# Hemophagocytic Lymphohistiocytosis Triggered by Acute Dengue Infection in a Young Adult: A Case Report From the United Arab Emirates

**Authors:** Niyas Khalid Ottu Para, Hala Oweis, Seema Rab

PMC · DOI: 10.7759/cureus.103135 · Cureus · 2026-02-06

## TL;DR

A young man in the UAE developed a rare, severe immune condition called HLH after a dengue infection, highlighting the importance of early diagnosis and treatment.

## Contribution

This case report highlights the rare but critical association between acute dengue infection and secondary HLH in a non-endemic region.

## Key findings

- A 22-year-old male with acute dengue developed secondary HLH, marked by extreme hyperferritinemia and hypofibrinogenemia.
- Early corticosteroid treatment led to rapid clinical and biochemical improvement, preventing severe complications.
- The case emphasizes the need for high suspicion of HLH in dengue patients with persistent fever and abnormal inflammatory markers.

## Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening hyperinflammatory syndrome characterized by uncontrolled immune activation and cytokine storm. Dengue, a flavivirus transmitted by Aedes mosquitoes, is usually self-limiting but may rarely trigger secondary HLH. Persistent fever accompanied by cytopenias, extreme hyperferritinemia, transaminitis, and hypofibrinogenemia should raise suspicion for this diagnosis. Although dengue is not endemic to the United Arab Emirates, a significant outbreak followed unprecedented rainfall and flooding in April 2024, resulting in a surge in imported and locally acquired cases and posing diagnostic challenges for hyperinflammatory conditions such as HLH. We report the case of a 22-year-old male admitted with acute dengue infection complicated by secondary HLH, diagnosed based on extreme hyperferritinemia, bicytopenia, marked transaminitis, and hypofibrinogenemia despite normal triglyceride levels. Early recognition and prompt initiation of corticosteroid therapy led to rapid clinical and biochemical improvement, preventing progression to a full-blown cytokine storm and the need for intensive care admission. This case underscores the importance of maintaining a high index of suspicion for HLH in dengue patients presenting with persistent fever and disproportionate inflammatory markers, particularly in young adults, even in non-endemic regions.

## Linked entities

- **Diseases:** Hemophagocytic Lymphohistiocytosis (MONDO:0015540), Dengue (MONDO:0005502), cytokine storm (MONDO:0600008)
- **Species:** Aedes (taxon 7158)

## Full-text entities

- **Diseases:** cytokine storm (MESH:D000080424), cytopenias (MESH:D006402), Dengue Infection (MESH:D003715), hypofibrinogenemia (MESH:D000347), fever (MESH:D005334), hyperinflammatory syndrome (MESH:D013577), HLH (MESH:D051359), inflammatory (MESH:D007249), hyperferritinemia (MESH:D000085583)
- **Chemicals:** triglyceride (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12972619/full.md

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Source: https://tomesphere.com/paper/PMC12972619