ISOLATED ILEOCECAL FORM OF AGANGLIONOSIS IN A NEWBORN

G. I. Chepurnoy; Чепурной Г. И.; A. V. Leiga; Лейга А. В.; V. B. Katsupeyev; Кацупеев В. Б.; M. G. Chepurnoy; Чепурной М. Г.; N. A. Mikhanoshina; Миханошина Н. А.; B. G. Rozin; Розин Б. Г.; M. V. Kovalev; Ковалев М. В.

doi:10.18821/1560-9510-2019-23-1-52-53

ISOLATED ILEOCECAL FORM OF AGANGLIONOSIS IN A NEWBORN

Authors: Chepurnoy G.I.¹, Leiga A.V.¹, Katsupeyev V.B.¹, Chepurnoy M.G.¹, Mikhanoshina N.A.¹, Rozin B.G.¹, Kovalev M.V.¹
Affiliations:
1. Rostov State Medical University
Issue: Vol 23, No 1 (2019)
Pages: 52-53
Section: CASE REPORT
Submitted: 05.03.2021
Published: 05.02.2019
URL: https://jps-nmp.ru/jour/article/view/119
DOI: https://doi.org/10.18821/1560-9510-2019-23-1-52-53
ID: 119

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Abstract

There is presented a clinical observation of such rare form of Hirschsprung’s disease in a newborn -as terminal aganglionosis of the ileum and hypo-ganglionosis of the cecum, manifested by acute intestinal obstruction. Resection of the ileocecal angle and leaving the distal colon in the child’s body with good functional results in the long-term postoperative period made it possible to affirm the existence of high isolated segmental forms of Hirshprung’s disease.