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10.1002/rcr2.108 http://scihub22266oqcxt.onion/10.1002/rcr2.108 C4469148!4469148!26090119     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Respirol+Case+Rep 2015 ; 3 (2): 82-4 Nephropedia Template TP {{tp|p=26090119|t=2015. Pleuroparenchymal fibroelastosis: a rare interstitial lung disease |pdf=|usr=}}{{26090119}} gab.com Text Pleuroparenchymal fibroelastosis: a rare interstitial lung disease JO: Respirol Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=26090119 #FOAvip Pleuroparenchymal fibroelastosis (PPFE) is a newly described form of interstitial lung disease that originates in the upper lung zones and typically progresses to involve the entire lung. The disease may be idiopathic but is often associated with other pre- or coexisting conditions. Pneumothorax is a common complication and can occur at presentation or at other times during the course of the disease. Pathologically, interstitial fibrosis takes the form of a dense consolidation with some preservation of alveolar septal outlines and demonstrates a distinctly abrupt interface with residual normal lung. Unrecognized cases of PPFE may be incorrectly diagnosed as sarcoidosis, atypical idiopathic pulmonary fibrosis, or other unclassifiable interstitial pneumonias. Twit Text FOAVip Pleuroparenchymal fibroelastosis: a rare interstitial lung disease ????Respirol Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=26090119 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26090119 #FOAvip English Wikipedia <ref>{{Cite pmid|26090119}}</ref> Pleuroparenchymal fibroelastosis: a rare interstitial lung disease #MMPMID26090119 English JC; Mayo JR; Levy R; Yee J; Leslie KO Respirol Case Rep 2015[Jun]; 3 (2): 82-4 PMID26090119show ga Pleuroparenchymal fibroelastosis (PPFE) is a newly described form of interstitial lung disease that originates in the upper lung zones and typically progresses to involve the entire lung. The disease may be idiopathic but is often associated with other pre- or coexisting conditions. Pneumothorax is a common complication and can occur at presentation or at other times during the course of the disease. Pathologically, interstitial fibrosis takes the form of a dense consolidation with some preservation of alveolar septal outlines and demonstrates a distinctly abrupt interface with residual normal lung. Unrecognized cases of PPFE may be incorrectly diagnosed as sarcoidosis, atypical idiopathic pulmonary fibrosis, or other unclassifiable interstitial pneumonias. äPleuroparenchymal fibroelastosis: a rare interstitial lung disease (epmc).pdf DeepDyve Pubget Overpricing