Abstract

Congenital cystic adenomatoid malformation (CCAM) of lung is a rare congenital cystic lung lesion.. We report a case of CCAM (Stocker type 1) with a brief review of literature. The patient was diagnosed antenatally with fetal MR. As no other associated anomalies or fetal hydrops were observed, no intrauterine intervention was planned. The baby was born at 36 weeks of gestation with an Apgar score of 8 and O2 saturation was 92%. He had respiratory distress and tachypnea.The diagnosis was confirmed with CT examination. The patient was operated due to respiratory distress and the lesion was totally resected.