RESUMO
This paper reports the case of an infant born with type I esophageal atresia (EA) associated with duodenal atresia (DA). The critical condition of the patient necessitated an exploratory laparotomy, which revealed severe dilatation of the stomach and duodenum. The routine procedure for repairing type I EA is a delayed primary anastomosis after 10 weeks of age because of the long gap between the two esophageal segments. In our case, due to the concomitant DA, the lower pouch was long enough to allow primary neonatal anastomosis. A radiograph taken with a Hegar dilator in the lower segment via the gastrostomy confirmed this suspicion, and the baby underwent a thoracotomy and primary anastomosis between the esophageal pouches. The authors propose the possibility of primary esophageal anastomosis in similar cases.
Assuntos
Anormalidades Múltiplas/classificação , Anormalidades Múltiplas/cirurgia , Anastomose Cirúrgica/métodos , Duodeno/anormalidades , Duodeno/cirurgia , Atresia Esofágica/classificação , Atresia Esofágica/cirurgia , Anormalidades Múltiplas/diagnóstico por imagem , Fatores Etários , Atresia Esofágica/complicações , Atresia Esofágica/diagnóstico por imagem , Evolução Fatal , Dilatação Gástrica/etiologia , Refluxo Gastroesofágico/etiologia , Gastrostomia , Humanos , Recém-Nascido , Masculino , Radiografia , ToracotomiaRESUMO
Gastric volvulus is an uncommon condition more so in the paediatric age group. The cause of gastric volvulus may be idiopathic or secondary to various congenital or acquired conditions. In this short series of three patients, one had volvulus which was due to ligamentous laxity and mobile spleen, second had congenital postero-lateral diaphragmatic defect and the third had hiatus hernia.