Case report shows hypertensive cardiomyopathy caused by catecholamines in a child, highlighting treatment importance.
Unlike pheochromocytomas, neuroblastomas—which are the most common pediatric extracranial solid tumors—are rarely associated with cardiomyopathy and heart failure due to hypertension. We report the case of a 3-year-old girl with growth failure who had hypertensive cardiomyopathy caused by excessive epinephrine and norepinephrine production from a ganglioneuroblastoma. Circulation improved with alpha-blockers and other medications, which enabled partial tumor resection. Histopathologic analysis confirmed ganglioneuroblastoma. Four courses of James' therapy did not lead to tumor shrinkage; subtotal resection was required, which reduced catecholamine levels. This case underscores the importance of multidisciplinary treatment for hypertensive cardiomyopathy due to excess neuroblastoma-related catecholamines.
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Shimizu et al. (2026) studied this question.
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