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Published on: August 19, 2020
Idiopathic collapsing glomerulopathy: A clinicopathologic analysis of 30 cases
1Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Insights
Idiopathic collapsing glomerulopathy (CG) affects both children and adults, presenting distinct clinicopathologic features. Early diagnosis is crucial for managing this significant cause of renal dysfunction.
Area of Science:
- Nephrology
- Pathology
- Pediatrics
Background:
- Collapsing glomerulopathy (CG) is a severe kidney disease linked to infections, drugs, and ischemia.
- Reports of CG in India are infrequent, necessitating local data.
Purpose of the Study:
- To investigate the clinicopathologic features of idiopathic CG in Indian patients.
- To compare adult-onset versus childhood CG.
Main Methods:
- Retrospective analysis of 30 idiopathic CG cases diagnosed between 2006-2009.
- Review of clinical data, laboratory findings, and renal biopsy histology.
- Statistical comparison between pediatric and adult cohorts.
Main Results:
- Childhood CG cases showed longer symptom duration and lower serum creatinine/urea.
- Tubular atrophy and interstitial fibrosis were common histopathologic findings.
- Pediatric CG exhibited more segmental glomerulosclerosis; 9/30 patients progressed to end-stage renal disease.
Conclusions:
- Idiopathic CG significantly impacts renal function in both pediatric and adult populations.
- Clinicopathologic differences exist between childhood and adult-onset CG.
- Prompt diagnosis and management are essential for optimal patient outcomes.
Abstract:
Collapsing glomerulopathy (CG) is a distinct clinicopathologic entity associated with various infections, medications and acute ischemia. There have been few scattered reports of CG from India. This study aimed at evaluating the clinicopathologic features of idiopathic CG in Indian patients with comparison between adult-onset and childhood CG. This study included all cases of idiopathic CG diagnosed over a period of 4 years (2006-2009). Appropriate clinical details and laboratory findings were retrieved. Renal biopsies were reviewed and detailed pathologic features assessed. Statistical analysis was performed to compare various features between adult-onset and childhood CG. Over these 4 years, 30 cases of idiopathic CG were diagnosed. Of these, 11 were children. Childhood CG cases had longer duration of symptoms and lower serum urea and creatinine levels compared with adult patients. In renal histology, tubular atrophy and interstitial fibrosis was frequent in our cases. Pediatric cases of CG showed a higher proportion of segmental glomerulosclerosis. On clinical follow-up, nine of the 30 patients progressed to end-stage renal disease and these included two pediatric patients. Idiopathic CG is a significant cause of renal dysfunction in both pediatric and adult patients. Childhood and adult-onset CG differ in few clinicopathologic features. Early and accurate diagnosis of CG is imperative for appropriate management of these patients.
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