Abstract
Purpose
Colonic atresia is a rare cause of congenital intestinal obstruction in the neonate. A review of the management and outcome of children with colonic atresia was performed.
Methods
A retrospective analysis of the complete records of children treated for colonic atresia during the 30-year period.
Results
A total of 14 newborns were treated. Seven infants suffered from an isolated colonic atresia (group 1). In the other seven infants (group 2), colonic atresia was either associated with additional intestinal atresias (n = 2), or gastroschisis (n = 5). Gestational age and birth weight were significantly lower in infants from group 2 compared to group 1 (40 ± 0.5 vs. 37 ± 1 weeks (P < 0.05); and 3,478 ± 208 vs. 2,626 ± 242 g (P < 0.01), respectively). The first surgical procedure was performed in all newborns within 24 h after birth. All but one infant from group 1 received primary colostomies at the level of colonic atresia, followed by end-to-side anastomoses. All but one infant from group 2 needed ileocoecal resection due to bowel necrosis. No child died in group 1, whereas three children died in group 2.
Conclusions
Isolated colonic atresia is amenable with a short hospital stay and an excellent outcome. In contrast, infants with colonic atresia associated with gastroschisis present a serious clinical challenge.
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References
Webb CH, Wangsteen OH (1931) Congenital intestinal atresia. Am J Dis Child 41:262–284
Snyder CL, Miller KA, Sharp RJ, Murphy JP, Andrews WA, Holcomb GW 3rd, Gittes GK, Ashcraft KW (2001) Management of intestinal atresia in patients with gastroschisis. J Pediatr Surg 36:1542–1545
Fleet MS, de la Hunt MN (2000) Intestinal atresia with gastroschisis: a selective approach to management. J Pediatr Surg 35:1323–1325
Gornall P (1989) Management of intestinal atresia complicating gastroschisis. J Pediatr Surg 24:522–524
Collins DL, Kimura K, Morgan A, Johnson DG, Leonard C, Jones MC (1986) Multiple intestinal atresia and amyoplasia congenita in four unrelated infants: a new association. J Pediatr Surg 21:331–333
De Lorimier AA, Hyde GA (1968) Colon atresia and Hirschsprung’s disease. Surgery 64:976–978
Haffner JFW, Schistad G (1969) Atresia of the colon combined with Hirschsprung’s disease. J Pediatr Surg 4:560–562
Akgur F, Tanyel FC, Buyukpamukcu N, Hicsonmez A (1993) Colonic atresia and Hirschsprung’s disease association shows further evidence for migration of enteric neurons. J Pediatr Surg 28:635–636
Williams MD, Burrington JD (1993) Hirschsprung’s disease complicating colon atresia. J Pediatr Surg 28:637–639
Kim PCW, Superina RA, Ein S (1995) Colonic atresia combined with Hirschsprung’s disease: a diagnostic and therapeutic challenge. J Pediatr Surg 30:1216–1217
Szavay PO, Schliephake H, Hubert O, Glüer S (2002) Colon atresia, facial hemiaplasia, and anophthalmia: a case report. J Pediatr Surg 37:1498–1500
Hitchcock R, Birthistle K, Carrington D, Calvert SA, Holmes K (1995) Colonic atresia and spinal cord atrophy associated with a case of fetal varicella syndrome. J Pediatr Surg 30:1344–1347
Goodwin S, Schlatter M, Connors R (2006) Imperforate anus and colon atresia in a newborn. J Pediatr Surg 41:583–585
Etensel B, Temir G, Karkiner A, Melek M, Edirne Y, Karaca I, Mir E (2005) Atresia of the colon. J Pediatr Surg 40:1258–1268
Pohlson EC, Hatch EI, Glick PL, Trapper D (1988) Individualised management of colonic atresia. Am J Surg 155:690–692
Watts AC, Sabharwal AJ, MacKinlay GA, Munro FD (2003) Congenital colonic atresia: should primary anastomosis always be the goal? Pediatr Surg Int 19:14–17
Gregersen N (2006) Facial asymmetry with colon atresia. Clin Dysmorphol 15:45–46
Grosfeld JL, Ballantine TV, Shoemaker R (1979) Operative mangement of intestinal atresia and stenosis based on pathologic findings. J Pediatr Surg 14:368–375
Bianchi A (1980) Intestinal lengthening: a technique for increasing small intestinal length. J Pediatr Surg 15:145–151
Karnak I, Çiftçi AO, Senocak ME, Tanyel FC, Büyükpamukçu N (2001) Colonic atresia: surgical management and outcome. Pediatr Surg Int 17:631–635
Coran AG, Eraklis AJ (1969) Atresia of the colon. Surgery 65:828–831
Cox SG, Numanoglu A, Millar AJ, Rode H (2005) Colonic atresia: spectrum of presentation and pitfalls in management. A review of 14 cases. Pediatr Surg Int 21:813–818
Benson CD, Lofti MW, Brough AJ (1968) Congenital atresias and stenosis of the colon. J Pediatr Surg 3:253–257
DeFore WW Jr, Garcia-Rinaldi R, Mattox K, Harberg FJ (1976) Surgical management of colon atresia. Surg Gynecol Obstet 143:767–769
Powell RW, Raffensperger JG (1982) Congenital colonic atresia. J Pediatr Surg 17:166–170
Davenport M, Bianchi A, Doig CM, Gough CS (1990) Colonic atresia: current results of treatment. J R Coll Surg Edin 35:25–28
Reid GM (2006) Sudden infant death syndrome (SIDS): microgravity and inadequate sensory stimulation. Med Hypotheses 66:920–924
Louw JH, Barnard CN (1955) Congenital intestinal atresia: observations on its origin. Lancet 2:1065–1067
Hove HD, Bisgaard AM, Nissen KR, Kirchhoff M (2008) Facial asymmetry associated with small and large intestinal atresia, and ipsilateral malformations of eye, skin, and extremities. Clin Dysmorphol 17:121–122
Boles ET Jr, Vassy LE, Ralston M (1976) Atresia of the colon. J Pediatr Surg 11:69–75
Puri P, Fujimoto T (1988) New observations on the pathogenesis of multiple intestinal atresias. J Pediatr Surg 23:221–225
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Haxhija, E.Q., Schalamon, J. & Höllwarth, M.E. Management of isolated and associated colonic atresia. Pediatr Surg Int 27, 411–416 (2011). https://doi.org/10.1007/s00383-010-2802-3
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DOI: https://doi.org/10.1007/s00383-010-2802-3