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Benralizumab: A novel treatment for the cutaneous features of paediatric eosinophilic granulomatosis with polyangiitis (pEGPA).

Abstract
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis presenting primarily with pulmonary and cutaneous features. The disease is typically seen in the fifth or sixth decade of life (1, 2). We report a case of EGPA in an adolescent who was successfully treated with the interleukin-5 (IL-5) receptor inhibitor, benralizumab.
AuthorsM Bandla, M Howard, A McNally, D Armstrong, I Simpson, A Mar
JournalThe Australasian journal of dermatology (Australas J Dermatol) Vol. 64 Issue 3 Pg. 404-407 (Aug 2023) ISSN: 1440-0960 [Electronic] Australia
PMID37195732 (Publication Type: Case Reports, Journal Article)
Copyright© 2023 Australasian College of Dermatologists.
Chemical References
  • benralizumab
  • Antibodies, Monoclonal, Humanized
Topics
  • Adolescent
  • Humans
  • Child
  • Granulomatosis with Polyangiitis (drug therapy)
  • Churg-Strauss Syndrome (drug therapy)
  • Antibodies, Monoclonal, Humanized (therapeutic use)

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