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The cost of rhabdomyosarcoma treatment in India starts from USD 5500. we offer a treatment strategy that fits your budget. Apart, we assist patients with obtaining travel authorizations, medical visas, and a multitude of other things.
The overall cost of rhabdomyosarcoma treatment in India is quite low as compared to other developed countries like the USA and the UK. Major advances in the treatment of rhabdomyosarcoma in India have significantly improved outcomes. People must be monitored for the rest of its life for the potential long-term effects of intensive chemotherapy and radiation.
Rhabdomyosarcoma is one of the cancer types that affect the muscles. It is most prevalent in children and adolescents. The disease begins in mesenchymal cells, which are muscle-forming cells. The cells in rhabdomyosarcoma change and grow out of control, resulting in one or more tumors. Rhabdomyosarcoma can develop anywhere in the body, but it is most commonly found in the following areas:
Rhabdomyosarcoma is rare cancer. In the world, only about 700 people are diagnosed each year. The vast majority of them are children or adolescents. Rhabdomyosarcomas can be classified as follows:
The type of rhabdomyosarcoma, where it begins, tumor size, and whether cancer has spread all influence the prognosis and treatment decisions. Surgery, chemotherapy, and radiation therapy are commonly used in treatment.
The signs and symptoms of rhabdomyosarcoma are determined by the location of cancer. For an instance, If the cancer is in the head or neck, signs and symptoms may include, among others:
If the cancer is in the urinary or reproductive system, the following signs and symptoms may occur:
Signs and symptoms of cancer in the arms or legs may include, but are not limited to:
It is unclear what actually causes rhabdomyosarcoma.
Doctors know that rhabdomyosarcoma develops when a cell’s DNA changes. The DNA of a cell contains the instructions that tell it what to do. The changes instruct the cell to multiply quickly and to continue to live when healthy cells would normally die. As a result, a mass (tumor) of abnormal cells forms, which can invade and destroy healthy body tissue. The abnormal cells can separate and spread (metastasize) throughout the body.
Risk Factors –
The following factors may increase the risk of rhabdomyosarcoma:
Rhabdomyosarcoma is diagnosed typically through a physical exam to better understand the symptoms you or your child are experiencing. Other tests and procedures may be recommended based on the findings.
Your doctor may recommend one or more imaging tests to investigate symptoms, detect cancer, and identify signs of cancer spread.
Imaging tests may include the following:
A biopsy procedure is used to collect a sample of suspicious cells for testing in the laboratory. Tests can determine whether the cells are cancerous and the type of cancer.
The following biopsy procedures are used to diagnose rhabdomyosarcoma:
Needle Biopsy: The doctor guides a thin needle through the skin into the tumor. The needle is used to extract small pieces of tumor tissue.
Surgical Biopsy: The doctor makes an incision in the skin and removes the entire tumor (excisional biopsy) or a portion of the tumor (partial biopsy) (incisional biopsy).
Your child’s medical team will recommend a combination of treatments based on the following factors:
The following are the major types of treatment for rhabdomyosarcoma in India:
The cost of rhabdomyosarcoma treatment in India can be determined by several factors, including:
Approximately 70% of people with rhabdomyosarcoma live for five years or longer. However, the outlook varies greatly depending on a number of factors, including:
Rhabdomyosarcoma can sometimes be cured with treatments. This is known as remission, and it means that cancer can no longer be detected. Although remission is often permanent, rhabdomyosarcoma can reoccur. This is known as recurrence. Recurrence can occur in the same or a different part of the body.
Your healthcare team will categorize the disease into a risk group in order to predict the likelihood of recurrence of rhabdomyosarcoma. The risk category (low, intermediate, or high) will also assist the healthcare team in deciding on the best treatment or combination of treatments. If rhabdomyosarcoma recurs, your child’s medical team will conduct additional tests and recommend additional treatments.
Childhood rhabdomyosarcoma is, thankfully, extremely rare. Your child’s healthcare team can determine whether or not he or she has this type of cancer and, if so, what stage it is. The team will collaborate with you to develop a treatment strategy and will provide support to help your family cope.
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