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PMID: 16860157 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Review

Pathology of bronchopulmonary dysplasia.

Seminars in perinatology ·Vol. 30 ·No. 4 ·2006-08-00 ·Pages 179-84

Coalson JJ

Abstract

Over the past three decades, advances in prenatal and neonatal intensive care have contributed to marked improvements in survival rates for extremely immature infants born during the canalicular phase of lung development at 24 to 26 weeks, a time when alveolar and distal vascular development is rapidly occurring. The histopathological lesions of severe airway injury and alternating sites of overinflation and fibrosis in "old" BPD have been replaced in "new" BPD with the pathologic changes of large, simplified alveolar structures, a dysmorphic capillary configuration, and variable interstitial cellularity and/or fibroproliferation. Airway and vascular lesions, when present, tend to be present in infants, who over time develop more severe disease. The concept that "new" BPD results in an arrest in alveolization should be modified to that of an impairment in alveolization as evidence shows that short ventilatory times and/or the use of nCPAP allow continued alveolar formation.

MeSH Terms
Animals Bronchopulmonary Dysplasia/pathology Continuous Positive Airway Pressure Disease Models, Animal Humans Infant, Newborn Lung/blood supply,growth & development,pathology Pulmonary Alveoli/embryology
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Coalson Jacqueline J
University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA. [email protected]
Article Info
Journal
Seminars in perinatology
Abbr.
Semin Perinatol
ISSN
0146-0005
Published
2006-08-00
Pages
179-84
Language
English
Region
United States
NLM ID
7801132
Subset
IM
Grants
NHLBI NIH HHS · HL52636 · United States
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