[Cardiac fibroma: A rare cause of sudden child death]

Ann Pathol. 2015 Oct;35(5):445-8. doi: 10.1016/j.annpat.2015.05.004. Epub 2015 Sep 12.
[Article in French]

Abstract

We report the case of a 3-year-old child who died from the consequences of a cardio-respiratory arrest despite reanimation procedures. Echocardiography and magnetic resonance imaging (MRI) revealed a mass of the free wall of the left ventricle. Autopsy confirmed the existence of a solitary myocardial tumor, well-circumscribed, firm, with a whitish and trabeculated cut surface. Histologically, the tumor consisted of bundles of spindle-shaped and regular cells mingling with collagen and elastic fibers, insinuating themselves between myocytes in periphery. Calcifications were present. After immunohistochemistry, the cells were highlighted by anti-actin smooth muscle antibody; but they were not highlighted by anti-desmin, anti-β catenin and anti-Ki67 antibodies. The diagnosis of cardiac fibroma was made. The primary cardiac tumors of child are rare and usually benign. They are essentially represented by rhabdomyoma and fibroma. Cardiac fibroma mostly occurs during the first year of life. It can be revealed by cardiac insufficiency, arrhythmia, chest pain or sudden death.

Keywords: Cardiac tumor; Fibroma; Fibrome; Mort subite de l’enfant; Sudden child death; Tumeur cardiaque.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Calcinosis / pathology
  • Cardiomegaly / etiology
  • Child, Preschool
  • Death, Sudden, Cardiac / etiology*
  • Diagnosis, Differential
  • Fibroma / complications
  • Fibroma / diagnosis
  • Fibroma / pathology*
  • Heart Neoplasms / complications
  • Heart Neoplasms / diagnosis
  • Heart Neoplasms / pathology*
  • Humans
  • Male
  • Rhabdomyoma / diagnosis