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A Stepwise Diagnostic Approach to Cystic Lung Diseases for Radiologists

Authors
Lee, Kyu-ChongKang, Eun-YoungYong, Hwan SeokKim, CherryLee, Ki YeolHwang, Sung HoOh, Yu-Whan
Issue Date
Sep-2019
Publisher
KOREAN RADIOLOGICAL SOC
Keywords
Lung diseases; Computed tomography; Lymphangioleiomyomatosis; Birt-Hogg-Dube syndrome; Histiocytosis; Langerhans cell
Citation
KOREAN JOURNAL OF RADIOLOGY, v.20, no.9, pp.1368 - 1380
Indexed
SCIE
SCOPUS
KCI
Journal Title
KOREAN JOURNAL OF RADIOLOGY
Volume
20
Number
9
Start Page
1368
End Page
1380
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/63430
DOI
10.3348/kjr.2019.0057
ISSN
1229-6929
Abstract
Lung cysts are commonly seen on computed tomography (CT), and cystic lung diseases show a wide disease spectrum. Thus, correct diagnosis of cystic lung diseases is a challenge for radiologists. As the first diagnostic step, cysts should be distinguished from cavities, bullae, pneumatocele, emphysema, honeycombing, and cystic bronchiectasis. Second, cysts can be categorized as single/localized versus multiple/diffuse. Solitary/localized cysts include incidental cysts and congenital cystic diseases. Multiple/diffuse cysts can be further categorized according to the presence or absence of associated radiologic findings. Multiple/diffuse cysts without associated findings include lymphangioleiomyomatosis and Birt-Hogg-Dube syndrome. Multiple/diffuse cysts may be associated with ground-glass opacity or small nodules. Multiple/diffuse cysts with nodules include Langerhans cell histiocytosis, cystic metastasis, and amyloidosis. Multiple/diffuse cysts with ground-glass opacity include pneumocystis pneumonia, desquamative interstitial pneumonia, and lymphocytic interstitial pneumonia. This stepwise radiologic diagnostic approach can be helpful in reaching a correct diagnosis for various cystic lung diseases.
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