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Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum Malaria
oleh: Rembert Mertens, Sabine D Allard, Lucie Seyler, Kristin Jochmans, Patrick Lacor
Format: | Article |
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Diterbitkan: | SMC MEDIA SRL 2014-06-01 |
Deskripsi
Objectives: Infectious agents triggering haemophagocytic lymphohistiocytosis (HLH) primarily involve the herpes virus group. We report a case of HLH precipitated by Plasmodium falciparum. Materials and methods: Clinical and laboratory findings in a patient presenting with fever were collected. After confirmation of acute malaria, anti-malarial treatment was administered. Results: Despite initial favourable evolution, the patient developed fever again together with a worsening of the haematological parameters and increased ferritin levels. A bone marrow biopsy confirmed the diagnosis of HLH. Conclusion: This case illustrates that HLH should be considered in the differential diagnosis of acute malaria in patients with persisting fever and pancytopenia.