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A Rare Case of Intimal Cardiac Sarcoma in an Adolescent Presenting with Sudden Cardiogenic Shock
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  • Qasim Al Abri,
  • Kenza Rahmouni,
  • Van-Hung Nguyen,
  • Christine Sabapathy,
  • Claudia Renaud,
  • Pierre-Luc Bernier
Qasim Al Abri
Montreal Children's Hospital
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Kenza Rahmouni
McGill University Faculty of Medicine

Corresponding Author:kenza.rahmouni.el.idrissi@gmail.com

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Van-Hung Nguyen
Montreal Children's Hospital
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Christine Sabapathy
Montreal Children's Hospital
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Claudia Renaud
Montreal Children's Hospital
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Pierre-Luc Bernier
Montreal Children's Hospital
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Abstract

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.