Hemophagocytic lymphohistiocytosis in children with visceral leishmaniasis. [artículo]
Por: Blázquez Gamero, Daniel [Pediatría]
| Domínguez Pinilla, Nerea [Pediatría] | Negreira Cepeda, Sagrario [Pediatría] | Ruiz Contreras, Jesús [Pediatría].
Colaborador(es): Servicio de Pediatría-Neonatología.
Tipo de material: 
ArtículoEditor: The Pediatric infectious disease journal, 2015Descripción: 34(6):667-9.Recursos en línea: Solicitar documento Resumen: Acquired hemophagocytic lymphohistiocitosis (HLH) syndrome can be a complication of visceral leishmaniasis (VL). A multicenter prospective study was conducted to determine the frequency of HLH syndrome in children with VL. Twenty-four children with VL were identified, and 10 (41%) developed HLH syndrome. VL should be ruled out in all children with HLH criteria living in or coming from endemic areas.
| Tipo de ítem | Ubicación actual | Signatura | Estado | Fecha de vencimiento |
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Artículo
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P17053 (Navegar estantería) | Disponible |
Formato Vancouver:
Blázquez Gamero D, Domínguez Pinilla N, Chicharro C, Negreira S, Galán P, Pérez Gorricho B et al; Madrid Leishmaniasis Study Group. Hemophagocytic lymphohistiocytosis in children with visceral leishmaniasis. Pediatr Infect Dis J. 2015 Jun;34(6):667-9.
PMID: 25970110
Contiene 19 referencias
Acquired hemophagocytic lymphohistiocitosis (HLH) syndrome can be a complication of visceral leishmaniasis (VL). A multicenter prospective study was conducted to determine the frequency of HLH syndrome in children with VL. Twenty-four children with VL were identified, and 10 (41%) developed HLH syndrome. VL should be ruled out in all children with HLH criteria living in or coming from endemic areas.
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