SOC

Surgery on Children Journal aims to publish issues related to Pediatric Surgery, Pediatric Neurosurgery, Pediatric Plastic Surgery, Pediatric Cardiovascular Surgery, Pediatric Orthopedic Surgery, Pediatric Vascular Surgery, Pediatric Gynecology and Obstetrics, Pediatric Ear Nose Throat, Ophthalmology, Pediatric Anesthesiology and Reanimation, Pediatric Urology, Pediatric Surgical Intensive Care Clinic, and other clinical surgery fields on children of the highest scientific and clinical value at an international level and accepts articles on these topics.

EndNote Style
Index
Case Report
Nutritional and dietary approach in the post-surgical follow-up of hirschsprung disease: a case report
Hirschsprung disease (HD) is a congenital condition caused by abnormal development of the enteric nervous system during the embryonic period, characterized by colonic aganglionosis. Total Colonic Aganglionosis (TCA) refers to the involvement of the entire colon extending to the terminal ileum, accounting for 3–12% of all HD cases. A 45-month-old male patient presented to the clinic with complaints of frequent vomiting and more than 10 watery diarrhea episodes per day. The patient's medical history revealed the development of short bowel syndrome (SBS) following Total Colonic Aganglionosis. Physical examination indicated a poor general condition, decreased skin turgor and tonus, along with growth and developmental delay. Laboratory findings demonstrated low sodium (Na) and potassium (K) levels with electrolyte imbalances. A low-carbohydrate, high-protein diet was planned alongside hydration therapy. Additionally, the family was educated on nutritional management and avoiding harmful foods. Following 17 days of treatment and dietary interventions, the patient's weight increased by 1.5 kg, and complaints of diarrhea and vomiting subsided. During a two-year follow-up period, a reduction in hospitalization frequency and improvements in the patient’s overall clinical condition were observed. The individualized treatment and nutritional plan significantly enhanced the patient’s quality of life. The management of short bowel syndrome, which may develop after HD surgery, requires individualized nutritional plans, a multidisciplinary approach, and continuity in patient-family education, all of which are critically important.


1. Wang D, Zhu T, Zhu L, et al. Screening of undernutrition in children with Hirschsprung disease using preoperative anthropometric parameters: a multicenter cross-sectional study. JPEN. 2023;47(1):151-158. doi:10.1002/jpen.2440
2. Bhargava A, Khedkar K. Chronic constipation unmasking as Hirschsprung disease in a preadolescent: delayed presentation or delayed diagnosis?Cureus. 2024;16(5):e60315. doi:10.7759/cureus.60315
3. Ostertag-Hill CA, Nandivada P, Dickie BH. Late diagnosis of Hirschsprung disease: clinical presentation and long-term functional outcomes.J Pediatr Surg. 2024;59(2):220-224. doi:10.1016/j.jpedsurg. 2023.10.018
4. Koç N, Gündüz M, Ünal Ö, Güney D, Şenaylı A, Şenel E. Nutritional management in a total colonic aganglionosis with ileostomy: case report. Ortadoğu Tıp Derg. 2018;10(2):201-204. doi:10.21601/ortadogutipdergisi.331397
5. Nasr A, Grandpierre V, Sullivan KJ, Wong CA, Benchimol EI. Long-term Outcomes of patients surgically treated for Hirschsprung disease.J Can Assoc Gastroenterol. 2020;4(5):201-206. doi:10.1093/jcag/gwaa026
6. Cesur C, Celayir A. Çocuklarda Hirschsprung hastalığı cerrahi tedavisi sonuçları: 12 yıllık bir deneyim. Turkish Assoc Pediatr Surg. 2021;35(2): 56-64. doi:10.5222/JTAPS.2021.49092
7. Coletta R, Khalil BA, Morabito A. Short bowel syndrome in children: surgical and medical perspectives.Semin Pediatr Surg. 2014;23(5):291-297. doi:10.1053/j.sempedsurg.2014.09.010
8. Andorsky DJ, Lund DP, Lillehei CW, et al. Nutritional and other postoperative management of neonates with short bowel syndrome correlates with clinical outcomes.J Pediatr. 2001;139(1):27-33. doi:10. 1067/mpd.2001.114481
9. Duro D, Kamin D, Duggan C. Overview of pediatric short bowel syndrome.J Pediatr Gastroenterol Nutr. 2008;47(Suppl 1):S33-S36. doi: 10.1097/MPG.0b013e3181819007
10. Koptagel E, Kamarli Altun H. (2021). Kısa bağırsak sendromunda tıbbi beslenme tedavisi ve bağırsak adaptasyonunda besin müdahaleleri. J Anatolia Nursing Health Sci. 2021;24(2):291-297. doi:10.17049/ataunihem.643472
11. Donohoe CL, Reynolds JV. Short bowel syndrome.Surgeon. 2010;8(5): 270-279. doi:10.1016/j.surge.2010.06.004
12. Bıyıklı AE, Bıyıklı ET, Akbulut G. Kısa bağırsak sendromunda beslenme desteği. Beslenme ve Diyet Dergisi. 2013;41(2):156-162.
13. Muto M, Kaji T, Onishi S, Yano K, Yamada W, Ieiri S. An overview of the current management of short-bowel syndrome in pediatric patients.Surg Today. 2022;52(1):12-21. doi:10.1007/s00595-020-02207-z
14. Abad-Sinden A, Sutphen J. Nutritional management of pediatric short bowel syndrome. Practical Gastroenterol. 2003;27(12):28-48.
15. Halaweish I, Srinivas S, Farooqui Z, et al. Duhamel versus swenson pull-through for total colonic aganglionosis: a multi-institutional study.J Pediatr Surg. 2024;59(2):216-219. doi:10.1016/j.jpedsurg.2023.10.017
16. Yeker D. Hirschsprung hastalığı cerrahi tedavisinin tarihsel gelişimi. Turkish J Pediatr Surg. 2018;32(3):116-118. doi:10.5222/JTAPS.2018.116
17. Avci V, Beger B. Hirschsprung disease: Duhamel-Martin experiences. Van Med J. 2018;25(3):355-359. doi:10.5505/vtd.2018.02170
18. Puoti MG, Köglmeier J. Nutritional management of intestinal failure due to short bowel syndrome in children.Nutrients. 2022;15(1):62. doi: 10.3390/nu15010062
19. Belza C, Wales PW. Management of pediatric intestinal failure related to short bowel syndrome.Semin Pediatr Surg. 2022;31(3):151175. doi:10. 1016/j.sempedsurg.2022.151175
Volume 2, Issue 3, 2025
Page : 114-117
_Footer