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Updated: Jun 15, 2025

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Approach to diagnosing and managing granulomatous-lymphocytic interstitial lung disease
Jessica Galant-Swafford1, Jason Catanzaro2, Rosane Duarte Achcar3
1Department of Medicine, Division of Allergy and Immunology, National Jewish Health, 1400 Jackson Street, Denver, CO 80206, USA.
Granulomatous-lymphocytic interstitial lung disease (GLILD) is a lung condition linked to primary immune deficiencies. A multidisciplinary approach is crucial for diagnosing and managing GLILD effectively.
Area of Science:
- Pulmonology
- Immunology
- Pathology
Background:
- Granulomatous-lymphocytic interstitial lung disease (GLILD) is a significant pulmonary complication in primary immune deficiencies, particularly common variable immunodeficiency (CVID).
- GLILD contributes substantially to patient morbidity and mortality.
- Early and accurate diagnosis is essential for effective management.
Purpose of the Study:
- To provide a practical framework for diagnosing and evaluating suspected GLILD cases.
- To emphasize the importance of a multidisciplinary team approach in managing GLILD.
- To integrate clinical, radiological, and pathological features into a diagnostic algorithm.
Main Methods:
- Review of key clinical, radiological, and pathological features of GLILD.
- Development of a diagnostic algorithm based on integrated features.
- Emphasis on multidisciplinary team discussion for diagnosis and treatment confidence.
Main Results:
- The review synthesizes current knowledge on GLILD diagnosis and management.
- A diagnostic algorithm is proposed to facilitate consensus diagnosis.
- Limited evidence necessitates a practical, consensus-driven approach.
Conclusions:
- A multidisciplinary approach is paramount for diagnosing and managing GLILD.
- The proposed framework aids in evaluating suspected GLILD cases.
- Further research is needed to address current evidence limitations in GLILD care.
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