Hirschsprung’s disease: epidemiology, diagnosis, and treatment in a retrospective hospital-based study

https://doi.org/10.19106/JMedSci005302202103

Andi Sinapati Palissei(1), Ahmadwirawan Ahmadwirawan(2), Muhammad Faruk(3*)

(1) Department of Surgery, Faculty of Medicine, Hasanuddin University, Makassar
(2) Division of Pediatric Surgery, Department of Surgery, Faculty of Medicine, Hasanuddin University, Makassar
(3) Department of Surgery, Faculty of Medicine, Hasanuddin University, Makassar
(*) Corresponding Author

Abstract


Hirschsprung’s disease (HD), or congenital megacolon, is a disease characterized
by the absence of ganglion cells in the myenteric (Auerbach’s) and submucosal
(Meissner’s) plexuses of the intestine, causing maximum obstruction in
neonates. The purpose of this study was to investigate patient characteristics,
clinical presentation, investigations, surgical treatment, and outcome. This
study is a retrospective study of HD cases. Data obtained from medical records
at the institution. Of the 109 with a positive rectal biopsy diagnosis, 91 were
patients with this disease. There were more cases in boys than girls with a
ratio of 1.37: 1. The patients were grouped into 4 age groups: neonates 29 cases
(26.61%); infants/toddlers/young children 55 cases (50.46%); children over 5
years16 cases (14.69%); and teenagers 9 cases (8.24%). The neonates generally
presented with abdominal distension, green vomiting, and a history of delayed
meconium release, while the toddler, child, and adolescent groups experienced
constipation and abdominal distension. Furthermore, from 37 patients (33.94%)
that got barium enema examination, the most common transition zone was
observed in the rectosigmoid (17 patients, or 45.9%). In addition, The Duhamel
procedure was the most frequent pull-through procedure found in our cohort
which was performed in 40 patients (36.70%). In conclusion, HD is mostly found
in male infants/toddlers/young children with abdominal distention and chronic
constipation as common symptoms. The barium enema shows the rectosigmoid
as the most common transition zone, while the Duhamel pull-through procedure
is the primary definitive operative action performed.

Keywords


Chronic Constipation; Pull-through; Hirschsprung;

Full Text:

