A foregut duplication cyst occurring together with both a congenital cystic pulmonary airway malformation and extralobar pulmonary sequestration is an unusual combination. Prenatal ultrasound, MRI, and postnatal CT are helpful for operative planning. Surgical resection is the definitive management for all three anomalies.
Keywords: cystic lung disease; cystic pulmonary airway malformation; esophageal duplication cyst; extralobar pulmonary sequestration; prenatal imaging.
© 2019 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.