Congenital pulmonary airway malformation and duplication cyst

Discussion:

The cystic lesion is consistent with a congenital pulmonary airway malformation.  The hypodense lesion within the stomach is consistent with a duplication cyst.

The histological diagnosis of congenital airway pulmonary malformation (CPAM) was confirmed following left lower lobectomy. The duplication cyst has not been resected.

Case contributed by Dr Jonathan Corness.

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