Atypical giant cell arteritis presentations diagnosed with FDG-18 whole body PET imaging
Nimal Vijayaraghavan1, Jaye Martin2, Waranga Jayawickrama3
1Department of General Medicine, Rockingham General Hospital, Cooloongup, Western Australia, Australia nimalv19@gmail.com.
Abstract:
Two male patients aged above 70 years were investigated for chronic non-specific symptoms and evidence of significant systemic inflammation, but without classic 'cranial symptoms' of giant cell arteritis (GCA). Each patient had multiple non-diagnostic investigations, but finally extensive large-vessel vasculitis was revealed by whole body positron emission tomography/CT imaging. Both cases were confirmed to have GCA on temporal artery biopsy and responded well to initial high-dose prednisolone therapy. The patients successfully completed 12 months of steroid-sparing therapy with tocilizumab and achieved remission of their condition.
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