What is it about?
Congenital cystic adenomatoid malformation (CCAM) – recently reported as congenital pulmonary airway malformation – is a rare abnormality of lung development. We present a case of a six-year-old child having a cystic lung lesion that proved to be CCAM after surgical resection. The child is performing well on follow-up.
Featured Image
Why is it important?
it helps in clinical differentiation of cases presented with acute respiratory distress
Perspectives
Read the Original
This page is a summary of: It is not pneumothorax: Multicystic lung lesion in a six-year-old child, Proceedings of Singapore Healthcare, August 2016, SAGE Publications,
DOI: 10.1177/2010105816664357.
You can read the full text:
Contributors
The following have contributed to this page