EXPERIENCE IN IMPROVING SURGICAL TREATMENT WHEN IMPOSING A STOMA IN CHILDREN WITH HIRSPRUNG'S DISEASE

Abstract

Hirpsprung's disease most often manifests as symptoms of intestinal obstruction, characterized by the colon nervous system congenital disability, frequent bloating, and impaired stool passage up to the clinic of intestinal obstruction. In recent years, this pathology has belonged to the group of neuro-crystopathy. The leading cause of death is the development of severe enterocolitis. Due to the lack of clear clinical manifestations, it is often observed that this disease goes undetected during the neonatal period. Currently, the only treatment is surgery. The final diagnosis is made after examining  histopathological specimens, the diagnosis of which is difficult due to incomplete differentiation of the mucous and intermuscular layers in infancy.