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Cardiac Inflammatory Myofibroblastic Tumor Causing Pulmonary Artery Obstruction: A Rare Case Report
Kaan Yildiz1, Halise Zeynep Genc1, Mustafa Kir1
1Departments of Pediatric Cardiology.
Journal of Pediatric Hematology/Oncology
|December 4, 2020
Summary
A rare cardiac inflammatory myofibroblastic tumor (IMT) was found in a 5-year-old boy. Successful surgical removal of the pulmonary valve mass prevented recurrence, highlighting early diagnosis and intervention for this uncommon heart tumor.
Area of Science:
- Cardiology
- Pediatric Oncology
- Pathology
Background:
- Inflammatory myofibroblastic tumor (IMT) is a rare soft tissue neoplasm.
- Cardiac IMT typically presents as an endocardial mass in the right heart of pediatric patients.
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