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Congenital Cystic Adenomatoid Malformation (CCAM), also known as Congenital Pulmonary Airway Malformation (CPAM), is a rare congenital lung lesion characterized by abnormal lung tissue with cysts. Here are some key points: Causes Developmental Abnormality: Results from abnormal development of lung tissue during fetal growth. Unknown Cause: The exact cause is unknown and is not linked to genetic or chromosomal abnormalities. Symptoms Prenatal Detection: Often detected during routine prenatal ultrasounds as a cyst or mass in the chest. Postnatal Symptoms: Can include respiratory distress, recurrent infections, and in severe cases, heart failure (fetal hydrops)2. Diagnosis Ultrasound: Typically diagnosed through prenatal ultrasound. Imaging: Postnatal chest X-rays and CT scans confirm the diagnosis and assess the extent of the malformation. Treatment Monitoring: Small lesions may not require treatment and can be monitored. Surgical Intervention: Large lesions or those causing symptoms may require surgical removal after birth. Prenatal Surgery: In severe cases, fetal surgery may be considered to remove the lesion before birth. Prognosis With appropriate treatment, many children with CCAM/CPAM can lead healthy lives. Early detection and management are crucial for a better outcome. #Adenomatoid