Primary pediatric cardiac malignancies: the SEER experience

Pediatr Surg Int. 2013 May;29(5):425-9. doi: 10.1007/s00383-013-3261-4. Epub 2013 Jan 29.

Abstract

Purpose: Pediatric cardiac malignancies are exceedingly rare. We sought to examine demographics, presentation, and outcomes for this pathology.

Methods: The SEER registry from 1973 to 2008 was queried for all patients <20 years of age with cardiac malignancies.

Results: A total of 25 pediatric patients were identified with primary cardiac malignancies, with age-adjusted incidence of 0.00686 per 100,000 United States population. Median age at diagnosis was 10 years. The majority of patients were adolescent (n = 13, 52 %), Caucasian (n = 17, 68 %) and males (n = 14, 56 %). The most common histology was soft tissue sarcoma (n = 10, 40%), followed by non-Hodgkin lymphoma and teratoma (both n = 3, 12 %). Six patients presented with distant disease. More than half of patients (n = 16, 64 %) underwent surgical resection, while four patients (16 %) underwent radiation. The mean survival time for the cohort was 47 ± 67 months, with 14 (56 %) patients dying over the study period. Lymphomas had significantly longer survival than other malignancies (108 ± 66 vs. 36 ± 66, p = 0.03), while lack of surgical treatment was associated with worse survival (p = 0.016).

Conclusions: Primary malignant cardiac tumors are exceedingly rare in pediatric patients. They are most commonly soft tissue sarcomas and lymphomas demonstrated longer survival.

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Female
  • Heart Neoplasms / epidemiology*
  • Heart Neoplasms / mortality
  • Heart Neoplasms / surgery*
  • Humans
  • Infant
  • Lymphoma, Non-Hodgkin / epidemiology
  • Lymphoma, Non-Hodgkin / mortality
  • Lymphoma, Non-Hodgkin / surgery
  • Male
  • SEER Program
  • Sarcoma / epidemiology
  • Sarcoma / mortality
  • Sarcoma / surgery
  • Teratoma / epidemiology
  • Teratoma / surgery
  • Treatment Outcome