Hemophagocytic lymphohistiocytosis secondary to visceral leishmaniasis: A case report of a rare complication of visceral leishmaniasis

Hemophagocytic lymphohistiocytosis (HLH) is a rare, potentially life-threatening clinical syndrome characterized by hyperactivation of inflammatory mediators and harmful end-organ damage. Visceral leishmaniasis (VL)-induced HLH is a rare disease with significant diagnostic and management implication...

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Hlavní autoři:	Telila K. Belisa, Asteway M. Haile, Getinet B. Mesfin, Biruk T. Mengistie, Chernet T. Mengistie, Bezawit M. Haile
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Elsevier 2024-01-01
Edice:	IDCases
Témata:	Hemophagocytic Lymphohistiocytosis(HLH) Visceral Leishmaniasis(VL) Toddler Case report
On-line přístup:	http://www.sciencedirect.com/science/article/pii/S2214250924001355
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