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Multisystem inflammatory syndrome in children (MIS-C) of a toddler initially presenting with fever and pyuria
Kinyui Alice Lo1, Lee Gan Goh2,3, Rajeev Ramachandran4,5
1Department of Family Medicine, National University Health System, Singapore lokinyui@gmail.com.
Insights
This case study details multisystem inflammatory syndrome in children (MIS-C) in a young East Asian toddler, presenting uniquely with pyuria. Early diagnosis and treatment are crucial, though coronary abnormalities may persist.
Area of Science:
- Pediatrics
- Infectious Diseases
- Cardiology
Background:
- Multisystem inflammatory syndrome in children (MIS-C) is a rare but serious condition following SARS-CoV-2 infection.
- Early recognition is vital for timely intervention and management of potential complications.
Observation:
- A young East Asian toddler presented with fever, pyuria, conjunctivitis, and extremity changes 5 weeks post-COVID-19 recovery.
- Initial symptoms mimicked a urinary tract infection, delaying MIS-C diagnosis.
Findings:
- Laboratory results revealed elevated inflammatory markers, thrombocytopenia, and markedly elevated NT-proBNP.
- Despite prompt inpatient treatment, mild coronary abnormalities were noted 9 months post-discharge.
Implications:
- This case highlights the diverse presentations of MIS-C, including pyuria, and its occurrence in specific demographics.
- Emphasizes the need for heightened clinical suspicion for MIS-C in children with post-viral febrile illnesses, even with atypical initial symptoms.
Abstract:
We report a case of multisystem inflammatory syndrome in children (MIS-C) in an East Asian toddler. He presented with a 2-day history of fever and pyuria, 5 weeks before that he had recovered from COVID-19. He was initially treated as urinary tract infection. On day 5 of fever, he was noted to have bilateral non-suppurative limbus-sparing conjunctivitis, red and cracked lips and erythematous extremities. Investigations showed raised inflammatory markers (C-reactive protein and erythrocyte sedimentation rate), thrombocytopenia and a markedly elevated NT-proBNP. He received prompt and appropriate treatment inpatient; however, he still had mild coronary abnormalities at 9 months postdischarge. The aim of this paper is to describe the initial presentation and progress of a case of MIS-C. The unique features of this case are his initial presentation of pyuria and notably, his demography (young age, East Asian) which is more typical of Kawasaki disease than MIS-C.
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