Prevalence of Epstein-Barr Virus Infection in Paediatric Patients with Adenotonsilar Enlargement
Omosule Ikeoluwa E1*, Gbujie Onyemuchechi Ibeneche1, Ibekwe Titus Sunday1 and BA Abimiku2
1University of Abuja Teaching Hospital Gwagwalada, Abuja, Nigeria
2Department of Pathology, University of Abuja Teaching Hospital Gwagwalada, Abuja, Nigeria
*Corresponding Author: Omosule Ikeoluwa E, University of Abuja Teaching Hospital Gwagwalada, Abuja, Nigeria.
Received:
May 14, 2024; Published: June 28, 2024
Abstract
Background: Epstein-Barr Virus (EBV) is a lymphotropic virus that is often responsible for various head and neck diseases. The virus typically remains dormant in lymphoid cells, including adenoid and tonsils, and can be reactivated later in life. Adenotonsilar enlargement is a common outpatient condition seen at the Ear Nose and Throat clinics. The common causes of adenotonsilar enlargement in children include allergy, exposure to chemical irritants and viral infections such as Epstein-Barr Virus. This virus has a trophic effect on nasopharyngeal tissues and has been implicated in the pathogenesis of diseases such as infectious mononucleosis, Burkitt’s lymphoma and nasopharyngeal neoplasms.
Objective: This study was designed to determine the prevalence of EBV among paediatric patient with adenotonsilar enlargement who had adenotonsillectomy and compare with controls
Methodology: This was a comparative cross- sectional study that was carried out at the ENT clinic of University of Abuja Teaching Hospital, Gwagwalada. Abuja, Nigeria. All eligible paediatric patients diagnosed with adenotonsilar enlargement were recruited by convenience sampling technique, following ethical approval and consent/assent. A structured questionnaire was used to obtain participant’s bio-data and clinical information from the parents or guardians of the participants. EBV status of the participants was evaluated serologically by Chemiluminescence Immuno Assay (CLIA) method. Data was analyzed using the Statistical Package for Social Sciences Version 24 and this was presented in prose, figures, tables and charts
Results: A total of 90 patients were recruited and grouped into the test (45) and control (45). They were age and sex matched p = 0.480 ꭓ2 = 0.498. M: F was 3.3:1, and 2.2:1 in control group The mean age group was 51.7 ± 5.4 months for the test group and 66.5 ± 5.6 months in the control group.
EBV IgG prevalence for the test group was 91.1% and 8.9% were EBV negative.
In the control group EBV IgG prevalence was 82% with 17% being EBV sero-negative. There was also a significant difference between the mean values of the EBV IgG in the test (29.6 ± 2.8) and control (12.4 ± 1.4) groups using the T-test analysis. T = 12.956, p = <0.001. Only two (2) patients in the test group tested positive to EBV IgM and IgG.
Conclusion: The results suggests that EBV is just as prevalent in our environment as it is in western climes, even though the titers were significantly higher among the test group.
Keywords: Prevalence of EBV; Adenotonsilar Enlargement; Chemiluminescence Immuno Assay Method; Epstein-Barr Virus; Volumetric Analysis
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