The study was approved by the patient and the Ethics Committee of Kunming General Hospital of Chengdu Military Region. Severe parasitemia was observed by microscopic examination of the erythrocytes in the bone marrow fluid with Wright stain (
Figure 1 A, Nikon, E200). The morphology of
Babesia was subsequently assessed by thin blood smears stained with Giemsa (
Figure 1 B). For further identification of
Babesia infection, blood samples were fixed, dehydrated, thin sectioned, and stained for transmission electron microscopy (TEM, Hitachi, H-9500, Japan) according to a previous study (
5). Vacuolization of the host cytoplasm was observed by TEM (
Figure 1 C, black arrow). To distinguish between
Plasmodium falciparum and
Babesia infection, indirect fluorescent antibody test (IFA) was performed using the
Babesia microti IgG IFA kit (BMG-120, Gentaur, Belgium, at 1:256 dilutions) as the antigen to detect antibodies in the blood smears (
Figure 1 D, black arrow). The detection of
Babesia specific antibody by IFA is the most prominent tool for diagnosis, with specificity of 100% in patients with other tick borne diseases or those not exposed to the parasite (
6).