2例婴儿大心脏横纹肌瘤:对医疗管理的良好反应-简要报告

J. Chinawa, S. Garekar, Bhadra Y. Trivedi
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引用次数: 3

摘要

横纹肌瘤是一种罕见的儿童肿瘤,常伴有结节性硬化症。它们通常在产前诊断或作为偶然发现。第一个病例是一个2.5个月大的婴儿,在孕24周时被诊断为横纹肌瘤。心电图显示左心轴偏曲及多发房性早搏。超声心动图显示巨大的肿瘤占据了右心室腔。磁共振成像显示结节性硬化症。他开始使用依维莫司,肿瘤明显消退。第二个病例是一名8个月大的男性,他被转介给我们做心脏评估。超声心动图显示两个横纹肌瘤肿块。他也被给予依维莫司,但未能随访。横纹肌瘤是一种罕见的心脏肿瘤,对化疗反应良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Large cardiac rhabdomyoma in two infants: Good response to medical management – A brief report
Rhabdomyomas are rare tumors in children often associated with tuberous sclerosis. They are usually diagnosed during antenatal period or as an incidental finding. The first case is a 2.5-month-old child who was diagnosed to have rhabdomyomas at gestational age of 24 weeks. Electrocardiogram revealed left axis deviation and multiple premature atrial contractions. Echocardiography showed massive tumor occupying the right ventricular cavity. Tuberous sclerosis was seen on magnetic resonance imaging. He was commenced on everolimus with obvious regression of tumor. The second case is an 8-month-old male who was referred to us for cardiac evaluation. Echocardiography showed two masses of rhabdomyoma. He was also placed on everolimus but was lost to follow-up. Rhabdomyomas are rare tumors of the heart which respond well to chemotherapy.
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