Adult secondary hemophagocytic lymphohistiocytosis

BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of excessive inflammation and tissue destruction due to abnormal immune activation. HLH carries a very high mortality, and while delays in patients’ presentation to hospital, time to suspicion of HLH, investigation, and initiation of...

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Detalles Bibliográficos
Autores principales: Obayo, Antonina, Sharma, Karishma, Mithi, Caroline, Riyat, Malkit, Mwirigi, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Short Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175838/
https://www.ncbi.nlm.nih.gov/pubmed/35844997
http://dx.doi.org/10.1002/jha2.113

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175838/
https://www.ncbi.nlm.nih.gov/pubmed/35844997
http://dx.doi.org/10.1002/jha2.113

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