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Indian J Pathol Microbiol ; 2011 Jul-Sept 54(3): 594-596
Article in English | IMSEAR | ID: sea-142053

ABSTRACT

Hemophagocytic syndrome (HPS) has been associated with infections, hematological malignancies and autoimmune conditions. Malaria is rarely reported to cause HPS. We report a case of an 11-month-old infant with fever, hepatosplenomegaly, pancytopenia, high serum ferritin, hypertriglyceridemia, and bone marrow hemophagocytosis, consistent with hemophagocytic syndrome. Gametocytes of plasmodium falciparum were identified on bone marrow aspiration. Rapid recovery was observed after treatment with antimalarials.


Subject(s)
Antimalarials/administration & dosage , Bone Marrow/parasitology , Bone Marrow/pathology , Humans , Infant , Lymphohistiocytosis, Hemophagocytic/diagnosis , Lymphohistiocytosis, Hemophagocytic/etiology , Malaria, Falciparum/complications , Malaria, Falciparum/drug therapy , Malaria, Falciparum/pathology , Male , Microscopy , Plasmodium falciparum/cytology , Treatment Outcome
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