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患有克兰费尔特综合征的年轻成年人因窦房结功能障碍需要植入永久性起搏器。

Sinus node dysfunction requiring permanent pacemaker implantation in a young adult with Klinefelter syndrome.

作者信息

Karagöz Ahmet, Dikbaş Oğuz, Teker Erhan, Vural Aslı, Günaydın Zeki Yüksel, Bektaş Osman

机构信息

Department of Cardiology, Giresun University, Giresun, Turkey.

Department of Endocrinology, Giresun University, Giresun, Turkey.

出版信息

Am J Case Rep. 2015 Mar 6;16:136-9. doi: 10.12659/AJCR.893065.

Abstract

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.

摘要

背景

克兰费尔特综合征是男性不育最常见的遗传病因,在每500例活产中约有1例受影响。虽然伴有心脏疾病并非克兰费尔特综合征的特异性特征,但已有报道称其与二尖瓣脱垂、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等罕见相关异常情况。克兰费尔特综合征与心律失常疾病之间尚未证实存在明确关联。

病例报告

我们报告一例患有克兰费尔特综合征的年轻成年人发生窦房结功能障碍并需要植入永久起搏器的病例。该患者因心动过缓到心脏病诊所就诊。体格检查时,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失常,最低心率为33次/分钟,最高心率为154次/分钟。有3612次室性早搏、30次室性成对早搏、804次室上性早搏、7次室上性成对早搏和4次室上性心动过速发作,其中最长的为5次心跳。患者在动态心电图监测期间出现明确的头晕和恶心症状。由于现有检查结果提示存在心脏晕厥风险,因此计划进行电生理研究(EPS)。EPS结果被解释为窦房结功能障碍。进行了永久起搏器植入,此后患者症状消失。

结论

在检查患有心动过缓和/或晕厥的克兰费尔特综合征患者时应牢记这种并存情况。它很容易被误诊为癫痫,而癫痫是克兰费尔特综合征中常见遇到的异常情况。

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