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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Detalles Bibliográficos
Autor principal: George, Melissa R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Review
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

Internet

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

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