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Fulminant Myocarditis After mRNA COVID-19 Vaccine Evolving to Giant Cell Myocarditis
Erika Ouimet-Grennan1, Marie-Claude Parent1, Maxime Tremblay-Gravel1
1Department of Medicine, Division of Cardiology, Montreal Heart Institute, University of Montreal, Montreal, Quebec, Canada.
Background:
Pediatric inflammatory multisystem syndrome (PIMS-TS) is a rare entity observed in children with postinfectious hyperinflammatory syndrome. Cases have been reported, although rarely, after the mRNA SARS-CoV-2 (COVID-19) vaccine.
Case Summary:
We present a case of a young man who developed PIMS-TS with fulminant myocarditis after a first dose of COVID-19 vaccination, with persistent evidence of inflammation despite multiple lines of therapy over the course of 2 years. He then experienced fulminant myocarditis that was resistant to anti-inflammatory therapies. Repeat endomyocardial biopsy was consistent with giant cell myocarditis.
Discussion:
Cases of giant cell myocarditis after COVID-19 vaccination have been reported in the past, however to our knowledge, none have been reported 2 years after a single dose and with intercurrent diagnosis of PIMS-TS myocarditis. This raises the question of a possible pathophysiologic association between the 2 diseases and immune dysregulation.
Take-Home Message:
This case illustrates the importance of repeating the investigation and questioning the diagnosis when the progression of the disease is not typical.
Insights
Pediatric inflammatory multisystem syndrome (PIMS-TS) can rarely occur after COVID-19 vaccination. A case report details PIMS-TS with myocarditis developing two years after a single vaccine dose, suggesting potential immune dysregulation.
Area of Science:
- Cardiology
- Immunology
- Vaccinology
Background:
- Pediatric inflammatory multisystem syndrome (PIMS-TS) is a rare post-infectious hyperinflammatory syndrome in children.
- While rare, PIMS-TS cases have been documented following mRNA SARS-CoV-2 (COVID-19) vaccination.
Observation:
- A young male developed PIMS-TS with fulminant myocarditis after his first COVID-19 vaccine dose.
- The condition persisted for two years, showing resistance to multiple anti-inflammatory treatments.
- A repeat endomyocardial biopsy confirmed giant cell myocarditis.
Findings:
- This case presents PIMS-TS with myocarditis occurring two years post-vaccination, a timeline not previously reported.
- Giant cell myocarditis was diagnosed, a condition known to be associated with COVID-19 vaccination but typically with shorter latency.
Implications:
- The prolonged interval and specific diagnosis raise questions about a potential pathophysiological link between COVID-19 vaccination, PIMS-TS, and immune dysregulation.
- This case underscores the importance of re-evaluation and diagnostic questioning in atypical disease progressions.
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