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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Autors principals:	Telila K. Belisa, Asteway M. Haile, Getinet B. Mesfin, Biruk T. Mengistie, Chernet T. Mengistie, Bezawit M. Haile
Format:	Artigo
Idioma:	Inglês
Publicat:	Elsevier 2024-01-01
Col·lecció:	IDCases
Matèries:	Hemophagocytic Lymphohistiocytosis(HLH) Visceral Leishmaniasis(VL) Toddler Case report
Accés en línia:	http://www.sciencedirect.com/science/article/pii/S2214250924001355
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