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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Bibliographic Details
Main Authors: Kartik Goel, Reshma Prakash, Harsh Kansagara, Shailesh Kumar, Rupesh Yadav
Format: Article
Language:English
Published: Towarzystwo Pomocy Doraźnej 2025-03-01
Series:Critical Care Innovations
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Online Access:https://www.irdim.net/cci/8(1)51-56.html
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