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Updated: Jul 17, 2026
06:29
Cardiac Magnetic Resonance for the Evaluation of Suspected Cardiac Thrombus: Conventional and Emerging Techniques
Published on: June 11, 2019
Intracardiac inflammatory myofibroblastic tumor: a unique presentation
Kenneth A Murdison1, Stuart Septimus, Robert E Garola
1Nemours Cardiac Center, A I duPont Hospital for Children, Wilmington, DE 19803, USA. kmurdiso@nemours.org
Summary
Pediatric cardiac tumors are rare, often appearing in infancy as rhabdomyomas. This case highlights a unique, rarely documented intracardiac tumor found in an asymptomatic 7-year-old child.
Area of Science:
- Pediatric cardiology
- Pediatric oncology
- Cardiovascular pathology
Background:
- Cardiac tumors are uncommon in children, with most diagnoses occurring in infancy.
- Rhabdomyomas represent the most frequent type of pediatric cardiac tumor.
- Early detection and accurate diagnosis are crucial for managing pediatric cardiac conditions.
Observation:
- A rare intracardiac tumor was identified in a 7-year-old child.
- The child presented with no symptoms, indicating an incidental finding.
- This case represents a unique occurrence of a seldom-documented tumor type.
Findings:
- The tumor's specific histology and location are detailed in the full study.
- Diagnostic imaging and pathological analysis confirmed the tumor's nature.
- The asymptomatic presentation underscores the importance of thorough cardiac evaluations.
Implications:
- This case expands the understanding of rare cardiac tumors in pediatric populations.
- It may prompt further research into the etiology and management of such rare tumors.
- Clinicians should consider a broad differential diagnosis for intracardiac masses in children, even in asymptomatic cases.
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