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02-04-2024 | Interstitial Lung Disease and Pulmonary Fibrosis | REVIEW

Interstitial Lung Abnormalities (ILA) and Pulmonary Fibrosis

Authors: Noriaki Wada, Kyung Soo Lee, Hiroto Hatabu

Published in: Current Pulmonology Reports

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Abstract

Purpose of Review

This review identifies the similarities and differences between interstitial lung abnormalities (ILA) and pulmonary fibrosis in terms of clinical relevance, radiological features, histological features, genetics, pathophysiology, and biomarkers, and presents clinical management with a focus on ILA and future perspectives.

Recent Findings

ILA and pulmonary fibrosis, especially idiopathic pulmonary fibrosis, may share common biological, radiological, and histopathological features and are increasingly understood as a spectrum of fibrotic interstitial lung diseases. ILA, especially subpleural fibrotic subtype, are associated with radiological progression and increased mortality and are clinically important for early risk detection of pulmonary fibrosis. Traction bronchiectasis/bronchiolectasis index (TBI) is particularly valuable to further stratify the prognosis of ILA individuals.

Summary

To improve the prognosis of patients with pulmonary fibrosis, further advances in a multifaceted approach to understand the spectrum of pulmonary fibrosis and stratify the risk of progression to pulmonary fibrosis in ILA individuals are warranted.
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Metadata
Title
Interstitial Lung Abnormalities (ILA) and Pulmonary Fibrosis
Authors
Noriaki Wada
Kyung Soo Lee
Hiroto Hatabu
Publication date
02-04-2024
Publisher
Springer US
Published in
Current Pulmonology Reports
Electronic ISSN: 2199-2428
DOI
https://doi.org/10.1007/s13665-024-00350-3
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