Abstract
Eosinophilic granulomatosis with polyangiitis (EGPA) is characterised by many features, including asthma, allergic rhinitis, peripheral and tissue eosinophilia, and vasculitis. Its pathophysiology is still unclear and we suggest that there are different phenotypes of EGPA, which may respond differently to available treatments. Within the most promising targeting biotherapy, benralizumab, an anti-interleukin-5 receptor alpha monoclonal antibody, has proved both highly effective and safe. We report herewith a case of EGPA presenting a myocarditis relapse successfully treated with benralizumab.
Author supplied keywords
Cite
CITATION STYLE
Belfeki, N., Abroug, S., Ghriss, N., Chouchane, I., Hamrouni, S., Strazzulla, A., & Zayet, S. (2022). Successful benralizumab for eosinophilic myocarditis in eosinophilic granulomatosis with polyangiitis. Clinical and Experimental Rheumatology, 40(4), 834–837. https://doi.org/10.55563/clinexprheumatol/ahyqld
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.