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[Atypical hypertrophic cardiomyopathy with calcified, left ventricular apical thrombosis]

R Gradaus1, M Lentschig, T Wichter

  • 1Med. Klinik und Poliklinik, Westfälische Wilhelms-Universität Münster.

Zeitschrift Fur Kardiologie
|July 17, 1999
PubMed

Insights

This case report details an asymptomatic patient with atypical hypertrophic cardiomyopathy (HCM). An abnormal ECG led to the discovery of a calcified apical thrombus within the left ventricle.

Area of Science:

  • Cardiology
  • Medical Imaging

Background:

  • Hypertrophic cardiomyopathy (HCM) is a genetic heart muscle disease.
  • Atypical presentations of HCM can pose diagnostic challenges.

Observation:

  • An asymptomatic 42-year-old patient presented with an abnormal electrocardiogram (ECG) showing giant negative T-waves and high QRS voltages.
  • Chest imaging revealed apical calcification.
  • Echocardiography and left ventricular (LV) cineangiography demonstrated apical LV hypertrophy and cavity obliteration.

Findings:

  • Magnetic resonance imaging (MRI) confirmed a calcified thrombus within the apical LV cavity.
  • The findings were consistent with an atypical form of hypertrophic cardiomyopathy.

Implications:

  • This case highlights the importance of advanced imaging in diagnosing rare HCM variants.
  • Recognition of apical thrombus in HCM is crucial for risk stratification and management.
  • Further research into the specific mechanisms of thrombus formation in atypical HCM is warranted.

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