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Patients with anorectal malformation and Hirschsprung's disease.
Eur J Pediatr Surg. 2009 Oct; 19(5):325-7.EJ

Abstract

BACKGROUND

Dysganglionosis and aganglionosis have been frequently described in biopsies of the distal bowel in patients with anorectal malformation (ARM). They are interpreted as a developmental disorder of the anorectum. The true association of total colonic aganglionosis and anorectal malformation has not been reported before. The aim of this study was to explore the true association of anorectal malformation and Hirschsprung's disease with or without trisomy 21.

MATERIAL & METHODS

A retrospective study of all patients diagnosed with anorectal malformation in our institute from 1986-2008 was performed. All patients with anorectal malformation and Hirschsprung's disease were included in the study. Rectal biopsies were taken from multiple sites, including the rectum, left, transverse, right colon and appendix. The diagnosis of aganglionosis was proven histopathologically by the absence of ganglion cells with or without acetylcholinesterase staining. Specimens were examined by at least two experienced consultant pathologists.

RESULTS

Aganglionosis was confirmed in three patients out of 53 patients with anorectal malformation. Two had Down's syndrome. All were males and presented with high anorectal malformation without fistula. The clinical presentation was intestinal obstruction, necrotizing enterocolitis and failure to thrive. The level of aganglionosis was up to the left colon in two and total colonic with ileal involvement in one. One of the children with Down's syndrome and total colonic aganglionosis died. Another had correction of a congenital heart disease, colostomy and is awaiting definitive surgery. The third case is continent at the age of 22 years with a Malone stoma after pull-through of ARM and a subsequent Duhamel procedure.

CONCLUSIONS

The association between ARM and intestinal dysganglionosis is not rare. We recommend not using the distal rectal pouch and parts of the fistula in the reconstruction of anorectal malformations as this may solve the constipation if the pathology is limited. In cases of aganglionosis beyond the rectal pouch and fistula, surgical intervention is needed. Delay in diagnosis may lead to morbidity or even mortality.

Authors+Show Affiliations

King Fahd Armed Forces Hospital, Department of Pediatric Surgery, Jeddah, Saudi Arabia. enaamraboei@yahoo.fr

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

19548194

Citation

Raboei, E H.. "Patients With Anorectal Malformation and Hirschsprung's Disease." European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [et Al] = Zeitschrift Fur Kinderchirurgie, vol. 19, no. 5, 2009, pp. 325-7.
Raboei EH. Patients with anorectal malformation and Hirschsprung's disease. Eur J Pediatr Surg. 2009;19(5):325-7.
Raboei, E. H. (2009). Patients with anorectal malformation and Hirschsprung's disease. European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [et Al] = Zeitschrift Fur Kinderchirurgie, 19(5), 325-7. https://doi.org/10.1055/s-0029-1224131
Raboei EH. Patients With Anorectal Malformation and Hirschsprung's Disease. Eur J Pediatr Surg. 2009;19(5):325-7. PubMed PMID: 19548194.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Patients with anorectal malformation and Hirschsprung's disease. A1 - Raboei,E H, Y1 - 2009/06/22/ PY - 2009/6/24/entrez PY - 2009/6/24/pubmed PY - 2010/1/20/medline SP - 325 EP - 7 JF - European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie JO - Eur J Pediatr Surg VL - 19 IS - 5 N2 - BACKGROUND: Dysganglionosis and aganglionosis have been frequently described in biopsies of the distal bowel in patients with anorectal malformation (ARM). They are interpreted as a developmental disorder of the anorectum. The true association of total colonic aganglionosis and anorectal malformation has not been reported before. The aim of this study was to explore the true association of anorectal malformation and Hirschsprung's disease with or without trisomy 21. MATERIAL & METHODS: A retrospective study of all patients diagnosed with anorectal malformation in our institute from 1986-2008 was performed. All patients with anorectal malformation and Hirschsprung's disease were included in the study. Rectal biopsies were taken from multiple sites, including the rectum, left, transverse, right colon and appendix. The diagnosis of aganglionosis was proven histopathologically by the absence of ganglion cells with or without acetylcholinesterase staining. Specimens were examined by at least two experienced consultant pathologists. RESULTS: Aganglionosis was confirmed in three patients out of 53 patients with anorectal malformation. Two had Down's syndrome. All were males and presented with high anorectal malformation without fistula. The clinical presentation was intestinal obstruction, necrotizing enterocolitis and failure to thrive. The level of aganglionosis was up to the left colon in two and total colonic with ileal involvement in one. One of the children with Down's syndrome and total colonic aganglionosis died. Another had correction of a congenital heart disease, colostomy and is awaiting definitive surgery. The third case is continent at the age of 22 years with a Malone stoma after pull-through of ARM and a subsequent Duhamel procedure. CONCLUSIONS: The association between ARM and intestinal dysganglionosis is not rare. We recommend not using the distal rectal pouch and parts of the fistula in the reconstruction of anorectal malformations as this may solve the constipation if the pathology is limited. In cases of aganglionosis beyond the rectal pouch and fistula, surgical intervention is needed. Delay in diagnosis may lead to morbidity or even mortality. SN - 1439-359X UR - https://www.unboundmedicine.com/medline/citation/19548194/Patients_with_anorectal_malformation_and_Hirschsprung's_disease_ L2 - http://www.thieme-connect.com/DOI/DOI?10.1055/s-0029-1224131 DB - PRIME DP - Unbound Medicine ER -