| Condition[1]
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Features
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Example
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| Arrythmogene right ventricular cardiomyopathy (ARVC)
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- Fibrofatty degeneration of the RV.
- Myocardial degeneration leads to RV dilation and poor RVF.
- Ventricular fibrillation by slow conduction velocities, guide block and spatial variation in conduction velocity.
- Aneurysms of the RV free wall.
- Echodense moderator band and myocardial RV free wall.
- Genetic component
- Rare 1:5000 people.
|
Video
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| Echodense RV free wall for suspected ARVC
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|
| Decreased RV strain in ARVC
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| Dilated cardiomyopathy (DCM)
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- It is the most common form of cardiomyopathy.
- Also known as congestive cardiomyopathy.
- Poor LVF and LV dilatation.
- Arrhythmias (atrial fibrillation 20-30%).
- Clot formation, which may lead to thrombo-embolic complications.
- Often accompanied by pulmonary hypertension, dilation of other compartments, and an insufficiency of mitral and/or tricuspid valve
- Familial DCM's common to autosomal dominant, autosomal recessive and sex-linked inheritance.
- Causes:
- (post-) infectious: various viruses and bacteria, as at the final stage of myocarditis.
- intoxication: cocaine, alcohol abuse.
- iatrogenic: some chemostatica, X-ray radiation.
- Metabolic: vitamin B1 deficiency.
- -idiopathic: In approximately 30% of cases, no cause is found
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| Dilated LV on AP4CH
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| Dilated LV on PLAX
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|
| EPSS is a useful measurement to follow up DCM
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| Hypertrophic cardiomyopathy (HCM)
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- 65% asymmetric hypertrophy of the myocardium, usually ventricular septum sometimes apical involvement.
- 35% symmetrical hypertrophy of the myocardium (not to be confused with aortic stenosis or hypertension).
- Small LV lumen.
- Preserved systolic LV function (EF normal or slightly decreased)
- Diastolic dysfunction.
- Autosomal dominant progressive deviation from nature.
- Could be associated with sudden cardiac death due to ventricular fibrillation, an increased risk of thromboembolism.
- Heart failure can be caused by the rigidity of the thickened heart muscle (diastolic heart failure), by an obstruction in the LVOT (SAM) and is associated with mitral valvular insufficiency. The course of the disease is progressive.
- Occurs in persons 1:500-1000
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| Asymmetric hypertrophy
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| Symmetrical hypertrophy
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| Apical hypertrophy
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| Non-compaction cardiomyopathy (NCCMP)
|
- LV wall has a spongy appearance.
- Jenni criteria (Heart 2007).
- Also called insulated non compaction of the ventricular myocardium (INVM), it is a rare form of congenital heart disease in which the tissue of the ventricular myocardium is not well constructed in terms of texture.
- After HCM DCM, it is the most common cause of primary cardiomyopathy in children.
- It is a congenital defect, which occurs in the 20th week of pregnancy.
- The condition is expressed by heart failure, arrhythmias, and an increased risk of thrombus formation.
- The disorder often manifests itself later in life and has a high mortality rate due to heart failure and arrhythmias.
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| NCCMP with crypts and apical midventriculair
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| Video
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| NCCCMP on PSax
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| Restrictive cardiomyopathy
|
- Stiffened myocardium.
- This form comes after at least 1 and is usually associated with storage diseases, such as sarcoidosis, amyloidosis, and the like.
- Preserved systolic LVF. LV is not dilated.
- Diastolic dysfunction (see fig.)
- LV and RV may be hypertrophied.
- Dilated atria and VCI.
- Pulmonary hypertension.
- Myocardial echo during and amyloidosis speckled
|
|
| Abnormally low É in restrictive cardiomyopathy
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| Tako-tsubo cardiomyopathy
|
- Takotsubo is named after the ceramic pots used to trap octopus in Japan.
- Apical ballooning, akinetic of the apex. This gives the LV the octupus trap shape.
- Manifests itself as an acute myocardial infarction with ST elevations, however, no significant coronary artery disease.
- Is more common in women than in men, the average age of 62 to 75 years.
- Stress induced, is triggered by an acute illness or intense emotional or physical stress
- Also called "broken heart syndrome" or "Stress CMP".
- LV normalizes in a few days to several weeks.
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| Apical ballooning
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