Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum Malaria


Autoria(s): Mertens, Rembert; Allard, Sabine D.; Seyler, Lucie; Jochmans, Kristin; Lacor, Patrick
Data(s)

2014

Resumo

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.

Formato

text

Identificador

http://eprints.bice.rm.cnr.it/14959/1/73-652-4-PB.pdf

Mertens, Rembert and Allard, Sabine D. and Seyler, Lucie and Jochmans, Kristin and Lacor, Patrick (2014) Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum Malaria. European Journal of Case Reports in Internal Medicine, 1 (1). pp. 1-6. ISSN 2284-2594

Idioma(s)

en

Publicador

SMC media

Relação

http://eprints.bice.rm.cnr.it/14959/

http://ejcrim.com/index.php/EJCRIM/article/view/73

10.12890/2014_000073

Palavras-Chave #616 Malattie (classificare qui la Clinica medica, la medicina basata sull'evidenza, la Medicina interna, la Medicina sperimentale)
Tipo

Article

PeerReviewed