Key result
CMR identifies sequential LV aneurysms in a pathogenic DES variant carrier suggesting cytoskeletal genetic cardiomyopathy.
Case Report (n=1)
Recurrent nonischemic left ventricular aneurysms can be accurately identified by CMR and may be associated with pathogenic DES variants, suggesting a cytoskeletal genetic cardiomyopathy.
May support CMR-guided surgical repair in young patients with apical aneurysms; leaves open long-term outcomes and etiology.
BACKGROUND: Cardiac magnetic resonance (CMR) is the gold-standard technique for characterizing nonischemic structural cardiomyopathies, offering tissue characterization and precise localization of myocardial injury. CASE SUMMARY: A 24-year-old man presented with recurrent chest discomfort and tachyarrhythmias. Initial CMR revealed an apical left ventricular aneurysm with imaging features consistent with a true aneurysm and normal coronary arteries, successfully treated surgically. Five years later, recurrent ventricular tachycardia prompted re-evaluation; CMR identified a new inferolateral basal aneurysm in a region previously normal on postoperative imaging. Coronary computed tomography angiography again showed normal epicardial coronary arteries. Surgical patch repair and implantable cardioverter-defibrillator placement were performed. Genetic testing revealed a pathogenic desmin (DES) c.785A>T (p.Glu262Val) variant and additional variant of unknown significance in VCL and CDH2. DISCUSSION: The identification of a pathogenic DES variant suggests a potential underlying susceptibility to structural remodeling, although causality cannot be confirmed. TAKE-HOME MESSAGES: CMR was crucial in identifying sequential, anatomically distinct left ventricular aneurysms. The combination of recurrent nonischemic aneurysms and a pathogenic DES variant suggests a possible cytoskeletal genetic cardiomyopathy with arrhythmic risk.
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Garcia et al. (2026) conducted a case report in Recurrent Nonischemic Left Ventricular Aneurysms (n=1). Cardiac magnetic resonance and genetic testing was evaluated. Cardiac magnetic resonance identified sequential, anatomically distinct left ventricular aneurysms in a 24-year-old man with a pathogenic DES variant, suggesting a cytoskeletal genetic cardiomyopathy.
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