Secondary hemophagocytic lymphohistiocytosis induced by malaria infection in a child with Langerhans cell histiocytosis
PEDIATRIC HEMATOLOGY AND ONCOLOGY, vol.21, no.3, pp.267-272, 2004 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 21 Issue: 3
- Publication Date: 2004
- Doi Number: 10.1080/08880010490277060
- Journal Name: PEDIATRIC HEMATOLOGY AND ONCOLOGY
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Page Numbers: pp.267-272
- Keywords: Langerhans cell histiocytosis, malaria infection, secondary hemophagocytic lymphohistiocytosis, virus-associated hemophagocytic syndrome, MIMICKING MALIGNANT HISTIOCYTOSIS, EPSTEIN-BARR VIRUS, FALCIPARUM-MALARIA
- Istanbul University Affiliated: Yes
Abstract
Since the first description of infection-associated hemophagocytosis (IAHS), the list of precipitating infectious agents causing hemophagocytic syndrome has grown. A lymphohistiocytic proliferation with hemophagocytosis may develop as a result of macrophage activation, viral or bacterial infection, parasitic infestations, or malignancy. The authors report on a 3-year-old boy with Langerhans cell histiocytosis (LCH), who developed IAHS during malaria infection. Hemophagocytic syndromes may complicate the course of LCH and cause diagnostic problems. Malaria is one of many infections that can precipitate secondary hemophagocytic lymphohistiocytosis.