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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Detalles Bibliográficos
Autores principales: Hutchinson, Matthew, Tattersall, Rachel S, Manson, Jessica J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Supplement Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878843/
https://www.ncbi.nlm.nih.gov/pubmed/31769857
http://dx.doi.org/10.1093/rheumatology/kez379

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878843/
https://www.ncbi.nlm.nih.gov/pubmed/31769857
http://dx.doi.org/10.1093/rheumatology/kez379

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