What is the diagnosis and management for a patient with facial edema, albuminuria (proteinuria) of 2+, hematuria with dysmorphic Red Blood Cells (RBCs), normal Complement 3 (C3) levels, elevated Anti-Streptolysin O (ASO) titer, and normal blood pressure?

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Diagnosis: Post-Streptococcal Glomerulonephritis (PSGN)

This patient has post-streptococcal glomerulonephritis (PSGN), and the primary management is supportive care with close monitoring, as immunosuppressive therapy is not indicated for typical PSGN. 1, 2, 3

Clinical Reasoning

The constellation of findings strongly points to PSGN:

  • Facial edema with albuminuria (2+) indicates glomerular injury with fluid retention 3
  • Hematuria with dysmorphic RBCs confirms glomerular origin of bleeding 4, 5
  • Elevated ASO titer provides serologic evidence of recent streptococcal infection 1, 2, 3
  • Normal C3 is atypical but does not exclude PSGN, as complement levels can normalize by presentation or remain normal in some cases 3
  • Normal blood pressure is reassuring and indicates less severe disease 1, 3

The normal C3 deserves special attention. While classically PSGN presents with low C3, this patient may have presented later in the disease course when complement has normalized, or represents a variant presentation. 3 The elevated ASO with the nephritic picture (hematuria with dysmorphic RBCs) makes PSGN the most likely diagnosis despite normal complement. 2

Differential Considerations

Rule out IgA nephropathy (IgAN): IgAN can present similarly with hematuria, proteinuria, and elevated ASO (during concurrent infection), but typically has normal complement and lacks the acute nephritic presentation with edema. 6 A kidney biopsy would show IgA-dominant immunofluorescence rather than the C3-dominant pattern of PSGN.

Rule out C3 glomerulopathy: The normal C3 makes this less likely, though C3 glomerulonephritis can occasionally present with elevated ASO. 7, 8 However, C3 glomerulopathy typically shows persistent hypocomplementemia and requires biopsy for definitive diagnosis.

Rule out ANCA-associated vasculitis: The normal blood pressure and absence of systemic symptoms make this unlikely. 4, 5 ANCA testing should be performed if there are pulmonary symptoms, sinusitis, or rapidly progressive renal failure.

Management Strategy

Immediate Actions

Supportive care is the cornerstone of PSGN management: 6, 1, 2, 3

  • Sodium restriction to 2 grams daily to manage edema 6
  • Diuretics (loop diuretics preferred) for persistent edema despite sodium restriction 6
  • Monitor fluid balance carefully to avoid volume depletion 6
  • Blood pressure control if hypertension develops, though currently normal 6

Monitoring Parameters

Serial laboratory assessment is essential: 3

  • Renal function (creatinine, GFR) every 2-3 days initially to detect deterioration 3
  • Urinalysis weekly to monitor hematuria and proteinuria resolution 1
  • Repeat C3 level in 1-2 weeks; persistent low C3 beyond 8 weeks suggests alternative diagnosis 3
  • Blood pressure daily until stable 6

When to Consider Biopsy

Kidney biopsy is indicated if: 6

  • Renal function deteriorates (rising creatinine, declining GFR) 6
  • Proteinuria persists beyond 6 months 1
  • Hematuria persists beyond 12-18 months 1
  • C3 remains low beyond 8 weeks 3
  • Clinical course is atypical or severe 6

Immunosuppression: Not Indicated

Do not use corticosteroids or other immunosuppressive agents for typical PSGN. 6, 1, 2 PSGN is a self-limited disease with excellent prognosis, particularly when presenting without severe renal impairment or hypertension. 1, 3 Immunosuppression is reserved for proven chronic glomerulonephritis patterns (like IgAN or crescentic GN) confirmed by biopsy, not for acute post-infectious GN. 6

Renin-Angiotensin System Blockade

ACE inhibitors or ARBs are not routinely indicated in PSGN unless hypertension develops or proteinuria persists beyond the acute phase. 6 Since blood pressure is currently normal and this is acute disease, hold off on RAS inhibition initially. If proteinuria exceeds 1 g/day at 3-6 months follow-up, consider ACE-I/ARB therapy. 6

Prognosis

The prognosis for PSGN is excellent, especially in this patient with normal blood pressure and no severe renal impairment. 1, 3 Most patients achieve complete clinical recovery within weeks to months. 1, 2 Histological resolution may take up to 9 years, but clinical normalization of renal function typically occurs much earlier. 1 Children and young adults have particularly favorable outcomes. 3

Critical Pitfalls to Avoid

Do not delay evaluation if renal function worsens: Rapidly progressive glomerulonephritis (RPGN) can mimic PSGN initially but requires urgent biopsy and immunosuppression. 6, 5 If creatinine rises significantly over days, proceed immediately to biopsy without waiting for "typical" PSGN resolution.

Do not assume all post-streptococcal presentations are benign PSGN: Rare cases can develop crescentic transformation requiring aggressive therapy. 6 The normal blood pressure and modest proteinuria (2+) in this case are reassuring, but vigilance is required.

Do not stop monitoring prematurely: Even with clinical improvement, follow urinalysis for 12-18 months to ensure complete resolution. 1 Persistent abnormalities warrant nephrology referral and possible biopsy. 6

References

Guideline

Vasculitis Clinical Manifestations and Diagnostic Considerations

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Renal Vasculitis Diagnosis and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

A case of C3 glomerulonephritis successfully treated with eculizumab.

Pediatric nephrology (Berlin, Germany), 2015

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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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