surgery
Background:
- Rectal atresia (RA) is a rare anorectal malformation.
- It is often considered an acquired lesion due to vascular genesis.
- The absence of other congenital anomalies is cited as evidence for acquired etiology.
Purpose of the Study:
- To investigate the association between rectal atresia and other congenital anomalies.
- To evaluate the etiology of rectal atresia.
- To report surgical outcomes for rectal atresia.
Main Methods:
- Case series of four patients with rectal atresia and associated congenital anomalies.
- Literature review of two additional cases.
- Surgical treatment using the posterior sagittal approach.
Main Results:
- Four new cases of rectal atresia with significant congenital anomalies were identified.
- Two similar cases were found in existing literature.
- All patients treated with the posterior sagittal approach achieved good functional results.
Conclusions:
- The presence of other congenital anomalies in rectal atresia cases challenges the theory of an exclusively acquired etiology.
- Rectal atresia may have a congenital component.
- The posterior sagittal approach is effective for treating rectal atresia.

