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Authors:
Jerzy Wojciuk, Ravish Katira, Ranjit S More, Roger W Bury
The authors describe a case of Takotsubo-like syndrome in a 59-year-old Caucasian woman.
A 59-year-old woman was admitted with symptoms and signs suggesting acute coronary syndrome. A 12-lead electrocardiogram (ECG) demonstrated ST segment elevation in leads V2-V6, I, II and aVL consistent with ST segment elevation myocardial infarction. She underwent emergency coronary angiography, which demonstrated only minor irregularities in coronaries. Chest pain resolved completely after four hours.

Figure 1b. Transthoracic echocardiography during the initial admission (apical four-chamber view, diastole)

Figure 1a. Transthoracic echocardiography during the initial admission (apical four-chamber view, systole) demonstrating ballooning of left ventricular apical function as indicated by white arrows

Figure 2. Cardiac magnetic resonance (CMR) TruFisp cine inflow/outflow in systole (a) with ‘ballooning’ of the left ventricular mid body and apex; (b) diastole

Figure 3. Delayed viability CMR scan (a) short axis and (b) two-chamber view
After 24 hours from admission, serial daily 12-lead ECGs demonstrated marked T-wave inversion in leads V2-V6. This pattern persisted throughout the patient’s hospital stay. Transthoracic echocardiography studies demonstrated significant left ventricular impairment due to apical dyskinesia with ballooning of the apex (figure 1). She also underwent cardiac magnetic resonance (CMR) studies, which demonstrated stunned but viable left ventricular (LV) myocardium (figures 2 and 3).
Follow-up echocardiography studies demonstrated that LV function had returned to normal (figures 4 and 5).

Figure 4b. Transthoracic echocardiography three months after the initial admission (apical four-chamber view, diastole)

Figure 4a. Transthoracic echocardiography after the initial admission (apical four-chamber view, systole) demonstrating full recovery of the apex as indicated by white arrows
Clinical features and pattern of recovery was consistent with Takotsubo cardiomyopathy. This clinical entity, although rare, has been more prevalent in Japan.1 There are a few case reports describing Caucasian patients affected by this disorder.2,3 The aetiology of Takotsubo cardiomyopathy remains unclear. It is a diagnosis of exclusion. Most of the patients recover after one to two months without serious sequelae.

Figure 5. 3D echocardiography studies three months after the initial admission demonstrating full recovery of left ventricular function
None declared.
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