Conjunctivitis, episcleritis and anterior uveitis as the first presenting features of granulomatosis with

Lucas Donato Foster1, Michael Nyugen2, Edward Margolin2

  • 1Department of Medicine, University of Western Ontario, London, Ontario, Canada lfoste9@uwo.ca.

BMJ Case Reports
|October 28, 2021
PubMed

Insights

Granulomatosis with polyangiitis (GPA) can initially manifest with eye inflammation and kidney failure. Early diagnosis and treatment, including steroids and rituximab, are crucial for symptom resolution and kidney function recovery.

Area of Science:

  • Ophthalmology
  • Nephrology
  • Rheumatology

Background:

  • Granulomatosis with polyangiitis (GPA) is a rare systemic vasculitis affecting small and medium blood vessels.
  • GPA commonly impacts the respiratory tract and kidneys, but can also involve ocular and renal systems concurrently.

Observation:

  • A 38-year-old male presented with conjunctivitis, episcleritis, and anterior uveitis as initial symptoms.
  • Further investigations revealed acute renal failure, elevated inflammatory markers, and positive c-antineutrophil cytoplasmic antibodies.

Findings:

  • Renal biopsy confirmed necrotizing crescentic glomerulonephritis, leading to a GPA diagnosis.
  • Ocular inflammation and renal dysfunction co-occurred, highlighting a less common GPA presentation.

Implications:

  • This case underscores the importance of considering GPA in patients with simultaneous ocular and renal manifestations.
  • Prompt diagnosis and multi-modal treatment, including immunosuppressants and plasmapheresis, can lead to favorable outcomes in GPA.

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