Dying for Oxygen: Roles of Hypoxia Inducible Factor 2a and 3a during lung development
Congenital lung lesions comprise a broad spectrum of rare but clinically significant developmental abnormalities, including congenital cystic adenomatoid malformation, bronchopulmonary sequestrations, congenital lobar emphysema, and bronchogenic cysts, which are commonly surgically treated. Although the terms congenital cystic adenomatoid malformation, bronchopulmonary sequestrations, congenital lobar emphysema, and bronchogenic cysts are entrenched in clinical usage and comfortably correspond to rigid pathologic definitions, there is a considerable overlap in the findings. Disregarding the controversy about lesion nomenclature and classification, it is widely accepted that congenital lung lesions result from perturbations in lung and airway embryogenesis. It is generally accepted that both place (level in the tracheobronchial tree) and timing (gestational age) of the embryologic insult correlates with the type of lesion and histopathology that is manifested. The objective of this review is to briefly review normal lung development and to analyze the known molecular mechanisms underlying those diseases.
|Keywords||congenital lung lesions, lung diseases|
|Promotor||D. Tibboel (Dick)|
|Publisher||Erasmus University Rotterdam|
|Sponsor||Erasmus MC Rotterdam, J.E. Jurriaanse Stichting|
Huang, Y. (2012, June 29). Dying for Oxygen: Roles of Hypoxia Inducible Factor 2a and 3a during lung development. Erasmus University Rotterdam. Retrieved from http://hdl.handle.net/1765/32784