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Multiple rhabdomyoma of the heart presenting with a congenital supraventricular tachycardia--report of case with ultrastructural study.

机译:先天性室上性心动过速的心脏多发性横纹肌瘤-超微结构研究病例报告。

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摘要

A case of congenital rhabdomyoma of the heart in a 5-month-old Korean infant is described. The patient presented with a congenital supraventricular tachyarrhymia that was detected in utero by fetal sonography. The tumor was multiple, but no obvious association with tuberous sclerosis complex was demonstrated. Microscopic examination revealed classic "spider cells" with rich glycogen content. Ultrastructurally, the cells contained numerous leptofibrils, clumped Z band material, and desmosome-like cell junctions. The case is a second documented case of cardiac rhabdomyoma in this country, and its presentation as an etiological factor of supraventricular tachycardia is a very unusual manifestation.
机译:描述了一个5个月大的韩国婴儿的心脏先天性横纹肌瘤病例。该患者表现为先天性室上性快速性心律失常,可通过胎儿超声检查在子宫内发现。肿瘤多发,但未显示与结节性硬化症的明显关联。显微镜检查发现经典的“蜘蛛细胞”具有丰富的糖原含量。在超微结构中,细胞包含大量瘦索非特,团聚的Z带材料和类似桥粒的细胞连接。该病例是该国第二例有记录的心脏横纹肌瘤病例,其表现为室上性心动过速的病因是一种非常不寻常的表现。

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