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Postnatal growth of rhabdomyoma prior to tumor regression
Wendy Whiteside1, Ziad Saba, Gregory Kurio
1Department of Cardiology, Children's Hospital & Research Center Oakland, 747 52nd Street, Oakland, CA 94609, USA.
Insights
This case study highlights a rare instance of intracardiac rhabdomyomas progressing before regression. Conservative management is encouraged even with tumor growth, especially without significant cardiovascular compromise.
Area of Science:
- Pediatric Cardiology
- Oncology
- Genetics
Background:
- Intracardiac rhabdomyomas are typically benign tumors found in infants.
- These tumors are often associated with Tuberous Sclerosis Complex.
- The natural history usually involves spontaneous postnatal regression.
Observation:
- A 1-month-old infant presented with multiple intracardiac rhabdomyomas.
- Unlike typical cases, this infant experienced significant tumor progression.
- Tumor regression was observed later, starting around 10 months of age.
Findings:
- The case demonstrates a deviation from the expected natural history of intracardiac rhabdomyomas.
- Marked tumor progression occurred before the onset of regression.
- No severe cardiovascular compromise was noted despite tumor growth.
Implications:
- This case supports conservative management strategies for intracardiac rhabdomyomas.
- Continued observation is warranted even when tumors initially progress.
- Management decisions should consider the absence of significant hemodynamic compromise.
Abstract:
We report a case of a 1-month-old infant with multiple intracardiac rhabdomyomas. In contrast to the known natural history of rhabdomyomas to show postnatal regression, this patient showed marked tumor progression prior to initiation of tumor regression at 10 months of age. In the absence of pronounced cardiovascular compromise, this finding should serve to encourage continued conservative management of rhabdomyomas despite tumor progression.
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