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Journal of Rare Cardiovascular Diseases
ISSN: 2299-3711 (Print)
e-ISSN: 2300-5505 (Online)
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Accidentally discovered non‑compaction cardiomyopathy in patient with initial diagnosis of acute coronary syndrome (RCD code: III-5A)
Aleksander Trąbka‑Zawicki
,  
Andrzej Gackowski
,  
Marek Andres
,  
Aleksander Zeliaś
,  
Magdalena Kostkiewicz
,  
Igor Tomala
,  
Jacek Lelakowski
,  
Krzysztof Żmudka
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Abstract
Isolated non‑compaction cardiomyopathy is a rare congenital developmental disorder, which belongs to the group of unclassified cardiomyopathies by the ESC Position Statement. Typical echocardiographic findings include multiple trabeculations of the left ventricular muscle, separated by deep lacunae which communicate with left ventricular lumen. We present a case of accidentally discovered non‑compaction cardiomyopathy in a 46‑year‑old male, who was initially diagnosed with an acute coronary syndrome. The diagnosis of the left ventricular non‑compaction was confirmed by transthoracic echocardiography and cardiac magnetic resonance. Occupational contribution (lead and zinc exposure and repeated electric shocks) to the onset of the heart failure was additionally evaluated. JRCD 2013; 1 (3): 17–22
Keywords
cardiomyopathy non‑compaction; congenital heart defects; heart failure
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Keywords
Classification of Rare Cardiovascular Diseases anticoagulation atrial fibrillation atrial septal defect cardiomyopathy computed tomography congenital heart disease echocardiography electrocardiogram electrocardiography heart failure implantable cardioverter‑defibrillator magnetic resonance imaging pregnancy pulmonary arterial hypertension pulmonary hypertension rare cardiovascular disease rare disease right heart catheterization right ventricular failure
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