Blastocystis is an anaerobic and zoonotic micro-eukaryote with a global distribution, generally found in the large intestine of the human and a wide range of vertebrates (
10), as reported by Allexief more than 100 years ago (
15). Since the asymptomatic carriers of
Blastocystis spp. are common, its pathogenicity remained uncertain (
2). numerous digestive and non-digestive symptoms, such as diarrhea, abdominal pain, nausea, fatigue, constipation, flatulence, vomiting (
11), cutaneous disorders, and chronic or acute urticaria, are attributed to
Blastocystis infection (
16).
Blastocystis spp. can produce large quantities of proteases, hydrolases, and protease inhibitors, contributing to its pathophysiology. Instant serine protease can further result in stomachache, muscle contractions, and broad-spectrum pains (
12). Cysteine protease can also cleave human secretory immunoglobulin A (IgA) and promote mucosal adhesion of pathogens (
17). Many reports considered
Blastocystis spp. as opportunistic pathogens in immunocompromised patients; therefore, their clinical symptoms are more intense (
18). At the early stages of chemotherapy, a few cases colonized with
Blastocystis spp. are undetectable. The immune system of patients is compromised during chemotherapy, and consequently, the parasitic disease develops and diminishes the effect of chemo drugs, and accordingly, cancer progresses (
19). Among unicellular infections in immunocompromised individuals,
Blastocystis is the most common one. The findings of the present study showed that the prevalence of
Blastocystis infection was 21% (n = 11) in children with cancer, among which 11.5% had gastrointestinal symptoms; therefore, there was a significant relationship between
Blastocystis infection and gastrointestinal symptoms. According to Hafeez-Abdel et al., the prevalence of
Blastocystis infection in children with immunodeficiency was 12.1% in Egypt. Uysal et al., reported that 23. % of patients with common variable immune deficiency were infected with
Blastocystis spp. in Turkey (
20,
21). The data in the present study were also confirmed by Idris et al., reporting that 54.8% of 42 immunocompromised children with diarrhea were infected with
Blastocystis spp. in Indonesia (
22). Lack of significant differences in gender, age, and
Blastocystis spp. infection among the patients was another finding of the present study; however, Ozlem Years et al., obtained quite different results. They noted that the prevalence of
Blastocystis infection was higher in male patients than females, and interestingly, the rate of gastrointestinal symptoms was not significantly different between infected and non-infected cases (
23). Moe et al., found an age-related susceptibility to
Blastocystis infection in immunocompetent BALB/c mice. In the concerned investigation, juvenile mice were more susceptible than adult cases, and eight-week-old adult mice were resistant to
Blastocystis infection (
24). This difference might be related to various
Blastocystis strains, the issue needs molecular studies. During chemotherapy, the risk of parasitic infections is minimized due to particular conditions, including lifestyle, diet, and environment; therefore, it can be claimed that it is the opportunity for opportunistic pathogens to invade and cause clinical problems (
25). Fontanet believed that there was no significant difference in the prevalence of parasitic infections among people with and without immunodeficiency. On the other hand, in some studies, such as the one by Escobedo and Nunez, the prevalence of
Blastocystis infection was reported higher in immunocompromised patients compared with healthy individuals (
25). Under such circumstances, person-to-person was the main route of transmission. The limitation of the present study was the relatively small sample size.