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Updated: Jun 10, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
[Idiopathic interstitial pneumonias in 7 children]
Jin-rong Liu1, Yun Peng, Chun-ju Zhou
1Department of Internal Medicine, Beijing Children's Hospital Affiliated to the Capital Medical University, Beijing 100045, China.
Idiopathic interstitial pneumonias (IIPs) in children, including cryptogenic organizing pneumonia (COP/BOOP), usual interstitial pneumonia (UIP), and nonspecific interstitial pneumonia (NSIP), were studied in China. Prognosis varied by IIP type, with steroids being a primary treatment.
Area of Science:
- Pediatric Pulmonology
- Respiratory Medicine
- Interstitial Lung Diseases
Context:
- Idiopathic interstitial pneumonias (IIPs) are increasingly diagnosed in children.
- Understanding the specific types and outcomes of IIPs in pediatric populations in China is limited.
Purpose:
- To investigate the types and prognosis of idiopathic interstitial pneumonias (IIPs) in children in China.
- To analyze clinical, radiologic, and pathologic features of pediatric IIPs.
Summary:
- Seven pediatric patients with IIPs were retrospectively studied, diagnosed with cryptogenic organizing pneumonia/bronchiolitis obliterans organizing pneumonia (COP/BOOP), usual interstitial pneumonia (UIP), or nonspecific interstitial pneumonia (NSIP).
- Chronic cough was the primary symptom. Treatment with prednisone was initiated, with varying responses depending on the IIP subtype.
- COP/BOOP showed complete resolution, NSIP had partial improvement, and UIP showed limited response to treatment.
Impact:
- This study clarifies the spectrum of IIPs in Chinese children, aiding in diagnosis and management.
- It highlights the importance of clinical-radiologic-pathologic correlation for accurate IIP typing in pediatric cases.
- Findings suggest that steroid therapy is a first-line treatment, but prognosis differs significantly among IIP types in children.
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