Infantile Ganglioneuroblastoma Causing Growth Failure and Hypertensive Cardiomyopathy From Excessive Catecholamine Production

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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Publication Details

Journal
Journal of Pediatric Hematology/Oncology
Published
2026-03-20
DOI
https://doi.org/10.1097/mph.0000000000003192
Primary Topic
Neuroblastoma Research and Treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

Infantile Ganglioneuroblastoma Causing Growth Failure and Hypertensive Cardiomyopathy From Excessive Catecholamine Production

Tomohei Nakao, Keisuke Suzuki, Takashi Fukushima, Yujiro Tanaka et al.
Journal of Pediatric Hematology/Oncology
Neuroblastoma Research and Treatments
article

Infantile Ganglioneuroblastoma Causing Growth Failure and Hypertensive Cardiomyopathy From Excessive Catecholamine Production

Tomohei Nakao, Keisuke Suzuki, Takashi Fukushima, Yujiro Tanaka, Kouichi Toda, Atsuhiko Ohta, Haruka Shimizu, Ryuhei Tanaka, Yuki Shimizu
article en

Abstract

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.

Journal of Pediatric Hematology/Oncology
Saitama Medical University (JP)
Good health and well-being
Openalex Percentile: Top 12%
Neuroblastoma Research and Treatments
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