Léiomyomatose intravasculaire utérine avec atteinte cardiaque : à propos d’un cas

Abstract

Uterine intravenous leiomyomatosis is a rare benign tumor, whose diagnosis of certainty is histological. It is characterized by its potential of intravascular extension with possibility of cardiac localisation imposing a complete surgical removal and a suitable imagery postoperatively. We report the case of a 63-year-old patient, presenting a cardiac extension complicating a LIV, by which we will discuss the diagnosis aspects, prognosis and therapeutic of this pathology.