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10.3904/kjim.2016.242 http://scihub22266oqcxt.onion/10.3904/kjim.2016.242 C5339473!5339473 !28264540     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28264540 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\28264540 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Korean+J+Intern+Med 2017 ; 32 (2 ): 229-238 Nephropedia Template TP {{tp|p=28264540 |t=2017. Diagnosis and treatment of cystic lung disease |pdf=|usr=}}{{28264540 }} gab.com Text Diagnosis and treatment of cystic lung disease JO: Korean J Intern Med http://www.kidney.de/pget.php?&tw=1&pmid=28264540 #FOAvip Cystic lung disease (CLD) is a group of lung disorders characterized by the presence of multiple cysts, defined as air-filled lucencies or low-attenuating areas, bordered by a thin wall (usually < 2 mm). The recognition of CLDs has increased with the widespread use of computed tomography. This article addresses the mechanisms of cyst formation and the diagnostic approaches to CLDs. A number of assessment methods that can be used to confirm CLDs are discussed, including high-resolution computed tomography, pathologic approaches, and genetic/ serologic markers, together with treatment modalities, including new therapeutic drugs currently being evaluated. The CLDs covered by this review are lymphangioleiomyomatosis, pulmonary Langerhans cell histiocytosis, Birt-Hogg-Dube syndrome, lymphocytic interstitial pneumonia/follicular bronchiolitis, and amyloidosis. Twit Text FOAVip Diagnosis and treatment of cystic lung disease ????Korean J Intern Med http://www.kidney.de/pget.php?&tw=1&pmid=28264540 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28264540 #FOAvip English Wikipedia <ref>{{Cite pmid|28264540 }}</ref> Diagnosis and treatment of cystic lung disease #MMPMID28264540 Park S ; Lee EJ Korean J Intern Med 2017[Mar]; 32 (2 ): 229-238 PMID28264540 show ga Cystic lung disease (CLD) is a group of lung disorders characterized by the presence of multiple cysts, defined as air-filled lucencies or low-attenuating areas, bordered by a thin wall (usually < 2 mm). The recognition of CLDs has increased with the widespread use of computed tomography. This article addresses the mechanisms of cyst formation and the diagnostic approaches to CLDs. A number of assessment methods that can be used to confirm CLDs are discussed, including high-resolution computed tomography, pathologic approaches, and genetic/ serologic markers, together with treatment modalities, including new therapeutic drugs currently being evaluated. The CLDs covered by this review are lymphangioleiomyomatosis, pulmonary Langerhans cell histiocytosis, Birt-Hogg-Dube syndrome, lymphocytic interstitial pneumonia/follicular bronchiolitis, and amyloidosis. |Amyloidosis/diagnosis [MESH] |Birt-Hogg-Dube Syndrome/diagnosis [MESH] |Cysts/diagnosis/etiology/therapy [MESH] |Histiocytosis, Langerhans-Cell/diagnosis [MESH] |Humans [MESH] |Lung Diseases, Interstitial/diagnosis [MESH] |Lung Diseases/*diagnosis/etiology/*therapy [MESH] |Lung Neoplasms/diagnosis [MESH]Diagnosis and treatment of cystic lung disease (epmc).pdf DeepDyve Pubget Overpricing