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Updated: Jun 5, 2026
04:44
Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
[Idiopathic interstitial pneumonia: classification and diagnostic work-up].
Thierry Rochat1, Jean-Claude Pache
1Service de pneumologie, HUG, 1211 Genève 14. thierry.rochat@hcuge.ch
Revue Medicale Suisse
|January 7, 2011
Summary
Idiopathic interstitial pneumonias (IIPs) are complex lung diseases. Accurate diagnosis, confirmed by multidisciplinary teams, is crucial for patient prognosis and treatment.
Area of Science:
- Pulmonology
- Respiratory Medicine
- Interstitial Lung Diseases
Context:
- Idiopathic interstitial pneumonias (IIPs) encompass several complex lung diseases.
- Key types include idiopathic pulmonary fibrosis (IPF), idiopathic non-specific interstitial pneumonia (idiopathic NSIP), and cryptogenic organizing pneumonia (COP).
- Diagnosis relies on established classifications, such as the 2002 America-European consensus.
Purpose:
- To highlight the importance of accurate classification and diagnosis of IIPs.
- To emphasize the necessity of multidisciplinary team (MDT) discussion for confirming diagnoses.
- To underscore the significant impact of correct diagnosis on patient outcomes.
Summary:
- IIPs are a group of challenging lung conditions.
- Accurate classification, often guided by the 2002 America-European consensus, is essential.
- Diagnosis confirmation through experienced multidisciplinary team discussion is critical.
Impact:
- Correctly diagnosing IIPs ensures appropriate patient management.
- Prognostic and therapeutic decisions are heavily influenced by accurate diagnosis.
- Improved patient care through precise identification of specific IIP subtypes.
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