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10.3904/kjim.2016.242

http://scihub22266oqcxt.onion/10.3904/kjim.2016.242
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C5339473!5339473!28264540
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suck abstract from ncbi

pmid28264540      Korean+J+Intern+Med 2017 ; 32 (2): 229-38
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  • Diagnosis and treatment of cystic lung disease #MMPMID28264540
  • Park S; Lee EJ
  • Korean J Intern Med 2017[Mar]; 32 (2): 229-38 PMID28264540show 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.
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