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Haemophagocytic lymphohisticytosis—an underrecognized hyperinflammatory syndrome
Haemophagocytic lymphohisticytosis (HLH) is a syndrome of uncontrolled, severe systemic inflammation (hyperinflammation) arising either from a genetic immune system defect [primary (pHLH)] or triggered as a complication of malignancy, infection, or rheumatologic disease [secondary (sHLH)]. Patients...
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| Veröffentlicht in: | Rheumatology (Oxford) |
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| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Oxford University Press
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6878843/ https://ncbi.nlm.nih.gov/pubmed/31769857 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/rheumatology/kez379 |
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