Key result
MIS-A presents as a rare cause of STEMI with normal coronary arteries.
Why the study?
Multisystem inflammatory syndrome in adults (MIS-A) is an uncommon and under-recognized complication of SARS-CoV-2 infection with challenging management due to its unusual symptoms.
Case Report (n=1)
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Highlights MIS-A as a rare but important differential diagnosis for ST-segment elevation myocardial infarction with normal coronary arteries in patients with recent SARS-CoV-2 infection.
The COVID-19 pandemic is a significant worldwide health emergency. Due to the high incidence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, there are increasingly recognisable early and long-term outcomes of the disease. One of the uncommon complications of SARS-CoV-2 infection is multisystem inflammatory syndrome in adults (MIS-A). This is a post-sequela of SARS-CoV-2 infection associated with hyperinflammatory syndrome accompanied by extrapulmonary organ dysfunction. The prevalence of MIS-A ranges from 0.2% to 11.7% of the studied SARS-CoV-2 infection cases. The lack of awareness of this condition and unusual constellation of symptoms makes its management challenging. A 36-year-old woman who had a recent SARS-CoV-2 infection presented with chest pain and hypotension. An ECG showed ST-segment elevation in the anteroseptal wall, elevated cardiac enzymes and inflammatory markers. Transthoracic echocardiogram revealed segmental hypokinesia with a mildly reduced ejection fraction of 41%. Coronary angiogram showed normal arteries. A diagnosis of MIS-A was considered and the patient was started on steroids and IV immunoglobulin.
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David et al. (2023) conducted a case report in Multisystem Inflammatory Syndrome in Adults (MIS-A) with ST-Segment Elevation MI (n=1). Steroids and IV immunoglobulin was evaluated. Multisystem inflammatory syndrome in adults (MIS-A) presented as a rare cause of ST-segment elevation myocardial infarction with normal coronary arteries in a 36-year-old woman.
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