Mühler E G, Turniski-Harder V, Engelhardt W, von Bernuth G
Department of Pediatric Cardiology, RWTH Aachen, Germany.
Br Heart J. 1994 Dec;72(6):584-90. doi: 10.1136/hrt.72.6.584.
To assess the incidence, importance, and history of cardiac involvement in infants and children with tuberous sclerosis.
Prospective study; clinical examination, sector and Doppler echocardiography, standard and ambulatory electrocardiography.
A tertiary referral centre.
21 patients with tuberous sclerosis aged 1 day to 16 years (mean 6.3 years); follow up investigations were available in 14 cases (10 retrospective, 4 prospective; mean follow up 4.3 years).
Multiple cardiac rhabdomyomas in the right ventricle (11) and left ventricle (14) as well as in the right atrium (1) were present in 14/21 patients. Two of them had obstruction of the left ventricular inflow and outflow tract related to a tumour. In the remaining 7 patients, echocardiography was normal in 4 and equivocal in 3 cases. The standard electrocardiogram (n = 20) showed ventricular hypertrophy (2), ventricular pre-excitation (1), arrhythmias (2), and repolarisation disturbances (4) in 7/13 patients with rhabdomyomas but was normal in all patients with a normal or equivocal echocardiogram. The ambulatory electrocardiogram (n = 19) showed frequent premature atrial (2) and polymorphous ventricular (2) contractions. The polymorphous ventricular contractions coexisted with rhabdomyomas. No arrhythmias that needed medical treatment were found. Follow up investigations showed return to a normal standard electrocardiogram in 3 patients. Definite regression or complete disappearance of the tumour occurred in 6 infants.
Cardiac rhabdomyomas, although often present in these patients with tuberous sclerosis, caused neither major arrhythmias nor haemodynamic obstruction except in the neonatal period. The indication for operation is limited to cases with life threatening obstruction or arrhythmias refractory to medical treatment.
评估结节性硬化症患儿心脏受累的发生率、重要性及病史。
前瞻性研究;临床检查、扇形及多普勒超声心动图、标准及动态心电图检查。
一家三级转诊中心。
21例结节性硬化症患者,年龄1天至16岁(平均6.3岁);14例患者有随访调查结果(10例回顾性研究,4例前瞻性研究;平均随访4.3年)。
14/21例患者右心室(11例)、左心室(14例)及右心房(1例)存在多个心脏横纹肌瘤。其中2例患者因肿瘤导致左心室流入道和流出道梗阻。其余7例患者中,4例超声心动图正常,3例结果不明确。标准心电图(n = 20)显示,13例有横纹肌瘤的患者中7例出现心室肥厚(2例)、心室预激(1例)、心律失常(2例)及复极异常(4例),但所有超声心动图正常或结果不明确的患者心电图均正常。动态心电图(n = 19)显示频发房性早搏(2例)及多形性室性早搏(2例)。多形性室性早搏与横纹肌瘤并存。未发现需要药物治疗的心律失常。随访调查显示3例患者标准心电图恢复正常。6例婴儿的肿瘤出现明确缩小或完全消失。
心脏横纹肌瘤在这些结节性硬化症患者中虽常存在,但除新生儿期外,既未引起严重心律失常,也未导致血流动力学梗阻。手术指征仅限于有危及生命的梗阻或药物治疗无效的心律失常的病例。