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Rhabdomyosarcoma Treatment Cost in India
Rhabdomyosarcoma is a rare type of cancer that primarily affects children and adolescents. It can happen anywhere in the body, but it most commonly occurs in the head and neck, arms and legs, and urinary and reproductive organs. Surgery, chemotherapy, radiation, and supportive care are all options for rhabdomyosarcoma treatment in India. Several factors can have an impact on survival. Patient outcomes vary considerably, with 5-year survival rates ranging from 35% to 95% depending on the type of RMS involved, so an accurate diagnosis is essential for effective treatment and management. Because of the heterogeneity of Rhabdomyosarcoma tumors and the…
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    What Are the Treatment Options for Rhabdomyosarcoma? Your child’s medical team will recommend a combination of treatments based on the following factors: Rhabdomyosarcoma stage and type Potential side effects The individual’s overall health and preferences. The following are the major types of treatment for rhabdomyosarcoma in India: Chemotherapy: It involves…
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    The Most Important Frequently Asked Questions

    Q: How Long Is the Treatment for Rhabdomyosarcoma?

    A: The duration of treatment typically ranges from 6 months to a year. Some drugs can be taken orally, but the majority are administered intravenously (injected into a vein). RMS patients are treated with a combination of chemotherapy drugs.

    Q: Can Rhabdomyosarcoma Be Cured Permanently with Surgery?

    A: Childhood rhabdomyosarcoma is treated with surgery (the cancer is removed during the operation). A procedure known as wide local excision is frequently used. Wide local excision is the removal of the tumor as well as some of the surrounding tissue, including the lymph nodes. A second surgery may be required to completely remove cancer.

    Q: What Causes Childhood Rhabdomyosarcoma?

    A: The precise cause of rhabdomyosarcoma is unknown. Changes in the genetic material (DNA) in cells can cause the cells to become cancerous.

    Q: Does Rhabdomyosarcoma Come Back?

    A: Although current treatment achieves complete remission in more than 90% of children with nonmetastatic rhabdomyosarcoma (RMS), up to one-third of them experience recurrence. Survival rates in patients who develop recurrences are not always poor; thus, prognostic factors are required to tailor salvage treatment.

    Q: Is Rhabdomyosarcoma a Fast-Growing Tumor?

    A: Rhabdomyosarcoma cells are frequently fast-growing and can spread (metastasize) to other parts of the body. The most common type of soft-tissue cancer in children is rhabdomyosarcoma. It can affect children of any age, but the majority of cases occur in children aged 2 to 6 years old and 15 to 19 years old.

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