Key result
COVID-19 infection triggers fulminant dermatomyositis-like myocarditis with severe lymphocytic infiltration 32 days post-illness.
Why the study?
Myocarditis as a complication of post-acute COVID-19 syndrome is rarely reported and its association with dermatomyositis remains unclear.
Case Report (n=1)
This case report provides the first pathological evidence suggesting that fulminant myocarditis in post-acute COVID-19 syndrome may share features with dermatomyositis-like myocarditis.
May suggest dermatomyositis-like features in post-COVID myocarditis; hypothesis-generating and should not yet change practice.
Myocarditis is often reported as a complication of COVID-19 infection or post-vaccination, but there are few reports of "myocarditis for Post-acute COVID-19 syndrome", and many unknowns still remain. Apart from that, an association between COVID-19 infection and dermatomyositis has also been reported. We describe the clinical presentation of acute myocarditis in a patient who had developed COVID-19 syndrome one-month earlier. A healthy 49-year-old man experienced typical COVID-19 symptoms. Thirty-two days later, he was admitted because of fever and severe fatigue, chest pain and bradycardia. Blood tests showed major inflammation. PCR for SARS-CoV-2 on nasopharyngeal swab (ID NOW™) was positive, but diagnosed as a previous infection due to a high CT value. Because of haemodynamic worsening with both an increase in cardiac troponin I and NT-pro BNP levels and reduced wall motion on echocardiography, acute myocarditis was suspected. Myocardial biopsy revealed severe lymphocytic infiltration and interstitial edema between myocardial fibers. These findings led to the diagnosis of fulminant myocarditis. Interestingly, myocardium was also stained with human myxovirus resistance protein 1 (MxA). We consider that there may be an aspect of "dermatomyositis-like myocarditis with SARS-CoV-2" in our case. This is the first case of fulminant myocarditis for Post-acute COVID-19 syndrome in which diagnosis of active myocarditis was proven by pathological examination following myocardial biopsy and strong association with dermatomyositis was suggested pathologically.
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Kinoshita et al. (2023) conducted a case report in Post-acute COVID-19 syndrome / acute myocarditis (n=1). SARS-CoV-2 infection was evaluated on Development of fulminant myocarditis. A 49-year-old man developed fulminant, dermatomyositis-like myocarditis with severe lymphocytic infiltration and MxA staining 32 days after COVID-19 infection.
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