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首页> 外文期刊>Archives of disease in childhood >Ganglioneuroblastoma presenting as dilated cardiomyopathy.
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Ganglioneuroblastoma presenting as dilated cardiomyopathy.

机译：表现为扩张型心肌病的神经节神经母细胞瘤。

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We report an unusual presentation of ganglioneuroblastoma with features of dilated cardiomyopathy in a 22 month old girl. She was admitted with cardiomegaly; during echocardiography a suspicious abdominal mass was detected by chance. Further imaging studies, including abdominal ultrasonography and spiral computed tomography, revealed a solid mass originating in the right adrenal gland. Metabolic studies and pathological findings were compatible with ganglioneuroblastoma. Following tumour removal and supportive therapy for cardiomyopathy, her clinical condition and laboratory findings improved. Although ganglioneuroblastoma with features of dilated cardiomyopathy is rare, because neurogenic tumours may be involved in its development, measurement of catecholamines in children with dilated cardiomyopathy is strongly recommended.
机译：我们在22个月大的女孩中报告了神经节神经母细胞瘤的异常表现，并伴有扩张型心肌病。她因心脏肥大而入院;在超声心动图检查中，偶然发现可疑的腹部肿块。进一步的影像学研究（包括腹部超声检查和螺旋计算机断层扫描）显示出源于右肾上腺的实性肿块。代谢研究和病理结果与神经节神经母细胞瘤相容。在去除肿瘤和支持疗法治疗心肌病后，她的临床状况和实验室检查结果得到改善。尽管具有扩张型心肌病特征的神经节神经母细胞瘤很少见，但由于神经源性肿瘤可能参与了其发展，因此强烈建议对扩张型心肌病儿童进行儿茶酚胺测定。

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