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SARS-CoV-2-associated inflammatory multisystem disease in a 15-year-old boy
Cecília Ormay1, Beáta Onozó1, Réka Fitala1
11 Velkey László Gyermekegészségügyi Központ, Borsod-Abaúj-Zemplén Megyei Központi Kórház és Egyetemi Oktató Kórház, Miskolc, Szentpéteri kapu 72-76., 3525.
Paediatric inflammatory multisystem syndrome (PIMS) can occur in children after SARS-CoV-2 infection, presenting with shock and multiorgan failure. Antibody tests confirm prior infection, guiding intensive care and treatment for recovery.
Area of Science:
- Pediatric critical care medicine
- Infectious diseases
- Rheumatology
Background:
- Emergence of novel multisystem inflammatory syndromes in children following SARS-CoV-2 infection.
- Recognition of paediatric inflammatory multisystem syndrome (PIMS) as a distinct entity mimicking Kawasaki disease.
- Challenges in diagnosing PIMS due to negative viral RNA detection at presentation.
Observation:
- A 15-year-old male presented with high fever, rash, conjunctivitis, abdominal pain, septic shock, and multiorgan failure.
- The patient had a history of mild SARS-CoV-2 infection weeks prior to admission.
- Direct SARS-CoV-2 detection was negative, but IgG antibodies confirmed prior infection.
Findings:
- The patient received intensive care including immunoglobulin, aspirin, and steroid therapy.
- Clinical stabilization and complete recovery without sequelae were achieved.
- This case represents one of the earliest documented PIMS cases in Hungary.
Implications:
- PIMS is an important consideration in pediatric patients with severe sepsis and multiorgan failure post-SARS-CoV-2.
- Serological testing is crucial for diagnosing PIMS when viral detection is negative.
- Prompt, targeted therapy is essential for favorable outcomes in PIMS patients.
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