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Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
Lupus nephritis in children
Farkhanda Hafeez1, Abid Mahmood Tarar, Rashid Saleem
1Department of Nephrology, The Children's Hospital and Institute of Child Health, Lahore,Pakistan. drfarkh@hotmail.com
Insights
Lupus nephritis in children commonly presents with diffuse proliferative glomerulonephritis. Early immunosuppressive therapy effectively controls this condition in most pediatric nephrology patients.
Area of Science:
- Pediatric Nephrology
- Immunology
- Rheumatology
Background:
- Lupus nephritis is a severe renal complication of Systemic Lupus Erythematosus (SLE).
- Understanding the clinicopathological patterns in pediatric patients is crucial for effective management.
Purpose of the Study:
- To determine the clinicopathological pattern of lupus nephritis in pediatric nephrology patients.
- To analyze the histological lesions, clinical manifestations, and treatment outcomes.
Main Methods:
- A case series study was conducted in a pediatric nephrology department over five years.
- Twenty-six pediatric patients (up to 16 years) with primary SLE and renal involvement were included.
- Percutaneous renal biopsies were performed, and histological lesions were classified using WHO criteria.
Main Results:
- Diffuse proliferative glomerulonephritis was the most common histological lesion (n=14), followed by membranous nephropathy (n=6).
- Edema (80.76%) and hypertension (46.15%) were the most frequent clinical manifestations.
- Proteinuria was universal (100%), while azotemia occurred in 19.33% of patients. Disease control was achieved in 73.07% with immunosuppressive therapy.
Conclusions:
- Diffuse proliferative glomerulonephritis is the predominant histological finding in pediatric lupus nephritis in this cohort.
- Renal involvement typically manifests within two years of SLE onset and is manageable with immunosuppressive therapy.
Objective:
To determine the clinicopathological pattern of lupus nephritis in paediatric nephrology patients.
Design:
Case series study.
Place And Duration Of Study:
The department of paediatric nephrology at the Children's Hospital and Institute of Child Health, Lahore, Pakistan, over a period of five years from January 2001 to December 2005.
Patients And Methods:
Twenty six patients upto the age 16 years of either gender, with a mean age of 12.4 +/- 1.90 years having primary SLE with renal involvement in the form of oedema, hypertension, haematuria and proteinuria were included. Twenty one were females. Percutaneous renal biopsy was performed. Histological lesion was classified according to WHO classification. Patients were treated with immunosuppressive therapy and their clinical course was followed for at least one year. The mean duration of follow up was 1.77 years.
Results:
Renal involvement was seen in 92.30% within 2 years of the onset of primary disease. Diffuse proliferative glomerulonephritis was the commonest histological lesion (n=14) followed by membranous nephropathy (n=6). The commonest clinical manifestation was oedema (80.76%) followed by hypertension (46.15%). Proteinuria was present in 100% of cases, haematuria in 38.46% and azotemia in 19.33% of patients. Nephrotic range proteinuria was more common in class III and IV, while azotemia was observed only in class IV. The disease was well controlled in 73.07% , relapse was seen in 3.8% of patients, 15.38% died of infections and uremic encephalopathy while 7.69% were lost to follow-up.
Conclusion:
Diffuse proliferative glomerulonephritis is the commonest histological lesion in our set-up. Renal involvement is mostly seen within first two years of the primary disease which can be controlled satisfactorily with immunosuppressive therapy.
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