Hemophagocytic lymphohistiocytosis secondary to visceral leishmaniasis: A case report of a rare complication of visceral leishmaniasis.
Case report
Hemophagocytic Lymphohistiocytosis(HLH)
Toddler
Visceral Leishmaniasis(VL)
Journal
IDCases
ISSN: 2214-2509
Titre abrégé: IDCases
Pays: Netherlands
ID NLM: 101634540
Informations de publication
Date de publication:
2024
2024
Historique:
received:
29
06
2024
revised:
16
07
2024
accepted:
10
08
2024
medline:
3
9
2024
pubmed:
3
9
2024
entrez:
3
9
2024
Statut:
epublish
Résumé
Hemophagocytic lymphohistiocytosis (HLH) is a rare, potentially life-threatening clinical syndrome characterized by hyperactivation of inflammatory mediators and harmful end-organ damage
Identifiants
pubmed: 39224873
doi: 10.1016/j.idcr.2024.e02059
pii: S2214-2509(24)00135-5
pmc: PMC11367473
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Pagination
e02059Informations de copyright
© 2024 The Authors.
Déclaration de conflit d'intérêts
The authors declare that they have no known competing financial interests or personal relationships that could have influenced the work reported in this paper.