Nederlands Tijdschrift voor Geneeskunde
Volume 160, Issue 50, 2016
Splenomegaly in an Eritrean refugee: The hyper-reactive malaria splenomegaly syndrome [Splenomegalie bij een Eritrese vluchteling: HET HYPERREACTIEF-MALARIA-SPLENOMEGALIESYNDROOM] (Article)
Cruijsen M.M. ,
Reuling I.J. ,
Keuter M. ,
Sauerwein R.W. ,
Van Der Ven A.J. ,
De Mast Q.*
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a
Radboudumc, Nijmegen, Netherlands
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b
Radboudumc, Nijmegen, Netherlands
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c
Radboudumc, Nijmegen, Netherlands
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d
Radboudumc, Nijmegen, Netherlands
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e
Radboudumc, Nijmegen, Netherlands
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f
Radboudumc, Nijmegen, Netherlands
Abstract
Background Hyper-reactive malaria splenomegaly (HMS) is a rare and potentially severe complication of malaria. It is likely that the incidence of patients with HMS will rise in the Netherlands due to the recent increase in asylum-seekers from Sub-Saharan Africa. It can be difficult to diagnose this disease, as this case shows. Case description A 31-year-old male from Eritrea was admitted with fever and dyspnea, caused by an influenza A-infection. The patient also presented with cachexia, pronounced hepatosplenomegaly and pancytopenia. Microscopic diagnostic analysis for malaria was negative. HMS was eventually diagnosed through high-sensitivity qPCR for malaria, which showed the presence of a very low level of Plasmodium falciparum parasitemia; furthermore, IgM levels were high and malaria serology was strongly positive. Conclusion HMS should be considered in patients from malaria-endemic areas presenting with splenomegaly and pancytopenia. Because standard diagnostics for malaria are often negative in this population, malaria serology and sensitive qPCR play an important diagnostic role.
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Link
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85006300298&partnerID=40&md5=4dfe4760b5cfa35728099b5e081ea1d6
ISSN: 00282162
Original Language: Dutch