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Ned Tijdschr Geneeskd ; 160: D444, 2016.
Artigo em Holandês | MEDLINE | ID: mdl-27848905

RESUMO

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.


Assuntos
Malária/diagnóstico , Malária/tratamento farmacológico , Refugiados , Esplenomegalia/diagnóstico , Esplenomegalia/tratamento farmacológico , Adulto , Eritreia , Hepatomegalia , Humanos , Malária/parasitologia , Masculino , Países Baixos , Esplenomegalia/parasitologia , Síndrome
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