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Tuberous sclerosis complex and Wolff-Parkinson-White syndrome.

机译:结节性硬化症和Wolff-Parkinson-White综合征。

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This report highlights the association between tuberous sclerosis and Wolff-Parkinson-White syndrome. Ten patients with concurrent diagnoses of Wolff-Parkinson-White syndrome and tuberous sclerosis were identified. Wolff-Parkinson-White syndrome presented early in life, nine cases being diagnosed in the first year. Eight of the 10 cases were male. In eight cases, the syndrome was associated with supraventricular tachycardias, and in nine with cardiac rhabdomyomata. One child died from cardiac failure secondary to obstruction of the left ventricular outflow tract by a rhabdomyoma. Five of nine survivors showed resolution of Wolff-Parkinson-White syndrome on follow up. The accessory pathway was localised in nine patients from surface electrocardiograms: six children had left sided pathways and three had right sided pathways.
机译:该报告强调了结节性硬化症与Wolff-Parkinson-White综合征之间的关联。确定了十例同时诊断为Wolff-Parkinson-White综合征和结节性硬化症的患者。 Wolff-Parkinson-White综合征在生命早期出现,第一年诊断出9例。 10例中有8例是男性。在八例中,该综合征与室上性心动过速有关,在九例中与心脏横纹肌瘤相关。一名儿童因横纹肌瘤阻塞左心室流出道而死于心力衰竭。九名幸存者中有五名在随访中显示出Wolff-Parkinson-White综合征的消退。根据表面心电图,该辅助途径位于9名患者中:6名儿童具有左侧途径,三名儿童具有右侧途径。

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