Hemophagocytic lymphohistiocytosis in children with visceral leishmaniasis
- PMID: 25970110
- DOI: 10.1097/INF.0000000000000685
Hemophagocytic lymphohistiocytosis in children with visceral leishmaniasis
Abstract
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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