An adolescent with idiopathic pleuroparenchymal fibroelastosis. Case report
Date
2018Author
KIYAN, GÜRSU
Yilmazbayhan, Dilek
GÖKDEMİR, YASEMİN
ERDEM ERALP, ELA
Karadag, Bulent
Atag, Emine
Ikizoglu, Nilay Bas
Metadata
Show full item recordAbstract
Idiopathic pleuroparenchymal fibroelastosis (IPPFE) is a rare disorder recently included in rare idiopathic interstitial pneumonias according to the updated American Thoracic Society/European Respiratory Society classification. IPPFE is characterized by pleural and subpleural parenchymal fibrosis causing volume loss predominantly in the upper lung lobes. Age of onset is variable, IPPFE mainly occurs in third and fourth decades.
Collections
- Makale [92796]