Deeg K H, Voigt H J, Hofbeck M, Singer H, Kraus J
Cardiologic Department of the Pediatric Clinic, University of Erlangen-Nürnberg, FRG.
Pediatr Radiol. 1990;20(4):291-2. doi: 10.1007/BF02019672.
We report on a neonate with multiple cardiac rhabdomyomas, including a huge rhabdomyoma of the left ventricular posterior wall. Prenatal ultrasonography performed because of supraventricular tachycardia led to the diagnosis in the 28th week of gestation. Postnatal echocardiography confirmed the prenatal diagnosis. The tumor could not be removed surgically and the child died as a result of intractable arrhythmia at the age of 5 days. The diagnosis of multiple cardiac rhabdomyomas was confirmed by autopsy.
我们报告了一名患有多发性心脏横纹肌瘤的新生儿,其中包括左心室后壁的巨大横纹肌瘤。因室上性心动过速进行的产前超声检查在妊娠第28周时确诊。产后超声心动图证实了产前诊断。肿瘤无法手术切除,患儿在5天时因顽固性心律失常死亡。尸检证实为多发性心脏横纹肌瘤。