Can varicella (chickenpox) cause Post-Infectious Glomerulonephritis (PIGN) in pediatric patients?

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Can Varicella Cause Post-Infectious Glomerulonephritis (PIGN)?

Yes, varicella can cause PIGN, though it is an extremely rare complication. While Group A Streptococcus remains the most common causative agent of PIGN in children, varicella-zoster virus has been documented as a rare infectious trigger for acute glomerulonephritis 1, 2.

Evidence for Varicella-Associated Glomerulonephritis

The association between varicella and glomerulonephritis is well-documented but uncommon:

  • Case reports demonstrate that varicella can trigger membranoproliferative glomerulonephritis with massive proteinuria (up to 16 g/24 hours), gross hematuria, and pyuria 1
  • Most reported cases of post-varicella glomerulonephritis occur in children, though adolescent cases have been documented 1
  • The mechanism appears to be immune complex-mediated hypocomplementemic glomerulonephritis in response to varicella-zoster infection 1

Clinical Context and Epidemiology

Understanding the broader landscape of PIGN helps contextualize varicella as a cause:

  • Non-streptococcal organisms are emerging as important etiological agents of PIGN in high-income countries, expanding beyond the traditional post-streptococcal paradigm 2
  • The spectrum of causative agents for PIGN includes multiple viral and bacterial infections beyond Group A Streptococcus 3
  • Staphylococcal infections are now as common as streptococcal infections in causing PIGN, particularly in adults 4

Clinical Presentation and Prognosis

When varicella does cause glomerulonephritis, the clinical features are important to recognize:

  • Proteinuria in most post-varicella glomerulonephritis cases is benign and self-limiting, though rare fatal cases of crescentic glomerulonephritis progressing to acute renal failure have been reported 1
  • The clinical presentation can vary from asymptomatic microscopic hematuria to rapidly progressive glomerulonephritis requiring dialysis 3
  • Acute proliferative glomerulonephritis typically manifests as immune complex hypocomplementemic disease 1

Important Caveats

Several clinical pitfalls warrant attention:

  • The rarity of this complication means varicella should not be the first suspected cause when evaluating PIGN - streptococcal and staphylococcal infections remain far more common 2, 5
  • Renal involvement during varicella infection is infrequent overall, making this an unusual presentation 1
  • The latency period between infection and nephritis onset (characteristic of PIGN) should be considered when establishing temporal relationships 5

Practical Implications

For immunocompromised patients with nephrotic syndrome who develop varicella:

  • High-dose intravenous acyclovir (10 mg/kg every 8 hours) for 7-10 days is mandatory for treatment 6
  • Post-exposure prophylaxis with varicella-zoster immune globulin (VZIG) should be administered as soon as possible after exposure, effective up to 10 days post-exposure 6
  • If VZIG is unavailable, prophylactic oral acyclovir (10 mg/kg four times daily for 7 days) within 7-10 days of exposure is recommended 7, 6

References

Research

Post-infectious glomerulonephritis.

Paediatrics and international child health, 2017

Research

Infection-Related Glomerulonephritis.

Pediatric clinics of North America, 2019

Guideline

Treatment of Chickenpox in Infants

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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