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Airspace Enlargement with Fibrosis in a Young Heavy Smoker Mimicking Diffuse Cystic Lung Diseaseopen access

Authors
Bae, K.An, H.J.Jeon, K.N.
Issue Date
Nov-2022
Publisher
MDPI
Keywords
airspace enlargement with fibrosis; computed tomography; emphysema; lung cysts; lymphangioleiomyomatosis; pulmonary Langerhans cell histiocytosis; smoking
Citation
Medicina (Kaunas, Lithuania), v.58, no.11
Indexed
SCIE
SCOPUS
Journal Title
Medicina (Kaunas, Lithuania)
Volume
58
Number
11
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/29799
DOI
10.3390/medicina58111648
ISSN
1010-660X
1648-9144
Abstract
The widespread use of computed tomography (CT) has led to the increased recognition of cystic lung lesions. Multiple pulmonary cysts can be observed in heterogeneous disorders called diffuse cystic lung diseases (DCLDs), which include pulmonary Langerhans cell histiocytosis, lymphangioleiomyomatosis, lymphocytic interstitial pneumonia, and Birt-Hogg-Dubé syndrome. Recently, airspace enlargement with fibrosis (AEF) has been recognized as an entity on the spectrum of smoking-related lung diseases. We report a young male heavy smoker presenting diffuse pulmonary cysts on chest CT with suspected DCLD. However, histopathological examination of the surgical biopsy specimen revealed dilated emphysematous cysts with prominent mural fibrosis, consistent with AEF.
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