Abstract
Congenital cystic adenomatoid malformation (CCAM) recently being referred as congenital pulmonary airway malformation (CPAM), is a rare congenital pulmonary anomaly with reported incidence of 1 in 25,000–35,000 live births.1 On antenatal ultrasonography (USG), characteristic appearance of lesion not only helps in diagnosing it but also excludes other fetal lung anomalies. We present here a case of CCAM.
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