Newborn male presented with congenital diaphragmatic hernia and choledochal cyst: A case report

摘要

Infants with congenital diaphragmatic hernia (CDH) have an increased incidence of associated malformations, ranging from 10% to 50% higher than the general population [1–5]. Choedochal cysts, congenital cystic dilations of the biliary tree, are anomalies that have not yet been described in association with CDH. We describe a patient with a left congenital diaphragmatic hernia who was later diagnosed with a choledochal cyst. Highlights ? Congenital Diaphragmatic hernia in association with a choledochal cyst is a rare finding. ? Both can be successfully treated in light of the other in a stable patient. ? Always be wary of additional congenital anomalies in patients.