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Hemophagocytic lymphohistiocytosis in adults: An under recognized entity
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of severe immune activation with macrophage and T-cell infiltration resulting in, multi organ damage. HLH may be primary or secondary in etiology. A high index of suspicion is essential for early diagnosis and treatment. Diagnostic criteria need...
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| Veröffentlicht in: | BBA Clin |
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| Hauptverfasser: | , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Elsevier
2016
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5219626/ https://ncbi.nlm.nih.gov/pubmed/28070498 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbacli.2016.12.002 |
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