The first demonstrated case of human babesiosis in the world was repor
ted in Europe, in 1957. Since then, a further 28 babesial infections i
n man have been reported in Europe. Most (83%) of the infections were
in asplenic individuals and most (76%) were with Babesia divergens, a
cattle parasite. Parasitaemias varied from 1%-80% of red blood cells.
The usual clinical manifestations of severe B. divergens infection wer
e severe intravascular haemolysis with haemoglobinuria. The most effic
ient treatment consisted of a massive blood-exchange transfusion, foll
owed immediately by c:hemotherapy with clindamycin. Hundreds of cases
of human infection with Babesia spp. have been reported in the U.S.A.
Most cases were infected by ticks carrying the rodent parasite B. micr
oti, bur other emerging Babesia spp. (currently known as WA(1), CA(1)
and MO1) are increasingly involved. Several cases were the result of b
lood transfusion. In terms of clinical manifestations, human infection
s with B. microti varied widely, from asymptomatic infection to a seve
re, rapidly fatal disease. Parasitaemia ranged between < 1% and 85%. T
he splenectomized, the elderly, the immunocompromised and HIV-infected
patients were predisposed to severe infection. Infections with B. mic
roti often remained subclinical or asymptomatic and were only detected
through serological surveys. The currently recommended treatment of s
ymptomatic cases is quinine plus clindamycin. A few other cases of hum
an babesial infection have been described in China, Egypt, Mexico, Sou
th Africa and Taiwan.