Chest CT in Pulmonary Fibrosis: A Narrative Review of Imaging Patterns and Their Prognostic Significance

Pulmonary fibrosis represents a heterogeneous group of interstitial lung diseases (ILDs) marked by progressive scarring of the lung parenchyma and declining respiratory function. High-resolution computed tomography (HRCT) plays a pivotal role in diagnosing and managing fibrotic ILDs, particularly id...

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Main Authors: Mehrshad Dabbagh, Mohammad Amin Shajareh Pour Salavati, Yas Zeinaly Parizi
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2025-06-01
Series:Journal of Cardio-Thoracic Medicine
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Online Access:https://jctm.mums.ac.ir/article_26359_86666ae9128bcde8249a6240fd208fc4.pdf
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author Mehrshad Dabbagh
Mohammad Amin Shajareh Pour Salavati
Yas Zeinaly Parizi
author_facet Mehrshad Dabbagh
Mohammad Amin Shajareh Pour Salavati
Yas Zeinaly Parizi
author_sort Mehrshad Dabbagh
collection DOAJ
description Pulmonary fibrosis represents a heterogeneous group of interstitial lung diseases (ILDs) marked by progressive scarring of the lung parenchyma and declining respiratory function. High-resolution computed tomography (HRCT) plays a pivotal role in diagnosing and managing fibrotic ILDs, particularly idiopathic pulmonary fibrosis (IPF), connective tissue disease-associated ILD (CTD-ILD), and chronic hypersensitivity pneumonitis (CHP). This narrative review explores key imaging patterns observable on chest CT and their prognostic implications across these major subtypes. We conducted a literature review of studies published between 2010 and 2025 using PubMed, Scopus, and Web of Science, focusing on CT features, subtype differentiation, prognostic imaging biomarkers, and recent innovations in radiomics and artificial intelligence (AI). Characteristic HRCT findings, such as honeycombing, reticulation, ground-glass opacities, and traction bronchiectasis, were analyzed in the context of usual interstitial pneumonia (UIP) and nonspecific interstitial pneumonia (NSIP) patterns. UIP pattern on HRCT is strongly associated with IPF and confers a worse prognosis compared to NSIP or other non-UIP patterns. Quantitative imaging methods and automated CT analytics offer objective measurements of fibrosis extent and have demonstrated promising correlations with physiologic parameters such as forced vital capacity (FVC) and diffusing capacity for carbon monoxide (DLCO). Emerging AI tools enhance disease classification, monitor progression, and support clinical decision-making. Despite substantial advances, challenges such as inter-reader variability, limited access to quantitative software, and unstandardized CT protocols persist. Furthermore, AI applications require broader validation in multicenter cohorts before routine implementation. This review highlights the central role of HRCT in the multidisciplinary evaluation of pulmonary fibrosis. It underscores the prognostic significance of specific imaging features and advocates for standardized imaging interpretation and the integration of AI to refine diagnostic accuracy and therapeutic planning.
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spelling doaj-art-8b43bb892f3448f698ce795e819c26d32025-08-20T03:08:39ZengMashhad University of Medical SciencesJournal of Cardio-Thoracic Medicine2345-24472322-57502025-06-011321545155410.22038/jctm.2025.88917.149226359Chest CT in Pulmonary Fibrosis: A Narrative Review of Imaging Patterns and Their Prognostic SignificanceMehrshad Dabbagh0Mohammad Amin Shajareh Pour Salavati1Yas Zeinaly Parizi2Student Research Committee, School of Medicine, Kerman University of Medical Sciences, Kerman, Iran.Student Research Committee, School of Medicine, Kerman University of Medical Sciences, Kerman, Iran.Student Research Committee, School of Medicine, Kerman University of Medical Sciences, Kerman, Iran.Pulmonary fibrosis represents a heterogeneous group of interstitial lung diseases (ILDs) marked by progressive scarring of the lung parenchyma and declining respiratory function. High-resolution computed tomography (HRCT) plays a pivotal role in diagnosing and managing fibrotic ILDs, particularly idiopathic pulmonary fibrosis (IPF), connective tissue disease-associated ILD (CTD-ILD), and chronic hypersensitivity pneumonitis (CHP). This narrative review explores key imaging patterns observable on chest CT and their prognostic implications across these major subtypes. We conducted a literature review of studies published between 2010 and 2025 using PubMed, Scopus, and Web of Science, focusing on CT features, subtype differentiation, prognostic imaging biomarkers, and recent innovations in radiomics and artificial intelligence (AI). Characteristic HRCT findings, such as honeycombing, reticulation, ground-glass opacities, and traction bronchiectasis, were analyzed in the context of usual interstitial pneumonia (UIP) and nonspecific interstitial pneumonia (NSIP) patterns. UIP pattern on HRCT is strongly associated with IPF and confers a worse prognosis compared to NSIP or other non-UIP patterns. Quantitative imaging methods and automated CT analytics offer objective measurements of fibrosis extent and have demonstrated promising correlations with physiologic parameters such as forced vital capacity (FVC) and diffusing capacity for carbon monoxide (DLCO). Emerging AI tools enhance disease classification, monitor progression, and support clinical decision-making. Despite substantial advances, challenges such as inter-reader variability, limited access to quantitative software, and unstandardized CT protocols persist. Furthermore, AI applications require broader validation in multicenter cohorts before routine implementation. This review highlights the central role of HRCT in the multidisciplinary evaluation of pulmonary fibrosis. It underscores the prognostic significance of specific imaging features and advocates for standardized imaging interpretation and the integration of AI to refine diagnostic accuracy and therapeutic planning.https://jctm.mums.ac.ir/article_26359_86666ae9128bcde8249a6240fd208fc4.pdfct scanildaiipfnsip
spellingShingle Mehrshad Dabbagh
Mohammad Amin Shajareh Pour Salavati
Yas Zeinaly Parizi
Chest CT in Pulmonary Fibrosis: A Narrative Review of Imaging Patterns and Their Prognostic Significance
Journal of Cardio-Thoracic Medicine
ct scan
ild
ai
ipf
nsip
title Chest CT in Pulmonary Fibrosis: A Narrative Review of Imaging Patterns and Their Prognostic Significance
title_full Chest CT in Pulmonary Fibrosis: A Narrative Review of Imaging Patterns and Their Prognostic Significance
title_fullStr Chest CT in Pulmonary Fibrosis: A Narrative Review of Imaging Patterns and Their Prognostic Significance
title_full_unstemmed Chest CT in Pulmonary Fibrosis: A Narrative Review of Imaging Patterns and Their Prognostic Significance
title_short Chest CT in Pulmonary Fibrosis: A Narrative Review of Imaging Patterns and Their Prognostic Significance
title_sort chest ct in pulmonary fibrosis a narrative review of imaging patterns and their prognostic significance
topic ct scan
ild
ai
ipf
nsip
url https://jctm.mums.ac.ir/article_26359_86666ae9128bcde8249a6240fd208fc4.pdf
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