Abstract
Introduction. Sustained monomorphic ventricular tachycardia (SMVT) is a rare,
underdiagnosed pathology, with a very poor prognosis. Along with ventricular
fibrillation, SMVT is responsible for nearly all of the arrhythmic sudden
cardiac death (SCD). The most common cause of ventricular tachycardia is
ischemic heart disease, but there are many other reasons, among which are:
arrhythmogenic right ventricular cardiomyopathy (ARVD) and myocardial
bridging phenomenon. Treatment options include a hybrid approach consisting
of antiarrhythmic drugs, catheter ablation and implantable cardioverter
defibrillators (ICD). Case report. We present a case of 46-year old man,
military officer, who experienced chest pain, palpitations and nausea during
regularly physical activity at home. Due to the symptoms described, he
examined immediately and diagnosed sustained monomorphic ventricular
tachycardia. Shortly after the diagnosis, he lost consciousness, and
successfully resuscitated. A complete non-invasive and invasive cardiology
examination performed and it revealed that the patient had stable coronary
disease, a muscle bridge on the LAD, and arrhythmogenic right ventricular
cardiomyopathy suspected after transthoracic echocardiography and heart MRI.
Genetic testing for ARVD was negative, but according to the Heart Rhythm
Society (HRS) expert consensus criteria, we had enough for a definitive
diagnosis. Conclusion. SMVT is the most common cause of sudden cardiac
death. It is of inestimable importance to carry out a detailed examination
and determine the immediate cause of the arrhythmia and the right therapy,
which for these patients is a life-saving form of treatment. Therapy
includes medications, electrophysiology, or ICD, or a combination of these
treatment approaches.
Publisher
National Library of Serbia