[Repeated changes of electrocardiogram caused by Takotsubo-type cardiomyopathy: a case with hypertrophic

Seigo Miyoshi1, Yuji Hara, Akiyoshi Ogimoto

  • 1Second Department of Internal Medicine, Ehime University School of Medicine.

Insights

This study discusses a patient with hypertrophic nonobstructive cardiomyopathy who experienced recurrent electrocardiogram (ECG) abnormalities. These changes, including T-wave inversions and QT interval prolongation, were ultimately attributed to Takotsubo-type cardiomyopathy.

Area of Science:

  • Cardiology
  • Cardiovascular Imaging
  • Electrophysiology

Background:

  • A 67-year-old woman with a history of hypertrophic nonobstructive cardiomyopathy presented with recurrent electrocardiogram (ECG) abnormalities.
  • Initial ECG showed T-wave abnormalities, improving at consultation, with echocardiography revealing apical hypertrophy.

Observation:

  • The patient experienced chest discomfort with significant ECG changes: negative T-waves in multiple leads and QT interval prolongation.
  • Left ventriculography confirmed apical hypertrophy without wall motion abnormalities; coronary angiography ruled out significant stenosis.
  • I-123 MIBG scintigraphy indicated marked perfusion defects at the left ventricular apex.

Findings:

  • ECG findings demonstrated dynamic changes, including T-wave inversion and QT interval prolongation, suggestive of cardiac stress.
  • Diagnostic imaging revealed left ventricular apical hypertrophy and myocardial perfusion defects, but no obstructive coronary artery disease.
  • Resolution of ECG abnormalities, including QT interval shortening and decreased T-wave negativity, was observed over five months.

Implications:

  • The case highlights the potential for Takotsubo-type cardiomyopathy to mimic or coexist with hypertrophic cardiomyopathy.
  • Recognizing dynamic ECG changes and perfusion defects is crucial for diagnosing Takotsubo cardiomyopathy in patients with underlying cardiac conditions.
  • This presentation underscores the importance of comprehensive diagnostic evaluation for complex cardiac presentations.

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
Disturbances in Heart Rhythm01:29

Disturbances in Heart Rhythm

Arrhythmia or dysrhythmia refers to an abnormal heart rhythm caused by a defect in the heart's conduction system. It can cause the heart to beat irregularly, too quickly, or too slowly, leading to symptoms like chest pain, shortness of breath, and fainting. Factors such as stress, caffeine, alcohol, nicotine, cocaine, certain drugs, congenital defects, diseases, and electrolyte abnormalities can trigger arrhythmias.
Arrhythmias are categorized by their speed, rhythm, and origin. A slow heart...
Dysrhythmias III: Characteristics of Dysrhythmias01:29

Dysrhythmias III: Characteristics of Dysrhythmias

Dysrhythmias, also known as arrhythmias, are irregular heart rhythms that result from abnormal electrical activity in the heart, affecting its ability to circulate blood efficiently. Tachyarrhythmias, a subset of dysrhythmias, are characterized by abnormally fast heart rates exceeding 100 beats per minute. Here are some types of tachyarrhythmias with their distinct ECG features:Sinus Tachycardia:Sinus tachycardia presents a regular heart rhythm with an increased rate of 101-180 beats per minute.