Scrub typhus complicating hemophagocytic lymphohistiocytosis: a case report.
Hemophagocytic lymphohistiocytosis (HLH) is a rare disorder characterised by uncontrolled activation of CD8+ T lymphocytes and macrophages, resulting in organ damage. While primary HLH is associated with genetic defects, secondary HLH can be triggered by infections, malignancies, or autoimmune disor...
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| Format: | Artigo |
| Sprache: | Inglês |
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Towarzystwo Pomocy Doraźnej
2025-03-01
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| Schriftenreihe: | Critical Care Innovations |
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| Online-Zugang: | https://www.irdim.net/cci/8(1)51-56.html |
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