Related Experiment Video
Updated: Sep 20, 2026

Protocol and Guidelines for Point-of-Care Lung Ultrasound in Diagnosing Neonatal Pulmonary Diseases Based on International Expert Consensus
Published on: March 6, 2019
Congenital cystic adenomatoid malformation of the lung
1Overland Park Regional Medical Center, Kansas, USA.
Abstract:
The etiology of CCAM of the lung remains unclear. Presentations vary, with clinical outcomes that may be unpredictable. The neonatal nurse should be equipped to detect the sometimes subtle radiologic images these lesions produce and should be able to distinguish CCAM from similar chest masses. Expediting this diagnosis postnatally benefits the neonate by preventing further expansion of the cysts, which can cause a cascade of complications, including air leaks, cardiorespiratory compromise, and PPHN.
Related Concept Videos
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Gross Anatomy of the Lungs
