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Autor:
Telila K. Belisa, Asteway M. Haile, Getinet B. Mesfin, Biruk T. Mengistie, Chernet T. Mengistie, Bezawit M. Haile
Publikováno v:
IDCases, Vol 37, Iss , Pp e02059- (2024)
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
Externí odkaz:
https://doaj.org/article/e5d09bdca4eb43e28e17423e1d898feb
