Deciphering the clinical profile and diagnostic framework of hemophagocytic lymphohistiocytosis in a tertiary care setting

Background: Hemophagocytic lymphohistiocytosis (HLH) is a severe hyperinflammatory disorder marked by intense yet ineffective immune activation, resulting in hemophagocytosis, systemic inflammation, and multi-organ dysfunction. The diagnosis has traditionally depended on the 2004 HLH criteria, while...

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Detalhes bibliográficos

Principais autores:	Lipsa Priyadarshini, Meenakshi Mohapatro, Priyadarshini Biswal, Silla Alisha Patro, Devidutta Ramani Ranjan Rout, Simadri Swetapadma Roul
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Wolters Kluwer Medknow Publications 2024-12-01
coleção:	MGM Journal of Medical Sciences
Assuntos:	hemophagocytic lymphohistiocytosis hlh criteria hscore
Acesso em linha:	https://doi.org/10.4103/mgmj.mgmj_321_24
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