Spivey John F, Ramachandran Venkataraman, Graff Gavin R
Department of Child Health, University of Missouri Health Care, Columbia, Missouri, USA.
Pediatr Pulmonol. 2004 Mar;37(3):279-82. doi: 10.1002/ppul.10439.
Congenital diaphragmatic hernias are a relatively common anomaly that can present with significant respiratory morbidity and mortality. We report on a case of an aortic-hiatal gastric hernia that initially presented with repeated episodes of respiratory distress, which was diagnosed as asthma. The diagnosis of a diaphragmatic hernia was made at 18 months of age. In the operating room, it was noted that it was an aortic hiatal hernia, which was surgically repaired. Subsequently, there has been improvement in daily respiratory symptoms.
先天性膈疝是一种相对常见的异常情况，可伴有严重的呼吸疾病和死亡率。我们报告一例主动脉裂孔胃疝病例，该病例最初表现为反复出现的呼吸窘迫发作，被诊断为哮喘。在18个月大时诊断出膈疝。在手术室中，发现这是一例主动脉裂孔疝，并进行了手术修复。随后，日常呼吸症状有所改善。
