A Rare Case of Intimal Cardiac Sarcoma in an Adolescent Presenting with
Sudden Cardiogenic Shock
- Qasim Al Abri,
- Kenza Rahmouni,
- Van-Hung Nguyen,
- Christine Sabapathy,
- Claudia Renaud,
- Pierre-Luc Bernier
Kenza Rahmouni
McGill University Faculty of Medicine
Corresponding Author:kenza.rahmouni.el.idrissi@gmail.com
Author ProfileAbstract
Primary cardiac tumors are extremely rare and they most commonly occur
in adults. The majority of these neoplasms are benign and, in children,
rhabdomyomas, fibromas and teratomas represent the most prevalent
subtypes. Among the malignant primary cardiac tumors, sarcomas are the
most common. In this case report, we present the first pediatric case of
a primary cardiac intimal sarcoma, a histological subtype never
previously reported in the pediatric population. Our patient is a
16-year-old who presented with severe cardiogenic shock and arrhythmias
and underwent urgent surgical resection of his cardiac mass.