ArticleEuropean heart journal. Case reports2025
Saw-tooth cardiomyopathy from foetal to neonatal period: a case report and literature review.
Article in European heart journal. Case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Saw-tooth cardiomyopathy is a rare condition characterized by left ventricular (LV) dysplasia, defined by multiple myocardial crypts resembling a 'saw-tooth' pattern on imaging examinations. Case Summary: We present a case involving a 10-day-old neonate who was diagnosed with saw-tooth cardiomyopathy, a diagnosis substantiated by echocardiography, computed tomography (CT), and cardiac magnetic resonance imaging (CMR). The patient demonstrated arrhythmia characterized by premature atrial contractions and had a suspected cardiomyopathy identified during the foetal period. Discussion: The diagnosis of this condition is solely based on morphological features and may be misdiagnosed as LV non-compaction. Imaging modalities, including echocardiography, CT, and CMR are valuable diagnostic tools. Owing to its rarity and unclear pathogenesis, the prognosis of saw-tooth cardiomyopathy remains uncertain, necessitating long-term, potentially lifelong follow-up.
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