Adult haemophagocytic lymphohistiocytosis: a review
2020; Oxford University Press; Volume: 115; Issue: 4 Linguagem: Inglês
10.1093/qjmed/hcaa011
ISSN1460-2725
AutoresHalil Yıldız, Eric Van Den Neste, Jean‐Philippe Defour, Étienne Danse, Jean Cyr Yombi,
Tópico(s)Parvovirus B19 Infection Studies
ResumoHemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder characterized by hyperimmune response. The mortality is high despite progress being made in the diagnosis and treatment of the disease.
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