Abstract
Immunoglobulin G4-related disease (IgG4-RD) is a systemic immune-mediated fibroinflammatory condition characterized by tumefactive lesions that can affect multiple organs. Serum IgG4 levels may be elevated. Early recognition is sometimes difficult but is important to avoid irreversible organ damage. We describe the case of a 28-year-old male patient who presented with a 2-year history of recurrent low-grade fever, night sweats and non-specific manifestations. We eventually diagnosed IgG4-related aortitis by PET-CT scan. The patient was successfully treated with prednisolone and mycophenolate mofetil with complete clinical and radiological resolution.
Author supplied keywords
Cite
CITATION STYLE
Fong, C. W., Lio, L. I., Pon, M., Mok, T. M., & Hou, N. (2018). IgG4-related aortitis. European Journal of Case Reports in Internal Medicine, 5(9). https://doi.org/10.12890/2018_000881
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.