Tip 91a: congenital pulmonary adenomatous malformation (CPAM)

Also called congenital cystic adenomatous malformation (CCAM), it is usually detected antenatally with a peak size at 25/40.

The main risk is hydrops fetalis, with high mortality if present.

Reference: Sfakianaki, A. K., & Copel, J. A. (2012). Congenital cystic lesions of the lung: congenital cystic adenomatoid malformation and bronchopulmonary sequestration. Reviews in obstetrics and gynecology5(2), 85.

First published: 22/04/14

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This entry was posted in Antenatal, Congenital anomalies, Respiratory. Bookmark the permalink.

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