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Published on: March 30, 2018
Kawasaki disease with a concomitant primary Epstein - Barr virus infection
Nataly Rosenfeld1, Diana Tasher2, Adi Ovadia2
1Department of Paediatrics, Edith Wolfson Medical Center, Halochamim 62, Holon, Israel. natalyrosenfeld@gmail.com.
Insights
Kawasaki disease (KD) is a leading cause of acquired heart disease in children. This case report details a child with KD and acute Epstein-Barr virus (EBV) infection, suggesting a potential role for EBV in KD development.
Area of Science:
- Pediatric Cardiology
- Infectious Diseases
- Immunology
Background:
- Kawasaki disease (KD) is the primary cause of acquired heart disease in children.
- The etiology of KD remains unknown, with infectious agents triggering abnormal immune responses suspected.
- Epstein-Barr virus (EBV) is under investigation due to its immunomodulatory effects.
Observation:
- A 19-month-old boy presented with classic KD symptoms, including fever, rash, conjunctivitis, and swollen extremities.
- Initial treatment with IVIG and aspirin was ineffective, requiring a second IVIG course.
- Readmission revealed leukocytosis with atypical lymphocytes and elevated liver enzymes, alongside positive EBV serology and PCR.
Findings:
- The patient was diagnosed with Kawasaki disease and confirmed primary Epstein-Barr virus infection.
- This is the first reported case in a Western country of KD with acute EBV infection confirmed by PCR.
- The patient showed a favorable response after a second IVIG course.
Implications:
- This case supports the hypothesis that EBV may play a role in the pathogenesis of Kawasaki disease.
- Further research is warranted to explore the link between EBV and KD.
- Understanding potential infectious triggers can inform KD diagnosis and treatment strategies.
Background:
Kwasaki disease (KD) is the leading cause of acquired heart disease in children in most developed countries. The cause of KD remains unknown. The presumed theory is that KD occurs due to one or more infectious agents who evoke an abnormal immunological response in susceptible individuals. Epstein - Barr virus (EBV) infection has been considered as a suspected causative agent because of the potential effect on the immune system.
Case Presentation:
A previously healthy 19 month old boy presented with a 6 day history of fever accompanied by a diffuse macular erythematous rash that appeared 1 day after. The physical examination on admission revealed bilateral non-suppurative conjunctivitis, dry fissured and injected lips without "strawberry" tongue, diffuse macular rash on the trunk, face and limbs, swelling of the hands and feet, and right cervical lymphadenopathy (2 cm in diameter). Following fulfillment of all the clinical criteria, the diagnosis of KD was made and treatment with IVIG 2 g/Kg was administered along with oral aspirin (80 mg/ kg/day). However, despite the treatment, he remained febrile for an additional 2 days with persistent clinical manifestations. Therefore, he received a second 2 g/kg IVIG course with a favorable response. On the 14th day of illness the patient became febrile again and was readmitted. Blood examinations revealed remarkable leukocytosis up to 35.7 X 109/L with 87.3% lymphocytes and the blood smear revealed atypical lymphocytes and monocytes. The liver enzymes were elevated. The serology for infectious mononucleosis from his first admission revealed: IgM CMV (+), IgG CMV (-); IgM VCA EBV (+) IgG VCA EBV (-), IgG EBNA (-). To confirm infectious mononucleosis following the administration of 2 doses of IVIG, serum EBV PCR was performed and was positive (1.6X 103 cp/ml).
Conclusions:
We describe here a case of KD with a concomitant primary EBV infection. To the best of our knowledge, this is the first case in western country that describes KD with acute EBV infection as confirmed by PCR. The case we described stands as a contribution in favor of the possible role of EBV in the development of KD.
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