Hemophagocytic Lymphohistiocytosis (HLH) in a Patient with Disseminated Histoplasmosis

Hemophagocytic lymphohistiocytosis (HLH) is a rare condition characterized by an overwhelming inflammatory cascade activation which is often associated with rapid progression and high mortality. It may be familial with an underlying genetic mutation or triggered by infection, malignancy, and autoimm...

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Detalles Bibliográficos
Autores principales: Swaminathan, Neeraja, Vinicius, Jorge M., Serrins, Jesse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387958/
https://www.ncbi.nlm.nih.gov/pubmed/32765915
http://dx.doi.org/10.1155/2020/5638262

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387958/
https://www.ncbi.nlm.nih.gov/pubmed/32765915
http://dx.doi.org/10.1155/2020/5638262

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