Abstract
Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal hyper-inflammatory disease induced by aberrant immune activation and subsequent proliferation of macrophages, histiocytes and T-helper cells. In this abstract we present a case of HLH, which relapsed twice despite ongoing treatment, and we hypothesize on possible causes and mechanisms...
Original language | English |
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Pages (from-to) | 24-26 |
Number of pages | 3 |
Journal | Blood |
Volume | 136 |
Issue number | Supplement 1 |
DOIs | |
Publication status | Published - 5 Nov 2020 |
Externally published | Yes |
Keywords
- Hemophagocytic Lymphohistiocytosis
- hyper-inflammatory disease
- aberrant immune activation
- Myeloid Gene Mutation