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Mid-ventricular hypertrophic cardiomyopathy with apical aneurysm: a multimodality imaging case report
Pavel Martinez-Dominguez1,2, Manuel Horna-Noriega3, María José Santa-Ana-Bayona1
1Departamento de Cardiología Nuclear, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México. Departamento de Cardiología Nuclear Instituto Nacional de Cardiología Ignacio Chávez Ciudad de México México.
Insights
Mid-ventricular hypertrophic cardiomyopathy, a rare condition, can cause apical aneurysms and increase risks for cardiac arrest and sudden cardiac death. This case highlights diagnosis and management strategies for this challenging cardiomyopathy.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Genetics
Background:
- Hypertrophic cardiomyopathy (HCM) is a primary myocardial disease.
- Mid-ventricular HCM is a rare variant characterized by hypertrophy predominantly in the mid-ventricle.
- Apical aneurysms can be a presenting feature of mid-ventricular HCM.
Observation:
- A 41-year-old male presented with exertional dyspnea and syncope.
- Multimodality imaging, including echocardiography and cardiac magnetic resonance, revealed mid-ventricular hypertrophy.
- An apical aneurysm was identified in conjunction with the ventricular hypertrophy.
Findings:
- The imaging findings confirmed the diagnosis of mid-ventricular hypertrophic cardiomyopathy with apical aneurysm.
- This specific subtype of HCM is associated with a heightened risk of adverse cardiac events.
- Potential complications include heart failure, thromboembolic events, cardiac arrest, and sudden cardiac death.
Implications:
- Early recognition and diagnosis of mid-ventricular HCM with apical aneurysm are crucial.
- Risk stratification and appropriate management, such as ICD implantation, are vital for preventing sudden cardiac death.
- Further research into the pathophysiology and long-term outcomes of this rare condition is warranted.
Abstract:
Mid-ventricular hypertrophic cardiomyopathy is a rare subgroup within hypertrophic cardiomyopathies that may present with apical aneurysm. This condition is associated with an increased risk of cardiac adverse events, including cardiac arrest, heart failure, thromboembolic events, or sudden cardiac death. We present a case of a 41-year-old man who presented with a history of exertional dyspnea and syncope. Multimodality imaging with echocardiography and cardiac magnetic resonance showed hypertrophy of the mid-ventricular segments with apical aneurysm. An implantable cardioverter-defibrillator was implanted to prevent sudden cardiac death.
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