Skip to main content
Top
Published in: Pediatric Surgery International 4/2016

01-04-2016 | Review Article

Established and emerging concepts in Hirschsprung’s-associated enterocolitis

Author: Ankush Gosain

Published in: Pediatric Surgery International | Issue 4/2016

Login to get access

Abstract

Hirschsprung’s disease (HSCR) is a common cause of neonatal bowel obstruction and the approach to diagnosis and surgical treatment is well defined and accepted. Hirschsprung’s-associated enterocolitis (HAEC) remains a frequent cause of pre-operative and post-operative morbidity and mortality, with unchanged treatment guidelines over multiple decades. Recent advances in our understanding of the genetics underlying HSCR have allowed the development of animal models, some of which recapitulate the HAEC phenotype. These animal models, along with recent translational studies, have implicated multiple facets of mucosal immunity and microbiome dysbiosis in the development of HAEC. Here, we will review the established epidemiology, modes of diagnosis and treatment of HAEC. Furthermore, we will explore emerging concepts in the pathogenesis of this disease; including animal models, alterations in mucosal immunity, dysbiosis of the intestinal microbiome, specific genetic susceptibility, and novel treatment modalities.
Literature
1.
go back to reference Hirschspring H (1888) Constipation in newborns due to dilation and hypertrophy of the colon. Jahrbuch Kinderheikunde Hirschspring H (1888) Constipation in newborns due to dilation and hypertrophy of the colon. Jahrbuch Kinderheikunde
2.
go back to reference Raffensperger JG (1987) Hirschsprung’s disease: a historical review. Bull Soc Sci Med Grand Duche Luxemb 124:31–36PubMed Raffensperger JG (1987) Hirschsprung’s disease: a historical review. Bull Soc Sci Med Grand Duche Luxemb 124:31–36PubMed
5.
go back to reference Baxter KJ, Bhatia AM (2013) Hirschsprung’s disease in the preterm infant: implications for diagnosis and outcome. Am Surg 79:734–738PubMed Baxter KJ, Bhatia AM (2013) Hirschsprung’s disease in the preterm infant: implications for diagnosis and outcome. Am Surg 79:734–738PubMed
10.
go back to reference Foster P, Cowan G, Wrenn EL (1990) Twenty-five years“experience with Hirschsprung”s disease. J Pediatr Surg 25:531–534CrossRefPubMed Foster P, Cowan G, Wrenn EL (1990) Twenty-five years“experience with Hirschsprung”s disease. J Pediatr Surg 25:531–534CrossRefPubMed
11.
go back to reference Rescorla FJ, Morrison AM, Engles D et al (1992) Hirschsprung’s disease. Evaluation of mortality and long-term function in 260 cases. Arch Surg 127:934–41 (discussion 941–2) Rescorla FJ, Morrison AM, Engles D et al (1992) Hirschsprung’s disease. Evaluation of mortality and long-term function in 260 cases. Arch Surg 127:934–41 (discussion 941–2)
12.
go back to reference Harrison MW, Deitz DM, Campbell JR, Campbell TJ (1986) Diagnosis and management of Hirschsprung’s disease. A 25 year perspective. AJS 152:49–56CrossRef Harrison MW, Deitz DM, Campbell JR, Campbell TJ (1986) Diagnosis and management of Hirschsprung’s disease. A 25 year perspective. AJS 152:49–56CrossRef
14.
go back to reference Dalkey N, Helmer O (1963) An experimental application of the Delphi method to the use of experts. Manag Sci 9:458–467CrossRef Dalkey N, Helmer O (1963) An experimental application of the Delphi method to the use of experts. Manag Sci 9:458–467CrossRef
16.
go back to reference Brearly S, Armstrong GR, Nairn R et al (1987) Pseudomembranous colitis: a lethal complication of Hirschsprung’s disease unrelated to antibiotic usage. J Pediatr Surg 22:257–259CrossRefPubMed Brearly S, Armstrong GR, Nairn R et al (1987) Pseudomembranous colitis: a lethal complication of Hirschsprung’s disease unrelated to antibiotic usage. J Pediatr Surg 22:257–259CrossRefPubMed
17.
go back to reference Marty TL, Seo T, Matlak ME et al (1995) Gastrointestinal function after surgical correction of Hirschsprung’s disease: long-term follow-up in 135 patients. J Pediatr Surg 30:655–658CrossRefPubMed Marty TL, Seo T, Matlak ME et al (1995) Gastrointestinal function after surgical correction of Hirschsprung’s disease: long-term follow-up in 135 patients. J Pediatr Surg 30:655–658CrossRefPubMed
18.
go back to reference Fujimoto T (1988) Natural history and pathophysiology of enterocolitis in the piebald lethal mouse model of Hirschsprung’s disease. J Pediatr Surg 23:237–242CrossRefPubMed Fujimoto T (1988) Natural history and pathophysiology of enterocolitis in the piebald lethal mouse model of Hirschsprung’s disease. J Pediatr Surg 23:237–242CrossRefPubMed
21.
go back to reference Romeo G, Ronchetto P, Luo Y et al (1994) Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung’s disease. Nature 367:377–378. doi:10.1038/367377a0 CrossRefPubMed Romeo G, Ronchetto P, Luo Y et al (1994) Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung’s disease. Nature 367:377–378. doi:10.​1038/​367377a0 CrossRefPubMed
