Complete Resection of a Right-Sided Interventricular Septal Fibroma

Dante Picarelli1, Ruben Leone1, José L Surraco1

  • 11 Division of Pediatric Cardiac Surgery and Pediatric Cardiology, Integral Cardiac Institut, Montevideo, Uruguay.

Insights

A large cardiac fibroma in a 15-month-old infant caused dangerous arrhythmias and outflow tract obstruction. Surgical resection was successful, confirming the ventricular fibroma diagnosis and resolving the life-threatening condition.

Area of Science:

  • Pediatric Cardiology
  • Cardiac Oncology
  • Congenital Heart Disease

Background:

  • Cardiac fibromas are rare benign tumors in infants and children.
  • Intracardiac masses can lead to significant hemodynamic compromise and arrhythmias.
  • Early diagnosis and intervention are crucial for managing pediatric cardiac tumors.

Observation:

  • A 15-month-old infant presented with a systolic cardiac murmur and developed nonsustained ventricular tachycardia.
  • Transthoracic echocardiography and magnetic resonance imaging revealed a large intracardiac mass causing interventricular septum widening and right ventricular outflow tract obstruction.
  • The mass was suspected to be a cardiac fibroma due to the risk of life-threatening arrhythmias.

Findings:

  • Surgical resection of the intracardiac mass was performed despite its challenging location.
  • Complete tumor removal was achieved successfully.
  • Microscopic examination confirmed the diagnosis of ventricular fibroma.

Implications:

  • This case highlights the importance of prompt diagnosis and surgical management of cardiac fibromas in infants.
  • Successful resection can prevent life-threatening arrhythmias and improve cardiac function.
  • Pediatric cardiac surgeons should be prepared for complex tumor resections in challenging anatomical locations.

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