Successful Modified Therapy in a Patient with Probable Infection-Associated Hemophagocytic Lymphohistiocytosis

Hemophagocytic lymphohistiocytosis (HLH) is a rare, hyperinflammatory syndrome characterized by clinical signs and symptoms of extreme inflammation. In adults, HLH is typically a complication of infections, autoimmune diseases, and malignancies. While the disease is often fatal, classic management o...

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Detalles Bibliográficos
Autores principales: Kay, Carl L., Rendo, Matthew J., Gonzales, Paul, Beganovic, Sead G., Czader, Magdalena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754915/
https://www.ncbi.nlm.nih.gov/pubmed/31583147
http://dx.doi.org/10.1155/2019/9781065

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754915/
https://www.ncbi.nlm.nih.gov/pubmed/31583147
http://dx.doi.org/10.1155/2019/9781065

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