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Updated: May 17, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Granulomatous lymphocytic interstitial lung disease
1Autoimmune Lung Center and Interstitial Lung Disease Program, Division of Pulmonary and Critical Care Medicine, National Jewish Health, B'nai B'rith Building, Office #M322, 1400 Jackson Street, Denver, CO 80206, USA. fernandezevans@njhealth.org
The incidence of granulomatous-lymphocytic interstitial lung disease (GLILD), a noninfectious disorder, is rising with increased use of intravenous gamma globulin. Accurate diagnosis and management are crucial for this condition.
Area of Science:
- Immunology
- Pulmonology
- Rheumatology
Background:
- The use of high-dose intravenous gamma globulin and antimicrobials is increasing.
- This rise is associated with a growing incidence of noninfectious common variable immunodeficiency-related disorders.
- Granulomatous-lymphocytic interstitial lung disease (GLILD) is a notable example of such a disorder.
Purpose of the Study:
- To provide a comprehensive overview of the diagnosis and management of GLILD.
- To highlight the importance of a multidisciplinary approach in diagnosing GLILD.
- To emphasize the need for further research and data collection on GLILD.
Main Methods:
- Review of current clinical understanding and diagnostic approaches for GLILD.
- Discussion of management strategies based on existing literature and clinical experience.
- Emphasis on the necessity of multidisciplinary care models.
Main Results:
- GLILD diagnosis requires thorough clinical evaluation.
- Multidisciplinary care models are essential for accurate GLILD diagnosis.
- Therapeutic trials for GLILD are becoming feasible due to recent advancements in understanding.
Conclusions:
- The incidence of GLILD is expected to increase.
- Accurate diagnosis and effective management are critical for patients with GLILD.
- Further data from registries and population-based studies are needed to understand GLILD trends and burden.
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