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Case Report: Polyarteritis nodosa or complicated Henoch-Schonlein purpura (IgAV), a rare case
Background: Polyarteritis nodosa (PAN) is a vasculitis that affects medium-sized arteries. PAN is a rare disease and requires a high clinical suspicion for diagnosis. PAN and HSP (newly named Immunoglobulin A-associated vasculitis) have narrowing differential diagnosis. Here, we reported a case of P...
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| Publicat a: | F1000Res |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
F1000 Research Limited
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5930546/ https://ncbi.nlm.nih.gov/pubmed/29770208 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.13295.2 |
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