An unusual case of isolated non-compacted right ventricular myocardium
Isolated ventricular non-compaction is a rare type of cardiomyopathy resulting from arrested myocardial development during embryogenesis. This rare entity can be easily diagnosed by characteristic appearance of prominent myocardial trabeculations and deep inter-trabecular spaces. The clinical manife...
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Veröffentlicht in: | European journal of echocardiography 2008-05, Vol.9 (3), p.424-425 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Isolated ventricular non-compaction is a rare type of cardiomyopathy resulting from arrested myocardial development during embryogenesis. This rare entity can be easily diagnosed by characteristic appearance of prominent myocardial trabeculations and deep inter-trabecular spaces. The clinical manifestations include heart failure signs, ventricular arrhythmias, and cardio-embolic events. Although the usual site of involvement is the left ventricle, the right ventricle (RV) can rarely be affected. Here, we report a case of 23-year-old male patient with isolated RV non-compaction. |
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ISSN: | 1525-2167 1532-2114 |
DOI: | 10.1093/ejechocard/jen016 |