What is Congenital Pulmonary Airway Malformation (CPAM)?
Congenital Pulmonary Airway Malformation (CPAM), previously known as congenital cystic adenomatoid malformation (CCAM), is a rare developmental anomaly of the lung in which a portion of the lung is replaced by a non-functioning mass of cystic or solid tissue. This malformation can lead to various respiratory issues and complications in newborns and infants.