Total collectomy in adult woman with Hirschsprung's Disease: a case report

• Autor(a) principal: Michelini, Bárbara Beatriz
• Data de Publicação: 2022
• Outros Autores: Ferro, Cibele Alexandra, Carvalho, Enzo Prandi de, Cadamuro, Fernanda Magni, Cadamuro, Luana Magni, Criscuolo Filho, Luiz Fernando, Vivi, Maria Clara Ferreira, Oliveira, Marilia Siqueira Procopio de, Miranda, Rafaela Melin, Silva, Tacio Antônio Barros, Rodrigues, Tayanne Fonseca, Vivi, Ayder Anselmo Gomes
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: MedNEXT Journal of Medical and Health Sciences
• Texto Completo: https://mednext.zotarellifilhoscientificworks.com/index.php/mednext/article/view/228
• topic: Hirschsprung's disease; Congenital megacolon; Obstruction

Hirschsprung's disease (HD) is a congenital anomaly of innervation of the lower intestine, limited to the colon, resulting from partial or total obstruction. The main symptom is the inability of a newborn to evacuate within 48 hours after birth, which can cause intestinal obstruction in the neonate and megacolon in children and adults. Therefore, this study reported the case of a 30-year-old female patient with HD affecting the entire colon, where we opted for surgical treatment. In the present study, it was emphasized the medical need to have a better understanding of the clinical picture of HD, as well as its complications and the importance of early diagnosis. In the report presented, it was discussed a late diagnosis of HD and how it affects the patient's life. It presented the improvement in the quality of life that can be obtained by offering an accurate diagnosis and adequate treatment for the patient.