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Granulomatosis with Polyangiitis Misdiagnosed as IgA Vasculitis in a Child
BACKGROUND: Granulomatosis with polyangiitis (GPA) with early manifestations simulating IgA vasculitis is a very rare childhood systemic disease. Case Presentation. A 10-year-old boy presented initially with cutaneous, skeletal, and abdominal signs suggestive of IgA vasculitis. Over time, the worsen...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10125763/ https://www.ncbi.nlm.nih.gov/pubmed/37102146 http://dx.doi.org/10.1155/2023/9950855 |