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[家族性结节性硬化症中的心脏横纹肌瘤]

[Cardiac rhabdomyoma in familial tuberous sclerosis].

作者信息

Schneider A, Tschirky B, Arbenz U, Fanconi A

出版信息

Helv Paediatr Acta. 1986 May;41(1-2):77-85.

PMID:3721899
Abstract

Case report of a previously healthy girl who presented at the age of 9 months a paroxysmal supraventricular tachycardia. Echocardiography revealed multiple cardiac tumors. The detection of a few hardly visible unpigmented patches of skin allowed the diagnosis of tuberous sclerosis with cardiac rhabdomyomas. Computerised tomography of the brain showed typical calcifications and multiple hypodense parenchymal lesions. In the further course of the disease, progressive multifocal epilepsy and severe retardation of psychomotor development occurred, angiofibromas appeared on the face, and a suspected angiomyolipoma on renal sonography. A very mild form of this autosomal dominant phacomatosis could be detected in the patient's mother. As cardiac rhabdomyomas and tuberous sclerosis are frequently associated, investigations for both these findings with modern methods of body imaging are recommended in order to allow early diagnosis and genetic counselling.

摘要

一名既往健康的女童病例报告,该女童9个月大时出现阵发性室上性心动过速。超声心动图显示有多个心脏肿瘤。发现皮肤上有几块几乎看不见的无色素斑,从而诊断为结节性硬化症合并心脏横纹肌瘤。脑部计算机断层扫描显示典型钙化及多个低密度实质病变。在疾病的进一步发展过程中,出现了进行性多灶性癫痫和精神运动发育严重迟缓,面部出现血管纤维瘤,肾脏超声检查怀疑有血管平滑肌脂肪瘤。在患者母亲身上可检测到这种常染色体显性错构瘤病的一种非常轻微的形式。由于心脏横纹肌瘤与结节性硬化症常相关联,建议采用现代身体成像方法对这两种表现进行检查,以便早期诊断和进行遗传咨询。

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