Rectal atresia: a rare cause of failure to pass meconium
Fatima Zahrae Laamrani, Rachida Dafiri
Corresponding author: Fatima Zahrae Laamrani, Radiology Department, Children’s Hospital, Rabat, Morocco
Received: 19 Feb 2014 - Accepted: 10 Apr 2014 - Published: 24 Oct 2014
Domain: Maternal and child health
Keywords: Rectal-atresia, failure to pass meconium, anorectal malformation
©Fatima Zahrae Laamrani et al. Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Fatima Zahrae Laamrani et al. Rectal atresia: a rare cause of failure to pass meconium. Pan African Medical Journal. 2014;19:198. [doi: 10.11604/pamj.2014.19.198.4057]
Available online at: https://www.panafrican-med-journal.com//content/article/19/198/full
Rectal atresia: a rare cause of failure to pass meconium
Fatima Zahrae Laamrani1,&, Rachida Dafiri1
1Radiology Department, Children’s Hospital, Rabat, Morocco
&Corresponding author
Fatima Zahrae Laamrani, Radiology Department, Children’s Hospital, Rabat, Morocco
Rectal atresia or stenosis is an extremely rare anorectal malformation associating a normal anal canal with a stricture or a complete rectal atresia. We describe a case of rectal atresia in a newborn female presenting with an abdominal distension and failure of passing meconium.
Rectal atresia is a rare anorectal malformationcombining a normally developed anus and an atretic rectal segment. A failure to pass meconium in a new born with normal present anus must lead to further clinical and radiologic investigations which findings are specific (Table 1).
A twenty-day-old female child was admitted with a history of chronic vomiting, not passing meconium since birth and a progressive abdominal distension. The perineal examination objectified a normally placed anus with no perineal fistula. When introducing a thermometerper rectum, it stops at 2 cm from the anal verge with no explosive stools. Abdominal x–raysshowed a massively distended colon with pelvic emptiness (Figure 1). A barium enema was performed, showing an atretic inferior rectal segment with a superior rectal pouch and no fistula (Figure 2). An end to end anastomosis after a posterior sagittal anorectoplasty was performed with a satisfying evolution.
Etiology and demographics
Rectal atresia is a rare anorectal anomaly combining a normally developed anus and an atretic rectal segment representing 1-2% of all anorectal anomalies. Rectal atresia is considered separate from imperforate anus or anal atresia because, in rectal atresia, the anus is present and normal, but a variable rectal segment is atretic. Incomplete rectal atresia refers to complete membrane or severe stenosis. An in utero ischemic accident seems to explain the pathogenesis of this rectal malformation [1, 2].
Clinical and imaging findings
Failure to pass meconium, progressive abdominal distention, refusal to feed and vomiting suggest the intestinal obstruction in neonates and lead to further investigations [3]. The clinical diagnosis is easy to confirm. When passing per rectum a firm catheter of size 8 or 10 stops at 2-3 cm from the anal verge [4]. After a rectal atresia is clinically identified, radiography must be performed and usually shows a colonic obstruction. Barium enema shows the rectum with its proximal blinded pouch and the atretic segment which may interest any part of the rectum [5]. Perineal ultrasonography and magnetic resonance imaging can be used to check preoperatively the exact relation between the anal canal and sphincters. They provide identification of both rectal pouch and sphincteric muscles without ionizing radiation risks [6].
Treatment and prognosis
The extensive list of creative operative procedures used for the rectal atresia reflects the great difficulty faced in treating this anomaly. Optimal continence remains the crucial goal in the treatment of all forms of anorectal anomalies including rectal atresia in which the anal canal and sphincter are normally formed. Continence should be normal after reconstruction.Chronic constipation represents a common postoperative feature [1].
Differential diagnoses (Table 2)
Differential diagnoses include all conditions associated to a low intestinal obstruction manifesting as a neonatalfailure to pass meconium: Hirschsprung’s disease, meconium ileus, colonic atresia, small left colon syndrome, megacystis-microcolon-intestinal hyperperistaltism syndrome , anal atresia and all other anorectal malformations. Clinical and radiologic findings are specific and lead to positive diagnosis of rectal atresia [3].
Rectal atresia is a rare anorectal anomaly combining a normally developed anus and an atretic rectal segment.Failure to pass meconium suggest the intestinal obstruction in neonates. Barium enema shows the rectum with its proximal blinded pouch and the atretic segment.
The authors declare no competing interest.
All authors read and agreed to the final version of this manuscript and equally contributed to its content and to the management of the case.
Table 1: summary table of rectal atresia
Table 2: table of differential diagnoses of rectal atresia
Figure 1: a twenty-day-old female child with a failure to pass to meconium. Technique and findings: Abdominal x–rays shows a massively distended colon with pelvic emptiness
Figure 2: a twenty-day-old female child with a failure to pass to meconium. Technique and findings: Image from a barium enema study shows an atretic inferior rectal segment (arrow) with a superior rectal pouch with no fistula
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