Adult secondary hemophagocytic lymphohistiocytosis
Abstract Background Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of excessive inflammation and tissue destruction due to abnormal immune activation. HLH carries a very high mortality, and while delays in patients’ presentation to hospital, time to suspicion of HLH, investigation, and initi...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2020-11-01
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Series: | eJHaem |
Subjects: | |
Online Access: | https://doi.org/10.1002/jha2.113 |