Primary cardiac tumours in the paediatric population

Lucio Careddu, Guido Oppido, Francesco D.imitri Petridis, Roberta Liberi, Luca Ragni, Davide Pacini, Carlo Pace Napoleone, Emanuela Angeli, Gaetano Gargiulo

Research output: Contribution to journalArticlepeer-review

27 Citations (Scopus)

Abstract

Primary cardiac tumours are relatively rare in the paediatric population, and they may occur with different signs and symptoms in foetal or post-natal life. The clinical manifestations of cardiac tumours in foetal life may include arrhythmias, congestive heart failure and hydrops. In post-natal life, cardiac tumours may cause cyanosis, respiratory distress, myocardial dysfunction, valvular insufficiency, arrhythmias, inflow or outflow tract obstructions and sudden death. Surgical treatment is essential when symptoms are present, while the role of medical therapy can merely be palliative. Results are various and related to the patients' and tumour characteristics. Primary benign heart tumours mainly have a good prognosis, while malignant neoplasms usually have a poor prognosis; in both cases, however, a strict follow-up is always mandatory in order to detect the recurrence of cardiac neoplasms after surgery.

Original languageEnglish
Pages (from-to)mmt013
JournalMultimedia manual of cardiothoracic surgery : MMCTS / European Association for Cardio-Thoracic Surgery
Volume2013
DOIs
Publication statusPublished - 2013
Externally publishedYes

Keywords

  • Cardiac tumours
  • Fibroma
  • Myxoma
  • Pericardial tumours
  • Rhabdomyoma
  • Survival

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