Dilated cardiomyopathy due to congenital anomaly of coronary artery (Q42276): Difference between revisions
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Cardiomiopatia dilatada devida a uma anomalia congênita de uma ou mais artérias coronárias, como origem anômala da artéria coronária esquerda anômala saindo da artéria pulmonar (ALCAPA), estenose ou atresia do óstio coronário, circulação coronária dependente do ventrículo direito na atresia pulmonar com septo ventricular íntegro. É uma forma de cardiomiopatia isquêmica que causa disfunção ventricular sistólica que se relaciona a um espectro de equilíbrio e desequilíbrio entre perfusão e contração, incluindo infarto do miocárdio, miocárdio atordoado, miocárdio hibernante e cicatrizes. | |||
| description / en | description / en | ||
Dilated cardiomyopathy due to a congenital anomaly of one or more coronary arteries, such as anomalous left coronary artery from pulmonary artery (ALCAPA), coronary ostial stenosis or atresia, right ventricular dependent coronary circulation in pulmonary atresia with an intact ventricular septum. It is a form of ischaemic cardiomyopathy causing systolic ventricular dysfunction that relates to a spectrum of perfusion contraction matching and mismatching, including myocardial infarction, stunning, hibernation and scarring. | |||
Revision as of 08:43, 13 August 2026
Dilated cardiomyopathy due to a congenital anomaly of one or more coronary arteries, such as anomalous left coronary artery from pulmonary artery (ALCAPA), coronary ostial stenosis or atresia, right ventricular dependent coronary circulation in pulmonary atresia with an intact ventricular septum. It is a form of ischaemic cardiomyopathy causing systolic ventricular dysfunction that relates to a spectrum of perfusion contraction matching and mismatching, including myocardial infarction, stunning, hibernation and scarring.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | BA51.0 |
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| English | Dilated cardiomyopathy due to congenital anomaly of coronary artery |
Dilated cardiomyopathy due to a congenital anomaly of one or more coronary arteries, such as anomalous left coronary artery from pulmonary artery (ALCAPA), coronary ostial stenosis or atresia, right ventricular dependent coronary circulation in pulmonary atresia with an intact ventricular septum. It is a form of ischaemic cardiomyopathy causing systolic ventricular dysfunction that relates to a spectrum of perfusion contraction matching and mismatching, including myocardial infarction, stunning, hibernation and scarring. |
