• Gareth Lim, Sheryl Lim, Shang-Ian Tee, and Chai Yiing Ling.
• Internal Medicine, Khoo Teck Puat Hospital, National Healthcare Group, Singapore.
• BMJ Case Rep. 2019 Jul 10; 12 (7).

AbstractEosinophilic granulomatosis with polyangiitis (EGPA) is a multisystemic small-vessel vasculitic disease that can present with positive MPO-P-ANCA (myeloperoxidase-perinuclear-anti-neutrophil cytoplasmic antibody). It is a rare condition that is difficult to diagnose. We present the case of a 64-year-old man with late-onset adult asthma and treated nasopharyngeal carcinoma who initially presented to us with proximal myopathy. Thereafter, he developed a constellation of fleeting symptoms which included rhinosinusitis, mononeuritis multiplex, skin vasculitis and arthritis. Blood investigations showed that he had eosinophilia, and skin biopsy demonstrated dermal vasculitis with eosinophils. He was found to be MPO-C-ANCA positive, and although initially thought to have granulomatosis with polyangiitis, the diagnosis was later revised to EGPA. This case highlights the diagnostic challenges with atypical presentations of EGPA and also presents a rare case of positive MPO-C-ANCA that has never been described in EGPA before.© BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

19 keywords...

hide…