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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| Prif Awduron: | , , , , , , , , , , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
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BMC
2025-06-01
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| Cyfres: | Pediatric Rheumatology Online Journal |
| Pynciau: | |
| Mynediad Ar-lein: | https://doi.org/10.1186/s12969-025-01115-1 |
| Tagiau: |
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