A case report of a hemophagocytic lymphohistiocytosis secondary to an extranodal NK T cell lymphoma
Hemophagocytic Lymphohistiocytosis HLH is a rare, lifethreatening hyperinflammatory syndrome resulting from inappropriate and dysregulated activation of NK cells, CD8 cytotoxic Tcells, and macrophages.
Publication Details
- Journal
- Open Journal of Clinical and Medical Images
- Published
- 2025-03-27
- DOI
- https://doi.org/10.52768/2833-2725/1201
- Primary Topic
- Geochemistry and Geologic Mapping
- Type
- article
- Field-Weighted Citation Impact
- 0.00