Current status of the diagnosis and treatment of hemophagocytic lymphohistiocytosis in adults

Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of defective apoptosis, a disruption of the regulatory pathway that terminates immune and inflammatory responses. Fever, cytopenia, splenomegaly, and/or hemophagocytosis are typical findings of this syndrome. HLH can be induced by genetic disord...

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Detalles Bibliográficos
Autores principales: Kim, Yu Ri, Kim, Dae-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094004/
https://www.ncbi.nlm.nih.gov/pubmed/33935031
http://dx.doi.org/10.5045/br.2021.2020323

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094004/
https://www.ncbi.nlm.nih.gov/pubmed/33935031
http://dx.doi.org/10.5045/br.2021.2020323

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