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Hemophagocytic lymphohistiocytosis: review of etiologies and management
Hemophagocytic lymphohistiocytosis (HLH) covers a wide array of related life-threatening conditions featuring ineffective immunity characterized by an uncontrolled hyperinflammatory response. HLH is often triggered by infection. Familial forms result from genetic defects in natural killer cells and...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062561/ https://www.ncbi.nlm.nih.gov/pubmed/24966707 http://dx.doi.org/10.2147/JBM.S46255 |