2017, Number 2
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Rev Cub Med Int Emerg 2017; 16 (2)
Wolff Parkinson White Syndrome: a case report
Betancourt RGL, Betancourt BGJ, González PÁA
Language: Spanish
References: 30
Page: 48-56
PDF size: 412.64 Kb.
ABSTRACT
Background: prevalence of Wolff Parkinson White syndrome (WPWS) ranges from 0.1% to 3% being the most frequent pre excitation syndrome, and it is a common cause of rapid heart rate. WPWS, a pre excitation syndrome of the heart ventricles, is a congenital heart abnormality because of an anomalous beam, the Kent's Beak, which runs through the anterolateral part of the atrium and right ventricle (if it is on the left side it is called the Ohnell Beam).
Objective: to present a clinical case of a woman patient with the diagnosis of Wolff Parkinson White Syndrome and the antecedent of an Ebstein anomaly.
Clinical Case: a 47-year-old white female patient who had been diagnosed in childhood an Ebstein anomaly and a double excretion renal system as well as a 28-year-old daughter with Wolff Parkinson White syndrome diagnosed when she was 15 years old is presented. About 2 years ago the patient started with episodes of tachycardia, dizziness, difficulty breathing at times as well as feeling faint. A physical examination is performed along with the clinical picture and ECG, confirming the diagnosis of Wolff Parkinson White syndrome.
Conclusions: clinical manifestations accompanied by electrocardiographic classic data: PR interval less than 120 msec, wide QRS with delta wave and secondary changes of repolarization confirmed the diagnosis of a WPWS.
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