24.
go back to reference Schuchardt A, D’Agati V, Larsson-Blomberg L et al (1994) Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 367:380–383. doi:10.1038/367380a0 CrossRefPubMed Schuchardt A, D’Agati V, Larsson-Blomberg L et al (1994) Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 367:380–383. doi:10.​1038/​367380a0 CrossRefPubMed
26.
go back to reference Gariepy CE, Cass DT, Yanagisawa M (1996) Null mutation of endothelin receptor type B gene in spotting lethal rats causes aganglionic megacolon and white coat color. Proc Natl Acad Sci USA 93:867–872CrossRefPubMedPubMedCentral Gariepy CE, Cass DT, Yanagisawa M (1996) Null mutation of endothelin receptor type B gene in spotting lethal rats causes aganglionic megacolon and white coat color. Proc Natl Acad Sci USA 93:867–872CrossRefPubMedPubMedCentral
30.
go back to reference Cheng Z, Wang X, Dhall D et al (2010) Splenic lymphopenia in the endothelin receptor B-null mouse: implications for Hirschsprung associated enterocolitis. Pediatr Surg Int 27:145–150. doi:10.1007/s00383-010-2787-y CrossRef Cheng Z, Wang X, Dhall D et al (2010) Splenic lymphopenia in the endothelin receptor B-null mouse: implications for Hirschsprung associated enterocolitis. Pediatr Surg Int 27:145–150. doi:10.​1007/​s00383-010-2787-y CrossRef
38.
39.
go back to reference Berlin C, Berg EL, Briskin MJ et al (1993) Alpha 4 beta 7 integrin mediates lymphocyte binding to the mucosal vascular addressin MAdCAM-1. Cell 74:185–195CrossRefPubMed Berlin C, Berg EL, Briskin MJ et al (1993) Alpha 4 beta 7 integrin mediates lymphocyte binding to the mucosal vascular addressin MAdCAM-1. Cell 74:185–195CrossRefPubMed
41.
go back to reference Bowman EP, Kuklin NA, Youngman KR et al (2002) The intestinal chemokine thymus-expressed chemokine (CCL25) attracts IgA antibody-secreting cells. J Exp Med 195:269–275CrossRefPubMedPubMedCentral Bowman EP, Kuklin NA, Youngman KR et al (2002) The intestinal chemokine thymus-expressed chemokine (CCL25) attracts IgA antibody-secreting cells. J Exp Med 195:269–275CrossRefPubMedPubMedCentral
42.
go back to reference Uren TK, Johansen F-E, Wijburg OLC et al (2003) Role of the polymeric Ig receptor in mucosal B cell homeostasis. J Immunol 170:2531–2539CrossRefPubMed Uren TK, Johansen F-E, Wijburg OLC et al (2003) Role of the polymeric Ig receptor in mucosal B cell homeostasis. J Immunol 170:2531–2539CrossRefPubMed
48.
go back to reference Teitelbaum DH, Caniano DA, Qualman SJ (1989) The pathophysiology of Hirschsprung’s-associated enterocolitis: importance of histologic correlates. J Pediatr Surg 24:1271–1277CrossRefPubMed Teitelbaum DH, Caniano DA, Qualman SJ (1989) The pathophysiology of Hirschsprung’s-associated enterocolitis: importance of histologic correlates. J Pediatr Surg 24:1271–1277CrossRefPubMed
49.
go back to reference Aslam A, Spicer RD, Corfield AP (1997) Biochemical analysis of colonic mucin glycoproteins in children with Hirschsprung disease show disease specific alterations. Biochem Soc Trans 25:8SCrossRefPubMed Aslam A, Spicer RD, Corfield AP (1997) Biochemical analysis of colonic mucin glycoproteins in children with Hirschsprung disease show disease specific alterations. Biochem Soc Trans 25:8SCrossRefPubMed
52.
53.
go back to reference De Filippo C, Pini-Prato A, Mattioli G et al (2010) Genomics approach to the analysis of bacterial communities dynamics in Hirschsprung’s disease-associated enterocolitis: a pilot study. Pediatr Surg Int 26:465–471. doi:10.1007/s00383-010-2586-5 CrossRefPubMed De Filippo C, Pini-Prato A, Mattioli G et al (2010) Genomics approach to the analysis of bacterial communities dynamics in Hirschsprung’s disease-associated enterocolitis: a pilot study. Pediatr Surg Int 26:465–471. doi:10.​1007/​s00383-010-2586-5 CrossRefPubMed
56.
60.
go back to reference El-Sawaf M, Siddiqui S, Mahmoud M et al (2013) Probiotic prophylaxis after pullthrough for Hirschsprung disease to reduce incidence of enterocolitis: a prospective, randomized, double-blind, placebo-controlled, multicenter trial. J Pediatr Surg 48:111–117. doi:10.1016/j.jpedsurg.2012.10.028 CrossRefPubMed El-Sawaf M, Siddiqui S, Mahmoud M et al (2013) Probiotic prophylaxis after pullthrough for Hirschsprung disease to reduce incidence of enterocolitis: a prospective, randomized, double-blind, placebo-controlled, multicenter trial. J Pediatr Surg 48:111–117. doi:10.​1016/​j.​jpedsurg.​2012.​10.​028 CrossRefPubMed
Metadata
Title
Established and emerging concepts in Hirschsprung’s-associated enterocolitis
Author
Ankush Gosain
Publication date
01-04-2016
Publisher
Springer Berlin Heidelberg
Published in
Pediatric Surgery International / Issue 4/2016
Print ISSN: 0179-0358
Electronic ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-016-3862-9

Other articles of this Issue 4/2016

Pediatric Surgery International 4/2016 Go to the issue