A systematic review of malignancy-associated hemophagocytic lymphohistiocytosis that needs more attentions

As an infrequent but potentially life-threatening hyperinflammatory syndrome, hemophagocytic lymphohistiocytosis (HLH) is clinically characterized with prolonged fever, hepatosplenomegaly, cytopenia, hypertriglyceridemia, hyperferritinemia and hemophagocytosis in bone marrow, liver, spleen or lymph...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Hongluan, Xiong, Lixia, Tang, Weiping, Zhou, Ying, Li, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601794/
https://www.ncbi.nlm.nih.gov/pubmed/28938698
http://dx.doi.org/10.18632/oncotarget.19230

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601794/
https://www.ncbi.nlm.nih.gov/pubmed/28938698
http://dx.doi.org/10.18632/oncotarget.19230

Ejemplares similares