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ZyraDoc #47 - September 17, 2026

#46

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#48

A 26-year-old female presents with a 2-month history of worsening bilateral hand joint pain, fatigue, a persistent malar rash spanning her nasal bridge and cheeks, and progressive swelling in both lower extremities.

Laboratory evaluation reveals a positive antinuclear antibody (ANA 1:1280), high titers of anti-double-stranded DNA (anti-dsDNA) antibodies, reduced complement levels (C3 and C4), elevated serum creatinine (1.9 mg/dL), and subnephrotic proteinuria (2.4 g/24 hr).

A renal biopsy demonstrates Diffuse Proliferative Glomerulonephritis (Class IV Lupus Nephritis) with subendothelial immune complex deposits and hypercellularity.

Case Summary

Clinical Focus:

  • The diagnosis is Systemic Lupus Erythematosus (SLE) with Class IV Lupus Nephritis.

Aetiology/Cause:

  • Systemic autoimmune disease characterized by loss of self-tolerance, nuclear autoantigen exposure, and autoantibody production.
  • Deposition of circulating antinuclear immune complexes (specifically anti-dsDNA) within the renal glomerular basement membrane and mesangium.
  • Activation of the classical complement cascade triggering intense inflammatory cell recruitment, microvascular endothelial damage, and glomerular proliferation.

Clinical Features:

  • Constitutional and systemic features including persistent fatigue, low-grade fever, weight loss, and symmetrical inflammatory polyarthralgia.
  • Dermatological manifestations such as a photosensitive malar (butterfly) rash, discoid lesions, and oral/nasal ulcers.
  • Renal involvement manifesting as peripheral edema, hypertension, hematuria with dysmorphic red blood cells or RBC casts, and proteinuria.
  • Multisystem engagement including serositis (pleuritis, pericarditis), hematologic cytopenias, and neuropsychiatric symptoms.

Diagnosis and Investigations:

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