Korean Guidelines for Diagnosis and Management of Interstitial Lung Disease: Cryptogenic Organizing Pneumonia

Cryptogenic organizing pneumonia (COP), one of the idiopathic interstitial pneumonias (IIP), exhibits an acute or subacute course. It can be diagnosed after excluding secondary causes or diseases. COP accounts for approximately 5% to 10% of IIPs, with the average age of diagnosis ranging from 50 to 60 years. Patients primarily present with dry cough and dyspnea. They often experience fever, fatigue, and weight loss. Common radiologic findings on high-resolution computed tomography include localized consolidations, which are typically subpleural or located in the lower zones, though they can occur in all regions of the lungs. While treatment can be initiated without histopathological diagnosis, tissue biopsy may be necessary when the diagnosis is unclear. Response to steroid therapy is generally good, with rapid clinical improvement and a favorable prognosis, although relapses are common.

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Publication Details

Journal
Tuberculosis & respiratory diseases
Published
2025-03-13
DOI
https://doi.org/10.4046/trd.2024.0167
Citations
1
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
1.52
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article

Korean Guidelines for Diagnosis and Management of Interstitial Lung Disease: Cryptogenic Organizing Pneumonia

Sun Hyo Park, H. Jang, Yong Suk Jo, Joon-Sung Joh et al.
1 citations
Tuberculosis & respiratory diseases
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
1.52
article

Korean Guidelines for Diagnosis and Management of Interstitial Lung Disease: Cryptogenic Organizing Pneumonia

Sun Hyo Park, H. Jang, Yong Suk Jo, Joon-Sung Joh, Jong Sun Park, Hyun-Kyung Lee
article en
1 citations

Abstract

Cryptogenic organizing pneumonia (COP), one of the idiopathic interstitial pneumonias (IIP), exhibits an acute or subacute course. It can be diagnosed after excluding secondary causes or diseases. COP accounts for approximately 5% to 10% of IIPs, with the average age of diagnosis ranging from 50 to 60 years. Patients primarily present with dry cough and dyspnea. They often experience fever, fatigue, and weight loss. Common radiologic findings on high-resolution computed tomography include localized consolidations, which are typically subpleural or located in the lower zones, though they can occur in all regions of the lungs. While treatment can be initiated without histopathological diagnosis, tissue biopsy may be necessary when the diagnosis is unclear. Response to steroid therapy is generally good, with rapid clinical improvement and a favorable prognosis, although relapses are common.

Tuberculosis & respiratory diseasesVol. 88(3)
Seoul National University Bundang Hospital (KR), Inje University Busan Paik Hospital (KR), National Medical Center (KR), Inha University Hospital (KR), The Catholic University of Korea Seoul St. Mary's Hospital (KR), Keimyung University (KR), Catholic University of Korea (KR)
Good health and well-being
Openalex Percentile: Top 21%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
1.52
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Korean Guidelines for Diagnosis and Management of Interstitial Lung Disease: Cryptogenic Organizing Pneumonia — Sun Hyo Park, H. Jang, et al. · Tuberculosis & respiratory diseases (2025) | TGRS Research Map | TGRS