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Extranodal NK/T cell lymphoma-associated hemophagocytic syndrome: where do we stand?

   
@article{AOL4525,
	author = {Rui Huang and Ying-Zhi He and Qiu-Yu Lai and Liang Wang},
	title = {Extranodal NK/T cell lymphoma-associated hemophagocytic syndrome: where do we stand?},
	journal = {Annals of Lymphoma},
	volume = {2},
	number = {5},
	year = {2018},
	keywords = {},
	abstract = {Hemophagocytic lymphohistiocytosis (HLH), first reported as “familial hemophagocytic reticulosis” by Farquhar JW in 1952, is a rare life-threatening disorder characterized by overwhelming immune and inflammation activation, and “cytokine storm” (1-5). HLH can be roughly categorized as primary HLH (pHLH), which is inherited, or secondary HLH (sHLH) occurring in a context of infection, autoimmune diseases or malignancies.},
	issn = {2616-2695},	url = {https://aol.amegroups.org/article/view/4525}
}