Rhabdomyosarcoma-RMS
Rhabdomyosarcoma is a malignant tumor of skeletal muscle cells, commonly seen in children and adolescents.
Symptoms depend on tumor location and may include swelling, pain, or functional limitation. Early diagnosis and treatment are crucial. Management typically involves surgery to remove the tumor, chemotherapy to target residual cancer cells, and radiotherapy in select cases.
Causes and Risk Factors of Rhabdomyosarcoma
Exact cause is unknown, but genetic and environmental factors may play a role.
- Genetic predisposition: Mutations in genes regulating muscle cell growth
- Family history of cancer
- Environmental exposures in rare cases
Symptoms and Clinical Features
Symptoms vary by tumor site:
- Painless or painful mass or swelling
- Functional limitation or movement restriction
- Respiratory or gastrointestinal symptoms: If tumor compresses nearby organs
Treatment Options for Rhabdomyosarcoma
Treatment is multimodal to maximize cure and minimize recurrence.
- Surgical resection: Complete removal of tumor when feasible
- Chemotherapy for systemic control
- Radiotherapy: Target residual tumor or high-risk areas
Why Choose Us for Rhabdomyosarcoma
CureU Healthcare provides expert pediatric oncology surgeons, advanced imaging, chemotherapy protocols, and compassionate care for children.
Conclusion
Timely diagnosis and multimodal treatment improve outcomes in rhabdomyosarcoma. CureU Healthcare ensures comprehensive pediatric oncology care.
