Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum Malaria
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. Afte...
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2014-06-01
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Online Access: | http://ejcrim.com/index.php/EJCRIM/article/view/73 |
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doaj-3ea3ea847a4b4e378ad2119eb2f9d6902020-11-25T00:30:08ZengSMC MEDIA SRLEuropean Journal of Case Reports in Internal Medicine2284-25942014-06-011110.12890/2014_00007337Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum MalariaRembert Mertens0Sabine D Allard1Lucie Seyler2Kristin Jochmans3Patrick Lacor4Universitair Ziekenhuis BrusselUniversitair Ziekenhuis BrusselUniversitair Ziekenhuis BrusselUniversitair Ziekenhuis BrusselUniversitair Ziekenhuis BrusselObjectives: 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.http://ejcrim.com/index.php/EJCRIM/article/view/73Plasmodium falciparum, hemophagocytic lymphohistiocytosis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rembert Mertens Sabine D Allard Lucie Seyler Kristin Jochmans Patrick Lacor |
spellingShingle |
Rembert Mertens Sabine D Allard Lucie Seyler Kristin Jochmans Patrick Lacor Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum Malaria European Journal of Case Reports in Internal Medicine Plasmodium falciparum, hemophagocytic lymphohistiocytosis |
author_facet |
Rembert Mertens Sabine D Allard Lucie Seyler Kristin Jochmans Patrick Lacor |
author_sort |
Rembert Mertens |
title |
Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum Malaria |
title_short |
Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum Malaria |
title_full |
Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum Malaria |
title_fullStr |
Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum Malaria |
title_full_unstemmed |
Haemophagocytic Syndrome in a 19-Year-Old Male with Plasmodium falciparum Malaria |
title_sort |
haemophagocytic syndrome in a 19-year-old male with plasmodium falciparum malaria |
publisher |
SMC MEDIA SRL |
series |
European Journal of Case Reports in Internal Medicine |
issn |
2284-2594 |
publishDate |
2014-06-01 |
description |
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. |
topic |
Plasmodium falciparum, hemophagocytic lymphohistiocytosis |
url |
http://ejcrim.com/index.php/EJCRIM/article/view/73 |
work_keys_str_mv |
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