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When Chemotherapy Is Not Enough-Management of Prostatic Embryonal Rhabdomyosarcoma in an Infant
Christina P Carpenter1, Joseph M Gleason1
1Le Bonheur Children's Hospital, Memphis, TN; University of Tennessee Health Science Center, Memphis, TN; St. Jude Children's Research Hospital, Memphis, TN.
Insights
This case study highlights a novel surgical approach for a rare infant embryonal rhabdomyosarcoma. An individualized treatment plan led to successful disease eradication in a young patient.
Area of Science:
- Pediatric Oncology
- Surgical Innovation
- Pediatric Urology
Background:
- Embryonal rhabdomyosarcoma is a rare pediatric malignancy.
- Left hydroureteronephrosis can be a complication of pelvic tumors.
- Standard treatment protocols may require adaptation for complex cases.
Abstract:
A baby boy was diagnosed with embryonal rhabdomyosarcoma causing left hydroureteronephrosis. A loop ureterostomy was performed, and the infant was treated per the RMS13 protocol. After 3 months of chemotherapy, the infant's tumor burden increased, and he underwent radical cystoprostatectomy and right-to-left transureteroureterostomy (end-to-end fashion utilizing the distal limb of his ureterostomy). This innovative method was utilized because the infant's tumor burden was too large to be treated effectively and safely with radiation. One year later, the infant has no evidence of disease. This demonstrates that optimal management of rhabdomyosarcoma is still unknown; therefore, each child warrants an individualized approach for optimal outcomes.
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