Corneillie P, Gruwez J A, Lerut T
Acta Chir Belg. 1985 Jan-Feb;85(1):17-24.
The authors report two cases of congenital abnormal rightsided high insertion of the diaphragm. Though there was no acute respiratory distress in the neonatal period, both presented other congenital deformities that required further investigation. At one month of age, both children developed severe respiratory problems, leading to a semi-urgent surgical intervention, that revealed the final diagnosis of high insertion. The discussion, following the embryological development, underlines the rarity of this anomaly.
作者报告了两例先天性右侧膈肌高位插入异常的病例。尽管在新生儿期没有急性呼吸窘迫，但两人都存在其他需要进一步检查的先天性畸形。在1个月大时，两个孩子都出现了严重的呼吸问题，导致了半紧急的手术干预，最终确诊为高位插入。根据胚胎发育进行的讨论强调了这种异常的罕见性。
