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Title: Left atrial mass 16 years after radiation therapy for mediastinal neuroblastoma

Journal Article · · Pediatr. Cardiol.; (United States)
DOI:https://doi.org/10.1007/BF02427541· OSTI ID:5441220

Tumors involving the heart during childhood are rare. However, neuroblastoma, a common pediatric malignancy, has been described to involve the cardiovascular system in 3%-12% of patients dying with this tumor. Rarely is such involvement diagnosed ante mortem and never, to our knowledge, has a benign cardiac tumor been reported to present in childhood after successful eradication of neuroblastoma. We describe the identification and surgical resection of a nodular, hypertrophied, calcified, pedunculated left atrial mass in a 16-year-old boy who was complaining of exercise-associated presyncope and headaches 16 years after irradiation and chemotherapy for mediastinal neuroblastoma.

Research Organization:
Mayo Clinic, Rochester, MN (USA)
OSTI ID:
5441220
Journal Information:
Pediatr. Cardiol.; (United States), Vol. 8:4
Country of Publication:
United States
Language:
English