Congenital paraesophageal hernia with gastric outlet obstruction in a neonate with Cornelia de Lange Syndrome
Radiology Case Reports(2022)
摘要
We describe a case of a newborn being treated for encephalopathy and seizures, whose radiographs since the first day of life demonstrate a persistent ovoid lucency over the central lower chest. A CT performed confirmed a type IV hiatal hernia, which is defined as a paraesophageal type hernia containing a portion of the abdominal viscera. This infant's hernia included the distal stomach, pylorus, and proximal duodenum. There was no volvulus or ischemic change at surgery. The patient underwent successful reduction, fundoplication, and gastrostomy placement with hospital discharge after further stabilization of additional medical problems. Genetic testing later confirmed Cornelia de Lange Syndrome Type V, which has been associated with gastrointestinal manifestations and congenital diaphragmatic hernias.
更多查看译文
关键词
Congenital paraesophageal hernia,Cornelia de Lange syndrome,Neonatal gastric outlet obstruction,Congenital diaphragmatic hernia,Gastric hernia without volvulus,Type IV hiatal hernia
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要