Apical variant hypertrophic cardiomyopathy "multimodality imaging evaluation"

Gary Huang1, Shaimaa A Fadl2, Stan Sukhotski3,4

  • 1Department of Cardiology, University of Washington Medical Center, Seattle, WA, USA.

Insights

Apical variant hypertrophic cardiomyopathy (AHCM) is diagnosed using echocardiography, cardiac MRI, and CT. Recognizing specific imaging patterns aids in accurate diagnosis and avoids unnecessary tests.

Area of Science:

  • Cardiology
  • Medical Imaging

Background:

  • Apical variant hypertrophic cardiomyopathy (AHCM) involves asymmetric left ventricular (LV) apex hypertrophy.
  • EKG findings include T wave inversions and LV hypertrophy (LVH).

Purpose of the Study:

  • To review imaging features of AHCM across various modalities.
  • To assess the diagnostic value of each imaging modality for AHCM.

Main Methods:

  • Echocardiography with contrast for LV apex visualization.
  • Cardiac magnetic resonance (CMR) for tissue characterization and LGE sequences.
  • Cardiac computed tomography (CCT) for coronary arteries and cardiac anatomy.
  • Myocardial perfusion imaging (MPI) for characteristic patterns like "Solar Polar" map.

Main Results:

  • Echocardiography defines AHCM by LV apex wall thickness (≥ 15 mm) or apical-to-basal ratio (≥ 1.3).
  • CMR identifies myocardial scarring via LGE.
  • CCT assesses coronary arteries and cardiac structure.
  • MPI reveals specific patterns in AHCM, aiding diagnosis.

Conclusions:

  • Accurate recognition of AHCM imaging patterns is crucial for diagnosis.
  • Utilizing appropriate imaging modalities can prevent unnecessary investigations.

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