PDF


References

  1. Gunadi, Karina SM, Dwihantoro A. Outcomes in patients with hirschsprung disease following definitive surgery. BMC Res Notes 2018;11(1):1-5. https://doi.org/10.1186/s13104-018-3751-5
  2. Grosfeld IL. Hirschsprung's disease: a historical perspective - 1691-2005. In: hirschsprung's disease and allied disorders. Berlin, Heidelberg: Springer Berlin Heidelberg. 2008: 1-12. https://doi.org/10.1007/978-3-540-33935-9_1
  3. Gosain A. Established and emerging concepts in Hirschsprung's-associated enterocolitis. Pediatr Surg Int 2016;32(4):313-20. https://doi.org/10.1007/s00383-016-3862-9
  4. Alehossein M, Roohi A, Pourgholami M, Mollaeian M, Salamati P. Diagnostic accuracy of radiologic scoring system for evaluation of suspicious hirschsprung disease in children. Iran J Radiol a Q J Publ by Iran Radiol Soc 2015;12(2):e12451. https://doi.org/10.5812/iranjradiol.12451
  5. Mabula JB, Kayange NM, Manyama M, Chandika AB, Rambau PF, Chalya PL. Hirschsprung's disease in children: a five year experience at a university teaching hospital in northwestern Tanzania. BMC Res Notes 2014;7:410. https://doi.org/10.1186/1756-0500-7-410
  6. Szylberg L, Marszałek A. Diagnosis of Hirschsprung's disease with particular emphasis on histopathology. A systematic review of current literature. Prz Gastroenterol 2014;9(5):264-9. https://doi.org/10.5114/pg.2014.46160
  7. Teitelbaum DH, Coran AG. Primary pull-through for Hirschsprung's disease. Semin Neonatol 2003; 8(3):233-41. https://doi.org/10.1016/S1084-2756(03)00026-5
  8. El-Sawaf M, Siddiqui S, Mahmoud M, Drongowski R, Teitelbaum DH. Probiotic prophylaxis after pullthrough for Hirschsprung disease to reduce incidence of enterocolitis: A prospective, randomized, double-blind, placebo-controlled, multicenter trial. J Pediatr Surg 2013; 48(1):111-7. https://doi.org/10.1016/j.jpedsurg.2012.10.028
  9. Cheng LS, Schwartz DM, Hotta R, Graham HK, Goldstein AM. Bowel dysfunction following pullthrough surgery is associated with an overabundance of nitrergic neurons in Hirschsprung disease. J Pediatr Surg 2016; 51(11):1834-8. https://doi.org/10.1016/j.jpedsurg.2016.08.001
  10. Langer JC. Hirschsprung disease. In: Coran AGBT-PS (Seventh E, editor. Philadelphia: Mosby. 2012: 1265-78. https://doi.org/10.1016/B978-0-323-07255-7.00101-X
  11. Mariana N, Asadul Isl A, Hatta M, Fransiscus H. IL23 mRNA Expression in Hirschsprung-Associated Enterocolitis. J Med Sci 2020;20(2):39-43. https://doi.org/10.3923/jms.2020.39.43
  12. Kelleher J, Blake N. Diagnosis of hirschsprung's disease and allied disorders. In: hirschsprung's disease and allied disorders. Berlin, Heidelberg: Springer Berlin Heidelberg. 2008: 145-51.
  13. Arts E, Botden SMBI, Lacher M, Sloots P, Stanton MP, Sugarman I, et al. Duhamel versus transanal endorectal pull through (TERPT) for the surgical treatment of Hirschsprung's disease. Tech Coloproctol 2016; 20(10):677-82. https://doi.org/10.1007/s10151-016-1524-5
  14. Habibie YA. The 3rd Aceh surgery update 2019 in conjugation with the 1st Indonesian General Surgeon Society (PABI) Aceh chapter meeting and the 1st Ikatan Alumni Bedah Unsyiah (IABU) meeting. Bali Med J 2019; 8(3):1. https://doi.org/10.15562/bmj.v8i3.1683
  15. Puri P, Montedonico S. Hirschsprung's disease: clinical features. In: hirschsprung's disease and allied disorders. Berlin, Heidelberg: Springer Berlin Heidelberg. 2008: 107-13. https://doi.org/10.1007/978-3-540-33935-9_8
  16. Austin KM. The pathogenesis of Hirschsprung's disease-associated enterocolitis. Semin Pediatr Surg 2012; 21(4):319-27. https://doi.org/10.1053/j.sempedsurg.2012.07.006
  17. O'Donovan AN, Habra G, Somers S, Malone DE, Rees A, Winthrop AL. Diagnosis of Hirschsprung's disease. AJR Am J Roentgenol 1996; 167(2):517-20. https://doi.org/10.2214/ajr.167.2.8686640
  18. Meier-Ruge W, Bruder E. Histopathological diagnosis and differential diagnosis of hirschsprung's disease. In: hirschsprung's disease and allied disorders. Berlin, Heidelberg: Springer Berlin Heidelberg. 2008: 185-97. https://doi.org/10.1007/978-3-540-33935-9_13
  19. Peyvasteh M, Askarpour S, Ostadian N, Moghimi M-R, Javaherizadeh H. Diagnostic accuracy of barium enema findings in hirschsprung's disease. Arq Bras Cir Dig ABCD = Brazilian Arch Dig Surg 2016;29(3):155-8. https://doi.org/10.1590/0102-6720201600030007
  20. Visser R, van de Ven TJ, van Rooij IALM, Wijnen RMH, de Blaauw I. Is the Rehbein procedure obsolete in the treatment of Hirschsprung's disease? Pediatr Surg Int 2010; 26(11):1117-20. https://doi.org/10.1007/s00383-010-2696-0
  21. Zhang J, Ma T, Peng Y, Huang G, Liu F. A 5-year follow-up study of neonates with Hirschsprung's disease undergoing transanal Soave or Swenson surgery. Patient Prefer Adherence 2017;11:1957-61. https://doi.org/10.2147/PPA.S149722



DOI: https://doi.org/10.19106/JMedSci005302202103

Article Metrics

Abstract views : 5443 | views : 21569




Copyright (c) 2021 Andi Sinapati Palissei, Ahmadwirawan Ahmadwirawan, Muhammad Faruk

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.