Key result
TTE and CMR successfully diagnose LVNC in a 28-year-old male with heart failure.
Why the study?
Left ventricular noncompaction cardiomyopathy is a rare congenital disorder with distinctive myocardial features and clinical complications that require detailed diagnostic evaluation.
Case Report (n=1)
This case report highlights the utility of multimodality imaging (TTE and CMR) in diagnosing left ventricular noncompaction cardiomyopathy in a young adult presenting with new-onset heart failure.
Novel LVNC imaging features may refine diagnosis; leaves open prospective validation for risk stratification.
Left ventricular noncompaction cardiomyopathy (LVNC) or spongy myocardium is a rare congenital disorder prominently distinguished by deep abnormal trabeculations and intertrabecular recesses which communicate with the ventricular cavity that can be detected on Transthoracic Echocardiography (TTE) or cardiac MRI (CMR) studies. LVNC can occur in isolation or coexists with other cardiac and/or systemic anomalies and the common clinical complications are heart failure, arrhythmias, and cardio embolism. The American Heart Association classified it as a primary genetic cardiomyopathy. We described the case of a 28years old young adult who presented with heart failure for the first time. Transthoracic echocardiography showed a trabeculated, sponge-like appearance of the ventricular apical and inferolateral segments. Following evaluation with CMR imaging revealed non compaction of the left ventricle. Here we discussed the diagnosis of this case and reviewed the medical literature that concerned to LVNC.
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Ravi Sahi (2021) conducted a case report in Left ventricular noncompaction cardiomyopathy (LVNC) (n=1). Guideline-directed medical therapy and AICD advice was evaluated. A 28-year-old male with heart failure was successfully diagnosed with left ventricular noncompaction cardiomyopathy using echocardiography and cardiac MRI, and managed with medical therapy.
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