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Unexpected gap between intraoperative caliber change of the intestine and normoganglia in patients with intestinal aganglionosis

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Abstract

Purpose

Intestinal aganglionosis (IA) is so rare that the entity remains unclear. The aim of the present study was to compare the outcomes of patients with IA and those with total colonic aganglionosis (TCA).

Methods

The hospital records were retrospectively reviewed from 1977 to 2018. Outcomes were analyzed for the IA group and the TCA group, including clinical presentation, initial management, and operative details.

Results

There were six patients were managed in IA (all male) and seven patients in TCA (4 male). The median age at the first operation was significantly younger in IA than TCA (2 days vs 24 days, p = 0.01). The gap between the intraoperative caliber change (CC) of the intestine and the initial stoma location was not significantly different (7.5 cm vs 12 cm, p = 0.61), but the rate of stoma dysfunction was significantly higher in IA (83% vs 0%, p = 0.005). The gap between the CC and the ganglionated bowel was significantly longer in IA (85 cm vs 10 cm, p = 0.003).

Conclusion

Patients with IA appear to have a high risk for stoma dysfunction after the first operation because of the unexpected gap between the CC and normoganglia. The initial location of the stoma requires careful consideration.

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References

  1. Moore SW (2015) Total colonic aganglionosis and Hirschsprung’s disease: a review. Pediatr Surg Int 31:1–9. https://doi.org/10.1007/s00383-014-3634-3

    Article  CAS  PubMed  Google Scholar 

  2. Taguchi T, Obata S, Ieiri S (2017) Current status of Hirschsprung’s disease: based on a nationwide survey of Japan. Pediatr Surg Int 33:497–504. https://doi.org/10.1007/s00383-016-4054-3

    Article  PubMed  Google Scholar 

  3. Hukkinen M, Koivusalo A, Merras-Salmio L et al (2015) Postoperative outcome and survival in relation to small intestinal involvement of total colonic aganglionosis. J Pediatr Surg 50:1859–1864. https://doi.org/10.1016/j.jpedsurg.2015.05.017

    Article  PubMed  Google Scholar 

  4. Hidouri S, Zitouni H, Chahed J et al (2017) Familial near-total intestinal aganglionosis. J Neonatal Surg 6:62. https://doi.org/10.2169/jns.v6i3.562

    Article  Google Scholar 

  5. Sarin YK, Raj P, Thakkar N (2014) Perils of total colonic aganglionosis presenting in neonatal age. J Neonatal Surg 3:28

    Google Scholar 

  6. Moore SW, Zaahl M (2009) Clinical and genetic differences in total colonic aganglionosis in Hirschsprung’s disease. J Pediatr Surg 44:1899–1903. https://doi.org/10.1016/j.jpedsurg.2009.04.026

    Article  PubMed  Google Scholar 

  7. Nakamura H, Henderson D, Puri P (2017) A meta-analysis of clinical outcome of intestinal transplantation in patients with total intestinal aganglionosis. Pediatr Surg Int 33:837–841. https://doi.org/10.1007/s00383-017-4107-2

    Article  PubMed  Google Scholar 

  8. Zani A, Eaton S, Morini F et al (2017) European paediatric surgeons’ association survey on the management of hirschsprung disease. Eur J Pediatr Surg 27:096–101. https://doi.org/10.1055/s-0036-1593991

    Article  Google Scholar 

  9. Ziegler MM, Royal RE, Brandt J et al (1993) Extended myectomy-myotomy. A therapeutic alternative for total intestinal aganglionosis. Ann Surg 218:504–511. https://doi.org/10.1097/00000658-199310000-00010

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Shimotake T, Tomiyama H, Aoi S, Iwai N (2003) Discrepancy between macroscopic and microscopic transitional zones in Hirschsprung's disease with reference to the type of RET/GDNF/SOX10 gene mutation. J Pediatr Surg 38:698–701. https://doi.org/10.1016/jpsu.2003.50186

    Article  PubMed  Google Scholar 

  11. Ruttenstock E, Puri P (2009) A meta-analysis of clinical outcome in patients with total intestinal aganglionosis. Pediatr Surg Int 25:833–839. https://doi.org/10.1007/s00383-009-2439-2

    Article  PubMed  Google Scholar 

  12. Frischer JS, Azizkhan RG (2012) Jejunoileal atresia and stenosis. In: Coran AG (ed) Pediatric surgery, 7th edn. Elsevier, Oxford, pp 1059–1071

    Chapter  Google Scholar 

  13. Badner JA, Siebert WK, Garver KL, Chakravarti A (1990) A genetic study of Hirschsprung disease. Am J Hum Genet 46:568–580

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Sathe M, Houwen R (2017) Meconium ileus in cystic fibrosis. J Cyst Fibros 16:S32–S39. https://doi.org/10.1016/j.jcf.2017.06.007

    Article  PubMed  Google Scholar 

  15. White FV, Langer JC (2000) Circumferential distribution of ganglion cells in the transition zone of children with Hirschsprung disease. Pediatr Dev Pathol 3:216–222

    Article  CAS  PubMed  Google Scholar 

  16. Kapur RP, Kennedy AJ (2013) Histopathologic delineation of the transition zone in short-segment Hirschsprung disease. Pediatr Dev Pathol 16:252–266. https://doi.org/10.2350/12-12-1282-oa.1

    Article  PubMed  Google Scholar 

  17. Kapur RP (2016) Histology of the transition zone in Hirschsprung disease. Am J Surg Pathol 40:1637–1646. https://doi.org/10.1097/PAS.0000000000000711

    Article  PubMed  Google Scholar 

  18. Rabah R (2010) Total colonic aganglionosis case report, practical diagnostic approach and pitfalls. Arch Pathol Lab Med 134:1467–1473. https://doi.org/10.1043/2010-0279-CR.1

    Article  PubMed  Google Scholar 

  19. Maia DM (2000) The reliability of frozen-section diagnosis in the pathologic evaluation of Hirschsprung’s disease. Am J Surg Pathol 24:1675–1677. https://doi.org/10.1097/00000478-200012000-00013

    Article  CAS  PubMed  Google Scholar 

  20. Kapur RP, Kennedy AJ (2012) Transitional zone pull through: surgical pathology considerations. Semin Pediatr Surg 21:291–301. https://doi.org/10.1053/j.sempedsurg.2012.07.003

    Article  PubMed  Google Scholar 

  21. Friedmacher F, Puri P (2013) Classification and diagnostic criteria of variants of Hirschsprung’s disease. Pediatr Surg Int 29:855–872. https://doi.org/10.1007/s00383-013-3351-3

    Article  PubMed  Google Scholar 

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Correspondence to Akinori Sekioka.

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Akinori Sekioka, Koji Fukumoto, Hiromu Miyake, Kengo Nakaya, Akiyoshi Nomura, Yutaka Yamada, Susumu Yamada, and Naoto Urushihara have no conflicts of interest or financial ties to disclose.

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Sekioka, A., Fukumoto, K., Miyake, H. et al. Unexpected gap between intraoperative caliber change of the intestine and normoganglia in patients with intestinal aganglionosis. Pediatr Surg Int 35, 1115–1121 (2019). https://doi.org/10.1007/s00383-019-04534-w

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