Hanke J, Doetsch N, Zerkowski H R, Reidemeister J C, Schramm G
Dtsch Med Wochenschr. 1982 Jan 15;107(2):55-9. doi: 10.1055/s-2008-1069871.
A teratoma of the cardiac skeleton, a rhabdomyoma of the right ventricle and an intramural fibroma in the left ventricle were observed in three children, aged eight weeks, eight months and eight years, respectively. Atrial myxoma was found in a 42-year-old and a 49-year-old patient. History and symptoms showed no particular common features in the various patients, merely signs of flow obstruction in four of the five patients. Amongst specific cardiological diagnostic methods only angiocardiography was reliable in the demonstration of intra- or paracardiac space-occupying lesions. All five patients were successfully operated on under cardiopulmonary bypass. The surgical technique varied according to localisation, extent of the tumour and its site in relation to essential cardiac structures. Follow-up examination indicated that the patients were free of symptoms and recurrence.
分别在一名8周、一名8个月和一名8岁的儿童中观察到心脏骨骼畸胎瘤、右心室横纹肌瘤和左心室壁内纤维瘤。在一名42岁和一名49岁的患者中发现心房黏液瘤。病史和症状在不同患者中没有特别的共同特征,仅5名患者中有4名有血流梗阻迹象。在特定的心脏诊断方法中,只有心血管造影术在显示心内或心旁占位性病变方面是可靠的。所有5名患者均在体外循环下成功进行了手术。手术技术根据肿瘤的位置、范围及其与心脏重要结构的关系而有所不同。随访检查表明患者无症状且未复发。