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Development of a Neonatal Piglet Acute Lung Injury Model Recreating the Early Environment of Preterm Infant Lungs
Published on: October 31, 2025
Pediatric interstitial lung disease
D Vijayasekaran1, S Giridhar, N C Gowrishankar
1Department of Pulmonology, Institute of Child Health and Hospital for Children, Chennai 600 008, Tamil Nadu, India. vijsekar@hotmail.com
Insights
Interstitial lung diseases (ILD) in children present with cough and dyspnea. High-resolution computed tomography (HRCT) and lung biopsies aid diagnosis, with a mean survival of 2 years and 7 months.
Area of Science:
- Pediatric Pulmonology
- Radiology
- Pathology
Background:
- Interstitial lung diseases (ILD) are a heterogeneous group of disorders affecting lung parenchyma.
- Pediatric ILD diagnosis can be challenging due to varied presentations and limited research.
Purpose of the Study:
- To investigate the clinical features, diagnostic methods, and outcomes of ILD in pediatric patients.
- To analyze symptomatology, radiological findings, and histopathological results in children with ILD.
Main Methods:
- Retrospective analysis of medical records for 16 children diagnosed with ILD between June 2000 and May 2004.
- Evaluation of clinical data, chest X-rays, High-Resolution Computed Tomography (HRCT), bronchoalveolar lavage (BAL), and lung biopsy findings.
Main Results:
- Acute presentation occurred in 25% of cases; Velcro crackles were the most common finding (93.8%).
- HRCT was diagnostic in 86.6% of cases. Spirometry indicated restrictive ventilatory defects in 5 cases.
- BAL showed increased neutrophils, and lung biopsies were consistent with idiopathic pulmonary fibrosis in 5 cases.
Conclusions:
- ILD in children presents with significant respiratory symptoms and characteristic radiological findings.
- A combination of HRCT, BAL, and lung biopsy is crucial for accurate diagnosis and management of pediatric ILD.
- The mean survival duration observed was 2 years and 7 months post-diagnosis.
Abstract:
This study was done to ascertain the symptomatology, clinical features and investigations pertaining to interstitial lung diseases (ILD) in children. The medical records of 16 children admitted over a 4-year period from June 2000 to May 2004 with progressive cough, dyspnea, and chest X-ray/High Resolution Computerized Tomography (HRCT) abnormalities suggesting ILD were retrospectively evaluated. Clinical findings, investigations, chest skiagrams, HRCT, bronchoalveolar lavage (BAL) and lung biopsy reports were analyzed. An acute presentation of symptoms was seen in 4 cases (25%). Velcro crackles were the commonest clinical finding, present in 15 cases (93.8%). Serial X-rays revealed findings suggestive of ILD in 12 cases (75%) and HRCT was diagnostic in 13 cases (86.6%). Spirometry done in 5 cases showed a restrictive ventilatory defect, BAL analysis done in 8 cases demonstrated increased neutrophils and lung biopsy done in 5 cases was consistent with idiopathic pulmonary fibrosis. Mean survival duration of 2 years and 7 months after initial diagnosis was observed.
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