|Frey-Wettstein M, Maier A, Markwalder K, Münch U.||
Swiss Med Wkly 2001;131:320
|Letter to the editor|
|On July 29 th, 1999 a 70-year-old
male patient was operated on at the University Hospital, Zurich for coronary
artery disease and aortic aneurysm. One month later on August 25 th a second
operation was necessary. On both occasions he received a total of 26 units
of blood-products, 16 units of packed cells and 10 of fresh frozen plasma.
Two weeks after the second operation there was an unexplained deterioration in his general wellbeing. He developed a fever and his laboratory tests showed signs of acute infection. 22 days after re-operation the fever reached 40 °C. The next day the laboratory reported the presence of plasmodia in blood smears. Retrospectively plasmodia could be found in a blood smear prepared 3 days earlier. The diagnosis of falciparum malaria was established. In spite of appropriate antimalarial treatment the multimorbid patient died 3 days later due to circulatory and multiorgan failure.
As the patient had not travelled to tropical regions in the recent past, alternative explanations for the malarial infection were evaluated. Airport malaria was considered as a possibility, as the patient lived close to the International Airport in Zurich, where such cases have been observed previously. A retrospective analysis of the transfused red cell units was initiated to exclude transfusion malaria. 16 donors of red cell concentrates were recalled for a malaria falciparum IFTA antibody test. One of the donors showed a malaria antibody titer of >160 (normal value <40) 3 months after the index donation, when repeated of 640. At this time no malarial parasites could be found in the blood smears of this donor. 3 weeks later a control revealed low numbers of P. falciparum gametozytes. A further month later (without treatment) the blood smears showed asexual parasitaemia and P. falciparum PCR was positive. PCR analysis confirmed the identical species of P. falciparum in donor and recipient, thus proving transfusion associated aetiology of the patient’s disease. A serothek specimen of a previous donation of the donor was available for malaria screening. Similar to the index donation it proved to be malaria falciparum antibody positive. Because of the benign course of the malaria infection the donor was treated with a course of Malarone.
The donor n question is a 30-year-old native from Cameroon, his parents coming from Cameroon and Guadeloupe respectively. He left Cameroon 10 years ago, was last there for a visit 6 years ago, and has since not been to any tropical area endemic for malaria. Before moving to Switzerland he lived in France for 8 or 9 years, close to International Airport Paris-Roissy. He has always been in good health and does not recall having had any fever attacks n the last few years. He remembers having had malaria at the age of 15, when still living in Cameroon. He has donated blood twice since moving to Switzerland. The recipient of the first donation is in good health and has been tested malaria falciparum antibody negative.
The origin of the malaria infection of the index donor is unclear. It must have been acquired before his first blood donation in Switzerland. Acquisition during his last visit in Cameroon 6 years ago appears unlikely as chronic asymptomatic malaria falciparum infection of several years of duration is unlikely [1,2]. We assume that the donor acquired his malaria more recently, most likely during his stay near Paris-Roissy Airport. Likewise baggage malaria (importation of malaria infected mosquitos in the luggage of travellers returning from vacation in tropical areas)  must be considered.
Zurich Blood Transfusion Service SRC, Zurich, Switzerland
Department of Medicine, District Hospital, Bülach, Switzerland
Private Practice for Tropical Medicine, Zurich, Switzerland
Copyright © 2001 EMH Swiss Medical Publishers Ltd.