Babesia infection in Italy.
Babesia infection in Italy.
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DOI:
10.1016/s1473-3099(04)00970-3
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发表时间:
2004-04-01
期刊:
影响因子:
--
通讯作者:
Gherlinzoni, Filippo
中科院分区:
文献类型:
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作者:
Piccaluga, Pier Paolo;Poletti, Giovanni;Gherlinzoni, Filippo
Our patient is a 55-year-old man who had undergone to splenectomy for Hodgkin’s disease in 1980. He started chemotherapy for a diffuse large B-cell lymphoma in 1998. During chemotherapy, the patient presented with fever (39 C), confusion, severe anaemia, thrombocytopenia, haemoglobinuria, and lactate dehydrogenase, creatinine, and bilirubine elevation. He had no history of tick bites, foreign travel, or transfusion. Babesiosis was diagnosed by observing parasitic inclusions in erythrocytes on peripheralblood smears (figure, presence of intraerythrocytic protozoa suggestive for babesia infection is outlined). Antibody titre against Babesia divergens was weakly positive. Specific therapy with clindamicine (600 mg thrice daily intravenously) and quinine sulphate (650 mg thrice daily orally) was administered for 15 days. Fever resolved after 3 days of therapy; parasites disappeared from blood-smears after 6 days. The infection never recurred. Babesiosis is a tick-borne zoonosis caused by intraerythrocytic protozoa of the genus Babesia. Since the first case was described in 1956, hundreds of cases of human babesiosis have been reported in the USA, about 30 in Europe, and only a few cases elsewhere. Babesia microti is the species most often responsible for the cases reported in USA, whereas B divergens is most frequently found in European cases. Other species have been identified in USA and described by molecular characterisation, including WA1, CA1, and MO1 types. We believe our patient was the first case of babesiosis in Italy. The molecular characterisation (performed at the Centers for Disease Control and Prevention, Atlanta, USA) showed that the parasite, although related to B divergens, was a previously unrecognised babesia organism, defined as EU1 (European Union 1).