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Fulminant primary manifestations of Wegener’s granulomatosis might not be pauci-immune
Wegener’s granulomatosis is an ANCA-associated small vessel vasculitis. Because histologically immune complex deposits are frequently lacking, the term pauci-immune has been introduced for this subgroup. We report a patient with fulminant, severe PR3-ANCA-positive Wegener’s granulomatosis and multi-...
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| Udgivet i: | NDT Plus |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2010
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4421412/ https://ncbi.nlm.nih.gov/pubmed/25949469 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ndtplus/sfq145 |
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