Abstract
Granulomatosis with polyangiitis (GPA) is a type of antineutrophil cytoplasmic antibody-associated vasculitis, a rare disorder affecting small vessels, primarily the respiratory tracts and the kidneys, with less common involvement of the central nervous system. Although posterior reversible encephalopathy syndrome (PRES) and intracranial hemorrhage (ICH) are documented complications, their concomitant occurrence in adults is extremely rare in this condition. We report a case of a 42-year-old Malay woman with heterozygous hemoglobin constant spring who presented with prolonged fever and recurrent severe anemia, posing a diagnostic dilemma. The diagnosis of GPA was confirmed through renal biopsy, and treatment was initiated. After a brief improvement, she developed status epilepticus secondary to concurrent PRES and ICH. This case highlights the diagnostic challenges of GPA and the rare, simultaneous occurrence of PRES and ICH, warranting careful therapeutic consideration due to both the disease and the treatment complications.
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Article Type: Case Report
ELECTRON J GEN MED, Volume 22, Issue 4, August 2025, Article No: em671
https://doi.org/10.29333/ejgm/16569
Publication date: 07 Jul 2025
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