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Apical hypertrophic cardiomyopathy: diagnosis with contrast-enhanced echocardiography--a case report

Esmeray Acartürk1, Abdi Bozkurt, Yurdaer Dönmez

  • 1Cukurova University, School of Medicine, Department of Cardiology, Adana, Turkey. kanarya@mail.cu.edu.tr

Angiology
|June 6, 2003
PubMed

Insights

Apical hypertrophic cardiomyopathy (HCM) is a rare heart condition. Contrast-enhanced echocardiography aids in diagnosing this condition, which can mimic ischemic heart disease.

Area of Science:

  • Cardiology
  • Medical Imaging

Background:

  • Apical hypertrophic cardiomyopathy (HCM) is a distinct variant of hypertrophic cardiomyopathy.
  • It is characterized by a unique spade-like configuration on left ventriculography.
  • Diagnosis can be challenging, potentially mimicking apical akinesia or thrombus, especially with poor acoustic windows.

Observation:

  • A 50-year-old woman presented with symptoms suggestive of ischemic heart disease, including typical angina and specific electrocardiogram (ECG) findings (T wave inversion in V3-V6, II, III, aVF) alongside left ventricular hypertrophy.
  • Initial diagnostic evaluations were complicated by the patient's acoustic window limitations.

Findings:

  • Contrast-enhanced echocardiography proved effective in diagnosing apical HCM.
  • The diagnosis was definitively confirmed by identifying the characteristic spade-like morphology on left ventriculography.

Implications:

  • Apical HCM should be considered in the differential diagnosis for patients presenting with symptoms and ECG patterns resembling ischemic heart disease.
  • Contrast-enhanced echocardiography is highlighted as a reliable and straightforward diagnostic method for apical HCM.

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