Noncompaction cardiomyopathy (Q42742): Difference between revisions
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A cardiomiopatia não compactada é uma anormalidade morfológica do miocárdio que afeta predominantemente o ápice do ventrículo, caracterizada por hipertrabeculação e recessos intertrabeculares profundos, geralmente acompanhados por uma camada subepicárdica anormalmente fina de miocárdio compactado, que geralmente, mas nem sempre, está associada à disfunção ventricular. _x000D_ _x000D_ Informações adicionais. A cardiomiopatia não compactada envolve classicamente o ventrículo esquerdo, mas também pode envolver apenas o ventrículo direito ou ambos. Pode ocorrer como um achado isolado ou em associação com um fenótipo cardiomiopático dilatado, hipertrófico ou misto. Foi descrita em associação a cardiopatia congênita complexa, anomalias das artérias coronárias e como um achado isolado, com e sem anormalidades musculoesqueléticas e outras anormalidades sistêmicas. | |||
| description / en | description / en | ||
Noncompaction cardiomyopathy is a morphologic abnormality of the myocardium predominantly affecting the apex of the ventricle characterised by hypertrabeculation and deep inter-trabecular recesses, usually accompanied by an abnormally thin subepicardial layer of compacted myocardium, that is generally but not always associated with ventricular dysfunction. Additional information. Noncompaction cardiomyopathy classically involves the left ventricle but can also involve only the right ventricle or both. It can occur as an isolated finding or in association with a dilated, hypertrophic, or mixed cardiomyopathic phenotype. It has been described in association with complex congenital heart disease, coronary artery anomalies and as an isolated finding, with and without musculoskeletal and other system abnormalities. | |||
Revision as of 09:23, 13 August 2026
Noncompaction cardiomyopathy is a morphologic abnormality of the myocardium predominantly affecting the apex of the ventricle characterised by hypertrabeculation and deep inter-trabecular recesses, usually accompanied by an abnormally thin subepicardial layer of compacted myocardium, that is generally but not always associated with ventricular dysfunction. Additional information. Noncompaction cardiomyopathy classically involves the left ventricle but can also involve only the right ventricle or both. It can occur as an isolated finding or in association with a dilated, hypertrophic, or mixed cardiomyopathic phenotype. It has been described in association with complex congenital heart disease, coronary artery anomalies and as an isolated finding, with and without musculoskeletal and other system abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | BC44 |
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| English | Noncompaction cardiomyopathy |
Noncompaction cardiomyopathy is a morphologic abnormality of the myocardium predominantly affecting the apex of the ventricle characterised by hypertrabeculation and deep inter-trabecular recesses, usually accompanied by an abnormally thin subepicardial layer of compacted myocardium, that is generally but not always associated with ventricular dysfunction. Additional information. Noncompaction cardiomyopathy classically involves the left ventricle but can also involve only the right ventricle or both. It can occur as an isolated finding or in association with a dilated, hypertrophic, or mixed cardiomyopathic phenotype. It has been described in association with complex congenital heart disease, coronary artery anomalies and as an isolated finding, with and without musculoskeletal and other system abnormalities. |
