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- W2114289069 abstract "Diffuse cystic and nodular lung diseases have characteristic imaging findings. The most common causes of cystic lung disease are lymphangioleiomyomatosis and Langerhans cell histiocytosis. Other less common cystic lung diseases include Birt-Hogg-Dube syndrome, lymphocytic interstitial pneumonitis, and light chain deposition disease. Computed tomography is used to differentiate cystic lung disease from emphysema, honeycombing, cavities, and bronchiectasis, which mimic cystic lung disease. Diffuse nodular lung disease are categorized as centrilobular, perilymphatic, and random types. In diffuse nodular lung disease, a specific diagnosis is achieved through a combination of history, physical examination, and imaging findings." @default.
- W2114289069 created "2016-06-24" @default.
- W2114289069 creator A5019650350 @default.
- W2114289069 creator A5023897162 @default.
- W2114289069 creator A5076102496 @default.
- W2114289069 date "2015-06-01" @default.
- W2114289069 modified "2023-10-18" @default.
- W2114289069 title "Cystic and Nodular Lung Disease" @default.
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- W2114289069 doi "https://doi.org/10.1016/j.ccm.2015.02.011" @default.
- W2114289069 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26024606" @default.
- W2114289069 hasPublicationYear "2015" @default.
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