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Disseminated Blastomycosis Presenting with Spontaneous Coronary Artery Dissection
Rahul Sehgal1, D Fearghas O'Cochlain2, Andrew R Virata3
1Department of Rheumatology, Mayo Clinic Alix School of Medicine, Mayo Clinic Health System, Eau Claire, Wisconsin, USA.
Insights
Severe infection-induced systemic inflammation may cause spontaneous coronary artery dissection (SCAD), a condition often seen in acute coronary syndrome. This case highlights blastomycosis as a potential trigger for SCAD.
Area of Science:
- Cardiology
- Infectious Diseases
- Immunology
Background:
- Spontaneous coronary artery dissection (SCAD) is an emerging cause of acute coronary syndrome (ACS) and myocardial infarction (MI).
- The link between infection-induced systemic inflammation and SCAD is not well-established, unlike autoimmune disorders.
- SCAD typically affects individuals without traditional atherosclerotic risk factors.
Purpose of the Study:
- To present a case of SCAD precipitated by systemic inflammation from disseminated blastomycosis.
- To explore the potential role of severe infections as a trigger for SCAD.
Main Methods:
- Case report of a 49-year-old woman with ST-elevation myocardial infarction (STEMI).
- Diagnosis of SCAD was made based on clinical presentation and imaging.
- Confirmation of disseminated blastomycosis via skin biopsy and synovial fluid culture for *Blastomyces dermatitidis*.
Main Results:
- The patient presented with STEMI attributed to SCAD.
- The SCAD was associated with a severe systemic inflammatory response due to disseminated blastomycosis.
- Identification of *Blastomyces dermatitidis* confirmed the infectious etiology.
Conclusions:
- Systemic inflammation from severe infections, such as blastomycosis, should be considered a potential cause of SCAD.
- Cardiac involvement is a rare but serious complication of blastomycosis.
- Coronary revascularization may be necessary for SCAD patients experiencing hemodynamic instability or worsening ischemia.
Abstract:
Spontaneous coronary artery dissection (SCAD) is increasingly recognized as an important cause of acute coronary syndrome (ACS) and myocardial infarction (MI) in individuals with few or no known atherosclerotic risk factors. While systemic autoimmune inflammatory disorders are associated with precipitating SCAD, the role of infection-induced systemic inflammation in SCAD is not well defined. We present the case of a 49-year-old Caucasian woman with ST-elevation myocardial infarction (STEMI) diagnosed as SCAD from a severe systemic inflammatory response related to disseminated blastomycosis. Punch biopsy of a skin lesion and synovial fluid culture confirmed Blastomyces dermatitidis. This case suggests the possibility of systemic infection-induced inflammation as a precipitating factor in SCAD pathogenesis similar to autoimmune inflammatory disorders.
Learning Points:
Recognize the role of systemic inflammation from severe infection as a possible cause of spontaneous coronary artery dissection (SCAD).Recognize that cardiac involvement is rare in blastomycosis.Coronary revascularization may be required in SCAD for haemodynamic instability, ischaemic chest pain progression, and myocardium at risk.
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