Cardiac MRI in a patient with coincident left ventricular non-compaction and hypertrophic cardiomyopathy
Journal of Tehran University Heart Center [The]. 2011; 6 (4): 214-216
en Inglés
| IMEMR
| ID: emr-146545
ABSTRACT
Left ventricular non-compaction cardiomyopathy is a rare congenital cardiomyopathy that affects both children and adults. Since the clinical manifestations are not sufficient to establish diagnosis, echocardiography is the diagnostic tool that makes it possible to document ventricular non-compaction and establish prognostic factors. We report a 47-year-old woman with a history of dilated cardiomyopathy with unknown etiology. Echocardiography showed mild left ventricular enlargement with severe systolic dysfunction [EF = 20-25%]. According to cardiac magnetic resonance imaging findings non-compaction left ventricle with hypertrophic cardiomyopathy was considered, and right ventricular septal biopsy was recommended. Right ventricular endomyocardial biopsy showed moderate hypertrophy of cardiac myocytes with foci of myocytolysis and moderate interstitial fibrosis. No evidence of infiltrative deposition was seen
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Imagen por Resonancia Magnética
/
Puente Cardiopulmonar
/
Arteria Carótida Común
/
Paro Circulatorio Inducido por Hipotermia Profunda
/
Cardiomiopatías
Tipo de estudio:
Informe de Casos
Límite:
Humanos
/
Masculino
Idioma:
Inglés
Revista:
J. Tehran Univ. Heart Cent.
Año:
2011
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