Related Experiment Video
Updated: Jul 27, 2025

Morphological and Functional Assessment of the Right Ventricle Using 3D Echocardiography
Published on: October 28, 2020
Diagnosis and Clinical Implication of Left Ventricular Aneurysm in Hypertrophic Cardiomyopathy
Errico Federico Perillo1, Grazia Canciello1, Felice Borrelli1
1Department of Advanced Biomedical Sciences, Federico II University, 80131 Naples, Italy.
Insights
Hypertrophic cardiomyopathy (HCM) can cause left ventricular (LV) apical aneurysms, a poor prognostic marker. This review explores the mechanisms, diagnosis, and clinical implications of LV aneurysms in HCM patients.
Area of Science:
- Cardiology
- Genetics
- Pathophysiology
Background:
- Hypertrophic cardiomyopathy (HCM) is a genetic heart condition with varied presentations.
- A subset of HCM patients develop left ventricular (LV) apical aneurysms (2-5% prevalence).
- LV apical aneurysms involve apical dyskinesis/akinesis and scarring, distinct from coronary artery disease.
Purpose of the Study:
- To review the pathomechanism of LV apical aneurysms in HCM.
- To discuss diagnostic approaches for LV apical aneurysms.
- To elucidate the clinical implications and prognostic significance of LV aneurysms in HCM.
Main Methods:
- Literature review of existing studies on HCM and LV apical aneurysms.
- Analysis of proposed pathomechanisms, including pressure-induced ischemia.
- Synthesis of diagnostic criteria and clinical outcomes.
Main Results:
- The leading hypothesis for LV aneurysm formation involves high systolic intra-aneurysmal pressure and impaired diastolic perfusion.
- LV apical aneurysm is recognized as a marker of poor prognosis in HCM.
- The effectiveness of treatments like anticoagulation or ICDs for this specific complication remains unclear.
Conclusions:
- LV apical aneurysms represent a significant complication of HCM with serious prognostic implications.
- Further research is needed to clarify the optimal management strategies for patients with HCM and LV apical aneurysms.
- Understanding the mechanism and diagnosis is crucial for patient care.
Abstract:
Hypertrophic cardiomyopathy (HCM) is a genetic disease with heterogeneous clinical presentation and prognosis. Within the broad phenotypic expression of HCM, there is a subgroup of patients with a left ventricular (LV) apical aneurysm, which has an estimated prevalence between 2% and 5%. LV apical aneurysm is characterized by an area of apical dyskinesis or akinesis, often associated with regional scarring. To date, the most accepted pathomechanism of this complication is, in absence of coronary artery disease, the high systolic intra-aneurysmal pressure, which, combined with impaired diastolic perfusion from lower stroke volume, results in supply-demand ischemia and myocardial injury. Apical aneurysm is increasingly recognized as a poor prognostic marker; however, the efficacy of prophylactic anticoagulation and/or intracardiac cardioverted defibrillator (ICD) in improving morbidity and mortality is not yet clearly demonstrated. This review aims to elucidate the mechanism, diagnosis and clinical implication of LV aneurysm in patients with HCM.
More Related Videos
Related Concept Videos
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Aortic Regurgitation II: Clinical Features and Diagnostic Tests
Mitral Stenosis II: Clinical features and Diagnostic Tests
Aneurysm II: Clinical Manifestations and Diagnostic Studies
Cardiomyopathy II: Dilated Cardiomyopathy
Mitral Regurgitation I: Introduction

