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Updated: May 14, 2026

Refined Murine Model of Idiopathic Pulmonary Fibrosis
Published on: June 17, 2025
Combined pulmonary fibrosis and emphysema
Spyros A Papiris1, Christina Triantafillidou, Effrosyni D Manali
1Second Pulmonary Medicine Department, Attikon University Hospital, Athens Medical School, National and Kapodistrian University of Athens, Greece. papiris@otenet.gr
Computed tomography enables identification of combined pulmonary fibrosis and emphysema (CPFE). This condition, common in male smokers, presents unique physiological traits and potential complications.
Area of Science:
- Pulmonology
- Radiology
- Pathology
Background:
- Computed tomography (CT) allows for the recognition of combined pulmonary fibrosis and emphysema (CPFE).
- CPFE typically presents with emphysema in upper lobes and fibrosis in lower lobes.
- Patients are predominantly male smokers with preserved lung volumes and reduced diffusion capacity.
Purpose of the Study:
- To define and characterize combined pulmonary fibrosis and emphysema (CPFE).
- To outline the diagnostic criteria for CPFE using imaging and pathological findings.
- To discuss the complications and distinct outcomes associated with CPFE.
Main Methods:
- Utilizing computed tomography (CT) for radiological assessment of emphysema and interstitial pneumonia patterns.
- Pathological confirmation of idiopathic usual interstitial pneumonia (IP).
- Review of patient demographics, smoking history, and physiological profiles.
Main Results:
- CPFE is defined by the coexistence of radiological emphysema and either CT-IP pattern or pathologically confirmed IP.
- Emphysema predominantly affects upper lobes, while fibrosis is observed in lower lobes.
- Patients exhibit preserved lung volumes and significantly reduced diffusion capacity.
Conclusions:
- CPFE is a distinct clinical entity identifiable through advanced imaging techniques.
- CPFE is associated with complications such as pulmonary hypertension, lung cancer, and acute lung injury.
- The clinical course and outcomes of CPFE may differ from those of isolated pulmonary fibrosis or emphysema.
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