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GRANULOMATOSIS WITH POLYANGIITIS: THE TRIGGER CANNOT BE LONG HIDDEN

SHAMEEK GAYEN, DİANA ZHANG, ELİZA STERNLİCHT, DANİEL BULANOWSKİ, MAHER TABBA

European Journal of Rheumatology - 2022;9(1):54-57

Department of Medicine, Tufts Medical Center, Tufts University School of Medicine, Boston, Massachusetts, USA

 

Granulomatosis with polyangiitis, or GPA, is a form of vasculitis that affects multiple organs especially the respiratory tract and the kidneys. The diagnosis is suspected with the clinical presentation and elevated serum titer of antineutrophil cytoplasmic antibodies and confirmed with the biopsy of the affected organ. Viral infection has been described as one of the triggers of the immune system in developing GPA. In this report, we describe a rare case of GPA that developed following cytomegalovirus infection in a patient with unknown immunocompromised medical condition.