Department of Pediatrics, Hacettepe University İhsan Doğramacı Children's Hospital, Ankara.
Department of Pediatric Cardiology, Hacettepe University İhsan Doğramacı Children's Hospital, Ankara.
Turk J Pediatr. 2023;65(3):479-488. doi: 10.24953/turkjped.2022.922.
Primary cardiac tumors are extremely rare. Cardiac rhabdomyoma is the most common primary cardiac tumor. 50-80% of solitary rhabdomyomas and all multiple rhabdomyomas are associated with tuberous sclerosis complex. Due to spontaneous regression, surgery is necessary only in severe hemodynamic compromise and persistent arrhythmias. Everolimus, a mechanistic target of rapamycin (mTOR) inhibitor, can be used in the treatment of rhabdomyomas seen in tuberous sclerosis complex. We aimed to evaluate the clinical progression of rhabdomyomas followed-up in our center between the years 2014-2019 and evaluate the efficacy and safety of everolimus treatment on tumor regression.
Clinical features, prenatal diagnosis, clinical findings, tuberous sclerosis complex presence, treatment and follow-up results were evaluated retrospectively.
Among 56 children with primary cardiac tumors, 47 were diagnosed as rhabdomyomas, 28/47 patients (59.6%) had prenatal diagnosis, 85.1% were diagnosed before one year of age and 42/47 patients (89.3%) were asymptomatic. Multiple rhabdomyomas were present in 51% and median diameter of tumors was 16mm (4.5 - 52 mm). In 29/47 patients (61.7%) no medical or surgical treatment were necessary while 34% of these had spontaneous regression. Surgery was necessary in 6/47 patients (12.7%). Everolimus was used in 14/47 patients (29.8%). Indications were seizures (2 patients) and cardiac dysfunction (12 patients). Regression in size of rhabdomyomas was achieved in 10/12 patients (83%). Although, in the long-term, the amount of tumor mass shrinkage was not significantly different between patients who received everolimus and untreated patients (p=0.139), the rate of mass reduction was 12.4 times higher in patients who received everolimus. Leukopenia was not detected in any of the patients, but, hyperlipidemia was noted in 3/14 patients (21.4%).
According to our results, everolimus accelerates tumor mass reduction, but not amount of mass regression in the long term. Everolimus may be considered for treatment of rhabdomyomas which cause hemodynamic compromise or life-threatening arrhythmias before surgical intervention.
原发性心脏肿瘤极为罕见。心脏横纹肌瘤是最常见的原发性心脏肿瘤。50-80%的孤立性横纹肌瘤和所有多发性横纹肌瘤均与结节性硬化症复合征相关。由于横纹肌瘤存在自发消退的可能性,因此仅在严重的血液动力学受损和持续性心律失常的情况下才需要手术。依维莫司是一种雷帕霉素(mTOR)的作用机制靶点抑制剂,可用于治疗结节性硬化症复合征相关的横纹肌瘤。我们旨在评估 2014 年至 2019 年间在我们中心随访的横纹肌瘤的临床进展,并评估依维莫司治疗对肿瘤消退的疗效和安全性。
回顾性评估临床特征、产前诊断、临床发现、结节性硬化症复合征存在、治疗和随访结果。
在 56 例原发性心脏肿瘤患儿中,47 例诊断为横纹肌瘤,28/47 例(59.6%)存在产前诊断,85.1%在 1 岁前诊断,42/47 例(89.3%)无症状。多发性横纹肌瘤占 51%,肿瘤直径中位数为 16mm(4.5-52mm)。29/47 例(61.7%)患儿无需药物或手术治疗,其中 34%存在自发性消退。6/47 例(12.7%)患儿需要手术。14/47 例(29.8%)患儿使用依维莫司。用药指征为癫痫发作(2 例)和心功能障碍(12 例)。12 例患者中,横纹肌瘤的大小得到了消退。尽管长期来看,接受依维莫司治疗和未接受治疗的患者肿瘤体积缩小程度无显著差异(p=0.139),但接受依维莫司治疗的患者肿瘤体积减少的速度要快 12.4 倍。所有患者均未出现白细胞减少症,但有 3/14 例(21.4%)患者出现高脂血症。
根据我们的结果,依维莫司可加速肿瘤质量的减少,但长期来看并不会增加肿瘤体积的消退程度。对于可能导致血液动力学受损或危及生命的心律失常的横纹肌瘤,在手术干预之前,可考虑使用依维莫司进行治疗。