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Fetal-Type Rhabdomyoma of the Cheek: A Conservative Management
Angela Troisi1, Valentina Pelliccia1, Bruna Malta2
1Department of Pediatrics, Santa Maria delle Croci Hospital, 48121 Ravenna, Italy.
Extracardiac rhabdomyomas, rare benign tumors, can be managed conservatively in infants. This case shows no progression over 36 months, suggesting a viable alternative to surgery.
Area of Science:
- Pediatric Oncology
- Pathology
- Surgical Oncology
Background:
- Extracardiac rhabdomyomas are rare benign mesenchymal tumors.
- Surgical excision is the standard treatment for these tumors.
- Conservative management of fetal rhabdomyomas has not been previously reported.
Observation:
- A case of a fetal cheek rhabdomyoma in a 2-month-old boy is presented.
- The tumor was located on the left masseter muscle.
- Surgical removal was not feasible due to the patient's age and tumor size.
Findings:
- The rhabdomyoma showed no signs of spreading or progression over a 36-month follow-up period.
- Conservative management with close monitoring was successful.
- This approach avoided the risks associated with surgery in a young child.
Implications:
- Conservative management may be a viable option for select cases of fetal rhabdomyoma, particularly in the head and neck region.
- This approach can mitigate the risks of surgical complications and long-term sequelae in infants.
- Further research and case studies are warranted to establish conservative management protocols for fetal rhabdomyomas.
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