Key result
Serial CMR over 20 years tracks the long-term progression of lateral wall HCM.
Why the study?
There is little knowledge of the long-term evolution of hypertrophic cardiomyopathy as visualized by magnetic resonance imaging.
Case Report (n=1)
This case report demonstrates the long-term evolution of a rare variant of hypertrophic cardiomyopathy over 20 years using cardiac MRI.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for rare lateral-wall HCM; larger prospective cohorts needed before any clinical adoption.
We are reporting a long-time magnetic resonance imaging (MRI) follow-up in a rare case of cardiac left lateral wall hypertrophy. Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disorder and a significant cause of sudden cardiac death. Cardiac magnetic resonance (CMR) imaging can be a valuable tool for assessment of detailed information on size, localization, and tissue characteristics of hypertrophied myocardium. However, there is still little knowledge of long-term evolution of HCM as visualized by magnetic resonance imaging. Recently, our group reported a case of left lateral wall HCM as a rare variant of the more common forms, such as septal HCM, or apical HCM. As we now retrieved an old cardiac MRI acquired in this patient more than 20 years ago, we are able to provide the thrilling experience of an ultra-long MRI follow-up presentation in this rare case of left lateral wall hypertrophy. Furthermore, this case outlines the tremendous improvements in imaging quality within the last two decades of CMR imaging.
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Tobias Gassenmaier (2015) conducted a case report in Atypical left lateral wall hypertrophic cardiomyopathy (n=1). Cardiac magnetic resonance (CMR) imaging was evaluated on Long-term evolution of MRI characteristics. Cardiac magnetic resonance imaging follow-up over 20 years in a single patient demonstrated the long-term evolution of a rare case of left lateral wall hypertrophic cardiomyopathy.
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