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Updated: Jun 15, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
[Update on non-specific interstitial pneumonia: a pattern, a clinical entity or different phenotypes? Surgical or
Micaela Romagnoli1, Venerino Poletti
1Unità Operativa di Pneumologia Interventistica, Dipartimento di Malattie del Torace, Ospedale G.B. Morgagni-L. Pierantoni, Forli. m.romagnoli@ausl.fo.it
Abstract:
Nonspecific interstitial pneumonia (NSIP) was initially defined in 1994 as a histopathologic pattern, characterized by the presence of varying proportions of lung interstitial inflammation and fibrosis, with a temporally uniform lung involvement, that can be found in the presence of a wide variety of clinical and radiologic contexts. Idiopathic NSIP, considered as a "provisional clinical diagnosis" until recently, has now been recognized as a distinct clinical entity, interestingly occurring mostly in middle-aged and never-smoker women, with dyspnoea, cough, ground glass at high resolution CT scan of the chest, and with a very good prognosis. Though this recent evidence, the diagnosis of idiopathic NSIP is still based on histology obtained from surgical lung biopsy, as recommended by the American Thoracic Society/European Respiratory Society statement: are less invasive procedures, such as transbronchial lung biopsies and bronchoalveolar lavage, useful tools in the initial approach of this clinical entity?
Insights
Nonspecific interstitial pneumonia (NSIP) is a distinct clinical entity, often affecting women and characterized by inflammation and fibrosis. This study questions if less invasive diagnostic methods are sufficient for idiopathic NSIP.
Area of Science:
- Pulmonology
- Pathology
- Radiology
Context:
- Nonspecific interstitial pneumonia (NSIP) was defined as a histopathologic pattern in 1994.
- Idiopathic NSIP is now recognized as a distinct clinical entity, primarily affecting middle-aged, never-smoker women.
- Clinical presentation includes dyspnea, cough, and characteristic ground-glass opacities on CT scans, with a generally good prognosis.
Purpose:
- To evaluate the utility of less invasive diagnostic procedures for idiopathic NSIP.
- To determine if transbronchial lung biopsies and bronchoalveolar lavage are adequate for initial diagnosis.
- To assess the role of these methods in the context of current diagnostic recommendations.
Summary:
- Idiopathic NSIP is characterized by interstitial inflammation and fibrosis with a uniform temporal pattern.
- Diagnosis currently relies on surgical lung biopsy, as per ATS/ERS guidelines.
- The study investigates the potential of transbronchial lung biopsies and bronchoalveolar lavage as initial diagnostic tools.
Impact:
- This research could lead to less invasive diagnostic approaches for idiopathic NSIP.
- Findings may influence clinical guidelines regarding the initial evaluation of suspected NSIP.
- Improved diagnostic strategies could reduce patient morbidity associated with surgical lung biopsies.
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