2011
DOI: 10.4103/0377-4929.85105
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Hemophagocytic syndrome associated with Plasmodium falciparum infection

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.

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Cited by 14 publications
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“…Although severe malaria per se can cause cytopaenia, HLH was considered more likely in this patient because the cytopaenia developed during the resolution phase of malaria and was associated with hypofibrinogenaemia, hyperferritinaemia, hypertriglyceridaemia and a high index of haemophagocytosis in the bone marrow. HLH has been previously reported with both Mycoplasma and malaria [7, 8]. Although other cytokine markers were not tested due to unavailability, this patient fulfilled the standard diagnostic criteria for HLH.…”
Section: Discussionmentioning
confidence: 81%
“…Although severe malaria per se can cause cytopaenia, HLH was considered more likely in this patient because the cytopaenia developed during the resolution phase of malaria and was associated with hypofibrinogenaemia, hyperferritinaemia, hypertriglyceridaemia and a high index of haemophagocytosis in the bone marrow. HLH has been previously reported with both Mycoplasma and malaria [7, 8]. Although other cytokine markers were not tested due to unavailability, this patient fulfilled the standard diagnostic criteria for HLH.…”
Section: Discussionmentioning
confidence: 81%
“…[ 6 ] Several studies showed that malaria-HLH patients treated by anti-malaria drugs only without the use of any immunosuppressive drug and other steroids. [ 7 8 ]…”
Section: Discussionmentioning
confidence: 99%