Mechanism of lung development in the aetiology of adult congenital pulmonary airway malformations.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32732323.
- Also identified by DOI 10.1136/thoraxjnl-2020-214752 and PMC identifier 7569368.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Congenital pulmonary airway malformations (CPAMs) are rare lung abnormalities that result in cyst formation and are associated with respiratory distress in infants and malignant potential in adults. The pathogenesis of CPAMs remains unknown but data suggest disruption of the normal proximo-distal programme of airway branching and differentiation. Here, we demonstrate that adult human CPAM are lined with epithelium that retains SOX-2 and thyroid transcription factor-1 immunohistochemical markers, characteristic of the developing lung. However, RALDH-1, another key marker, is absent. This suggests a more complex aetiology for CPAM than complete focal arrest of lung development and may provide insight to the associated risk of malignancy.
Medical subject headings
- Lung
- Respiratory Mucosa
- Respiratory System Abnormalities