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Updated: Jan 26, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Diverse histopathological patterns in Fleischner-defined interstitial lung abnormalities: Radiologic-Pathologic
Taiki Fukuda1, Kaori Ishida2, Tomonori Tanaka3
1Center for Pulmonary Functional Imaging, Department of Radiology, Brigham and Women's Hospital and Harvard Medical School, 75 Francis St, Boston, MA, 02115, USA; Department of Radiology, The Jikei University School of Medicine, 3-25-8 Nishi-shinbashi, Minato-ku, Tokyo, 105-8461, Japan.
Interstitial lung abnormalities (ILA) often represent early interstitial lung disease (ILD). This study found most Fleischner-defined ILA cases reclassified as subclinical ILD by 2025 ATS criteria, revealing diverse histopathology beyond usual interstitial pneumonia (UIP).
Area of Science:
- Pulmonary Medicine
- Radiology
- Pathology
Background:
- Interstitial lung abnormalities (ILA) are CT-detected findings that may indicate early interstitial lung disease (ILD).
- Histopathologic data correlating with ILA and ILD are limited, with prior studies yielding conflicting results.
- The 2025 American Thoracic Society (ATS) criteria aim to differentiate ILA from ILD.
Purpose of the Study:
- To examine the histopathological spectrum of Fleischner Society-defined ILA.
- To correlate histopathological findings with CT features and patient outcomes.
- To reclassify ILA cases based on the 2025 ATS criteria.
Main Methods:
- Retrospective analysis of 30 patients with surgical lung biopsies for ILA (2010-2021).
- Histopathological evaluation by three pulmonary pathologists and CT assessment by two radiologists.
- Comparison of overall survival between usual interstitial pneumonia (UIP)-related and non-UIP-related groups.
Main Results:
- Most patients (90%) had fibrotic ILA, predominantly reclassified as subclinical ILD (96.7%) per 2025 ATS criteria.
- Usual interstitial pneumonia (UIP) was the most common dominant pattern (43.3%), followed by nonspecific interstitial pneumonia (NSIP) and bronchiolocentric interstitial pneumonia (BIP) (20% each).
- CT findings included reticular opacity and traction bronchiectasis for UIP/NSIP, and branching linear opacities for BIP. No significant difference in overall survival was observed between UIP-related and non-UIP-related groups.
Conclusions:
- Fleischner-defined ILA, when reclassified by 2025 ATS criteria, is frequently subclinical ILD.
- The histopathology of ILA is heterogeneous, extending beyond UIP to include patterns like BIP.
- These findings underscore the importance of histopathological diversity in understanding ILA and its progression to ILD.
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