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Sinus Node Dysfunction Requiring Permanent Pacemaker Implantation in a Young Adult with Klinefelter Syndrome

机译:患有Klinefelter综合征的年轻成年人永久性起搏器植入的窦房结功能障碍

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Patient: Male, 22 Final Diagnosis: Sinus node dysfunction Symptoms: Bradycardia ? lassitude Medication: — Clinical Procedure: Pacemaker implantation Specialty: Cardiology Objective: Unusual clinical course Background: Klinefelter syndrome is the most common genetic cause of male infertility and affects approximately 1 in 500 live births. Although accompanying cardiac disorder is not a specific feature of Klinefelter syndrome, rarely associated anomalies such as mitral valve prolapse, atrial septal defect, ventricular septal defect, tetralogy of Fallot, patent ductus arteriosus, and hypertrophic obstructive cardiomyopathy have been reported. A clear association between Klinefelter syndrome and arrhythmic disorders has not yet been demonstrated. Case Report: We report a case of a sinus node dysfunction that required permanent pacemaker implantation in a young adult with Klinefelter syndrome. The patient was consulted to cardiology clinic due to bradycardia. On physical examination, no cardiac abnormality was detected except for bradycardia. Holter results showed sinus arrhythmia with a minimum heart rate of 33 bpm and maximum of 154 Bpm. There were 3612 ventricular premature beats, 30 ventricular pairs, 804 supraventricular premature beats, 7 supraventricular pairs, and 4 supraventricular runs, the longest of which was 5 beats. The patient had defined dizziness and nausea during Holter monitoring. Electrophysiological study (EPS) was planned because existing findings indicated risk of cardiac syncope. Findings of EPS were interpreted as sinus node dysfunction. A permanent pacemaker implantation was performed and the patient has been free of symptoms since. Conclusions: This concomitance should be kept in mind when examining patients with Klinefelter syndrome with bradycardia and/or syncope. It is easily mistaken for epilepsy, which is a commonly encountered abnormality in Klinefelter syndrome.
机译:患者:男性,22岁最终诊断:窦房结功能障碍症状:心动过缓?轻度药物:—临床步骤:起搏器植入专长:心脏病学目的:异常的临床过程背景:克莱氏综合征是男性不育的最常见遗传原因,大约每500例活产中就有1例。尽管伴发的心脏疾病不是Klinefelter综合征的特征,但很少有相关异常,如二尖瓣脱垂,房间隔缺损,室间隔缺损,法洛四联症,动脉导管未闭和肥厚性梗阻性心肌病。 Klinefelter综合征与心律失常之间没有明确的关联。病例报告:我们报告了一例窦房结功能不全的病例,该病例需要在患有Klinefelter综合征的年轻成年人中永久植入起搏器。由于心动过缓,该患者被咨询了心脏病诊所。体格检查中,除心动过缓外,未发现心脏异常。动态心电图结果显示窦性心律不齐,最小心律为33 bpm,最大心律为154 Bpm。室性早搏3612次,心室对30次,室上早搏804次,室上对7次,室上运动4次,最长为5次。在动态心电图监测中,患者出现头晕和恶心。之所以计划进行电生理研究(EPS),是因为现有发现表明存在心脏晕厥的风险。 EPS的发现被解释为窦房结功能障碍。自从开始永久性起搏器植入后,患者就没有症状了。结论:检查伴有心动过缓和/或晕厥的Klinefelter综合征患者时应牢记这一点。它很容易被误认为是癫痫病,这是克莱恩费尔特综合征中常见的异常现象。

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