Hemophagocytic lymph histiocytosis (HLH): etiologies, pathogenesis, treatment, and outcomes in critically ill patients: a review article and literature to review

Hemophagocytic lymph histiocytosis (HLH) is not an independent disease but is instead a clinical syndrome that occurs in many underlying conditions involving all age groups. HLH is the consequence of a severe, uncontrolled hyperinflammatory reaction that in most cases is triggered by an infectious a...

Descripción completa

Detalles Bibliográficos
Autores principales: Mirza, Mohsin, Zafar, Maryam, Nahas, Joseph, Arshad, Wafa, Abbas, Anum, Tauseef, Abubakar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8462863/
https://www.ncbi.nlm.nih.gov/pubmed/34567455
http://dx.doi.org/10.1080/20009666.2021.1954783

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8462863/
https://www.ncbi.nlm.nih.gov/pubmed/34567455
http://dx.doi.org/10.1080/20009666.2021.1954783

Ejemplares similares