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Two unique cases of eosinophilic granulomatosis with polyangiitis in childhood treated with anti-interleukin-5 therapy: infantile-onset and submandibular salivary gland involvement

Abstract Background ANCA-associated vasculitis is a systemic autoimmune disease involving small- and medium-sized blood vessels. Eosinophilic granulomatosis with polyangiitis (EGPA, previously Churg Strauss Syndrome) is the least common form in childhood with few cases reported. We present two uniqu...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Evangelia Constantine, Adam M. Bartholomeo, Inna Powers, Jerimiah L. Lysinger, Pia J. Hauk, Jordan Abbott, Heather H. de Keyser, Nicholas J. Gilman, Csaba Galambos, Angus Toland, Nicholas Willard, Jason Weinman, David Mong, Clara Lin, Jessica L. Bloom
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BMC 2025-06-01
Cyfres:Pediatric Rheumatology Online Journal
Pynciau:
Mynediad Ar-lein:https://doi.org/10.1186/s12969-025-01115-1
Tagiau: Ychwanegu Tag
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