Freymann R, Oelert H, Kallfelz H C
Z Kardiol. 1977 Jan;66(1):35-8.
An unusual case of cardiac rhabdomyomatosis associated with a ventricular septal defect without signs of tuberous sclerosis is described. On 3 different angiocardiographies the region of the tumor seemed to be a right ventricular aneurysm. The tumor was identified as such only on operation and its nature defined histologically. Subtotal excision of the tumor and closure of the large ventriccular septal defect and debanding (pulmonary banding at the age of 8 month) was successfully undertaken at the age of 10 years.
本文描述了一例罕见的心脏横纹肌瘤病，该病例伴有室间隔缺损，且无结节性硬化症的体征。在3次不同的心血管造影检查中，肿瘤区域似乎是右心室动脉瘤。肿瘤仅在手术时被确诊，并通过组织学确定其性质。在患儿10岁时，成功进行了肿瘤次全切除、大型室间隔缺损修补及去带术（8个月大时进行的肺动脉束带术）。
