sCD25 as an independent adverse prognostic factor in adult patients with HLH: results of a multicenter retrospective study

Hemophagocytic lymphohistiocytosis (HLH) is a rare but often fatal hyperinflammatory syndrome caused by an inborn or acquired error of immunity. In adults, the underlying immunodeficiency generally arises alongside severe infections, malignancies, autoimmune diseases, and immunosuppressive treatment...

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Detalles Bibliográficos
Autores principales: Wimmer, Thomas, Mattes, Raphael, Stemmler, Hans-Joachim, Hauck, Fabian, Schulze-Koops, Hendrik, Stecher, Stephanie-Susanne, Starck, Michael, Wendtner, Clemens-Martin, Bojko, Peter, Hentrich, Marcus, Nickel, Katharina E., Götze, Katharina S., Bassermann, Florian, von Bergwelt-Baildon, Michael, Spiekermann, Karsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Hematology 2022
Materias:
Clinical Trials and Observations
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986715/
https://www.ncbi.nlm.nih.gov/pubmed/35973195
http://dx.doi.org/10.1182/bloodadvances.2022007953

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986715/
https://www.ncbi.nlm.nih.gov/pubmed/35973195
http://dx.doi.org/10.1182/bloodadvances.2022007953

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