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Concurrent Coxsackievirus A6 Infection and Kawasaki Disease: A Case Report
Jiratchaya Puenpa1, Noree Saelim2, Nasamon Wanlapakorn1
1Center of Excellence in Clinical Virology, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
Insights
Coxsackievirus A6 (CVA6) infection may trigger Kawasaki disease (KD) in children. This case report details a CVA6-associated herpangina leading to KD diagnosis, emphasizing timely recognition during enterovirus seasons.
Area of Science:
- Pediatrics
- Infectious Diseases
- Virology
Background:
- Kawasaki disease (KD) is a critical pediatric vasculitis affecting coronary arteries.
- Coxsackievirus A6 (CVA6) is increasingly linked to atypical hand, foot, and mouth disease (HFMD).
- Investigating potential viral triggers for KD is crucial for understanding its pathogenesis.
Observation:
- An 18-month-old boy presented with fever, sore throat, and ulcerative lesions, initially diagnosed as herpangina.
- The patient subsequently developed classic KD symptoms, including conjunctivitis and rash, with elevated inflammatory markers.
- Throat swab confirmed CVA6 infection, with phylogenetic analysis linking the strain to recent Chinese isolates.
Findings:
- This case suggests a potential association between CVA6-induced herpangina and the development of Kawasaki disease.
- The identified CVA6 strain exhibited high sequence homology with contemporary strains, indicating a possible recent introduction or circulation.
Implications:
- CVA6 may serve as a trigger for KD in genetically susceptible children.
- Increased clinical awareness is needed for prompt KD diagnosis and management during enterovirus outbreaks.
- Early identification and treatment of KD can mitigate severe cardiovascular complications in children.
Abstract:
Background and Clinical Significance: Kawasaki disease (KD) is an acute febrile vasculitis that primarily affects children and is associated with systemic inflammation, particularly in the coronary arteries. Coxsackievirus A6 (CVA6) has emerged as a significant agent in atypical presentations of hand, foot, and mouth disease (HFMD), raising the possibility of its involvement in KD. Case Presentation: This report presents the case of an 18-month-old Thai boy admitted with symptoms of high fever, sore throat, and ulcerative lesions, initially diagnosed with herpangina. As his condition progressed, additional KD symptoms developed, including conjunctival injection, rash, and elevated inflammatory markers, fulfilling the diagnostic criteria for KD. Notably, throat swab analysis confirmed CVA6 as the causative agent. Phylogenetic analysis revealed that the CVA6 strain closely aligned with Chinese strains from 2023, showing a high nucleotide sequence homology of 98.4%. Conclusions: In conclusion, this case highlights a possible association between CVA6-associated herpangina and KD, suggesting that CVA6 infection may act as a trigger for KD in genetically susceptible children. These findings highlight the need for increased awareness among healthcare providers to promptly identify and manage Kawasaki Disease during peak enterovirus seasons, reducing its impact on children.
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