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Published on: May 16, 2013
Hemophagocytic syndrome associated with Plasmodium falciparum infection
P N Vinoth1, K Abilash Thomas, S Muthamil Selvan
1Department of Pediatrics, Sri Ramachandra Medical College, Chennai, India.
Insights
Malaria rarely causes hemophagocytic syndrome (HPS). This case shows an infant with HPS due to Plasmodium falciparum malaria, recovering quickly with antimalarial treatment.
Area of Science:
- Pediatrics
- Infectious Diseases
- Hematology
Background:
- Hemophagocytic syndrome (HPS) is a severe, life-threatening condition.
- HPS is often linked to infections, cancers, or autoimmune disorders.
- Malaria is an uncommon cause of HPS.
Observation:
- An 11-month-old infant presented with fever, enlarged liver and spleen, and low blood counts.
- Laboratory tests revealed high ferritin and triglycerides, with hemophagocytosis in bone marrow.
- Plasmodium falciparum gametocytes were detected in the bone marrow.
Findings:
- The infant's presentation was consistent with hemophagocytic syndrome.
- The underlying cause of HPS was identified as Plasmodium falciparum malaria.
- Bone marrow examination confirmed the presence of malaria parasites.
Implications:
- This case highlights malaria as a potential, albeit rare, cause of HPS in infants.
- Early diagnosis and prompt antimalarial treatment are crucial for favorable outcomes.
- Further research may elucidate the mechanisms linking malaria to HPS.
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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