Hemophagocytic lymphohistiocytosis in adults: An under recognized entity

Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of severe immune activation with macrophage and T-cell infiltration resulting in, multi organ damage. HLH may be primary or secondary in etiology. A high index of suspicion is essential for early diagnosis and treatment. Diagnostic criteria need...

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Bibliografiske detaljer
Udgivet i:BBA Clin
Main Authors: Shah, Abdul Rashid, Muzzafar, Tariq, Assi, Rita, Schellingerhout, Dawid, Estrov, Zeev, Tamamyan, Gevorg, Kantarjian, Hagop, Daver, Naval
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 2016
Fag:
Regular Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5219626/
https://ncbi.nlm.nih.gov/pubmed/28070498
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbacli.2016.12.002
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