Hemophagocytic lymphohistiocytosis secondary to T-cell/histiocyte-rich large B-cell lymphoma

Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening clinical syndrome characterized by dysregulation of the immune system. Impaired function of cytotoxic T cells and natural killer cells is often seen, and T-cell malignancies represent most cases of lymphoma-associated HLH. HLH associated...

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Bibliografiske detaljer
Main Authors: Devitt, Katherine, Cerny, Jan, Switzer, Bradley, Ramanathan, Muthalagu, Nath, Rajneesh, Yu, Hongbo, Woda, Bruce A., Chen, Benjamin J.
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 2014
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4062756/
https://ncbi.nlm.nih.gov/pubmed/24955327
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.lrr.2014.05.004
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