Cancerous tumour of the connective tissues is termed as Sarcoma. Normal connective tissue includes nerves, bones, fat, blood vessels, muscles, and cartilage. Sarcoma is divided into two main groups- soft tissue sarcomas & bone sarcomas.
- Soft Tissue sarcoma (STS):
Soft Tissue Sarcoma is a rare form of cancer. It comprises of approximately 1% of all cancers diagnosed. STS can occur in the muscles, fat, fibrous tissues and synovial tissues (tissues around joints), blood vessels, tendons. Approximately 40 % occur in the legs usually at or above the knee. 30% in the shoulders, chest, abdomen, or hips, 10% develop in the hands and arms, another 20% in the head and neck. Soft tissue sarcoma’s can invade and spread to nearby area to develop secondary cancer or metastasis. They are very elastic and usually diagnosed when tumor is of large size.
- Bone sarcoma:
Second group of sarcoma is bone sarcoma or also called as the bone cancer. It could be primary when it start within the bone or metastatic when it is spread to bones from other parts of the body. Bone consist of three types of tissue i.e. compact tissue which is outer hard portion of the bone, cancellous tissue which is spongy tissue inside the bone containing the bone marrow, and subchondral tissue which is smooth bone tissue of joints. There are three types of bone sarcoma: Osteosarcoma, Ewing’s sarcoma and chondrosarcoma.
- OSTEOSARCOMA(Osteogenic sarcoma):
The most common bone sarcoma is osteosarcoma, which is most likely to develop in large bones i.e. the shin bone, thigh bone or upper arm. Highest incidence of osteosarcoma is in children as it occurs in growing bones.
- EWING’S SARCOMA
Ewing’s sarcoma is a rare form of bone sarcoma which is usually seen in teenagers. Most Ewing tumors occur in the bones. The most common sites are pelvis (hip bones), chest wall (such as the ribs or shoulder blades), mainly in the middle of the long bones.
Chondrosarcoma is a cancer that involves the cartilage (a tough, flexible material that covers the joints of the bone). Chondrosarcoma usually develops in adults aged between 30 and 60. It mostly affects the pelvis, thigh bone, upper arm bone, shoulder blade (scapula) and the ribs. It is usually resistant to chemotherapy and radiation therapy.
As soft tissue sarcoma is a very rare kind of cancer. Exact cause of soft tissue sarcoma is not defined. But still there are some risk factors which are found to be associated with high probability of getting soft tissue sarcoma.
- Therapeutic radiation: Exposure to radiations for treatment of cancer can make a person prone to develop soft tissue sarcoma later in life at same place of exposure.
- Environmental radiation: Exposure to radiations like radon gas is considered as high risk factor to develop STS.
- Genetic conditions: Some rare genetic conditions like Neurofibromatosis, Li-Fraumeni syndrome, Retinoblastoma can increase the cancer risk.
- Chemicals: Chemicals like Vinyl Chloride which is used in Plastic industries is thought to increase the risk of liver sarcoma.
- Injuries: Though not proved, but many people with bone cancer encountered bone injuries during some time of their life.
- Other factors: Paget disease is a benign (non-cancerous) but pre-cancerous condition that affects one or more bones. It results in formation of abnormal bone tissue. Affected bones are heavy, thick, and brittle. They are weaker than normal bones and more likely to fracture. Bone cancer (usually osteosarcoma) develops in about 1% of those with Paget disease.
Symptoms of bone cancer can vary depending on the size and location of the tumor.
- Pain in the affected bone is the most common complaint of patients with sarcoma. Initially the pain is of less intensity but gradually it increases. It increases with physical activity and the person might limp if a leg is involved.
- Cancers in the bones of the neck can cause a lump in the back of the throat that can lead to trouble swallowing or make it hard to breathe. Swelling in the area of the pain may not occur until it is large in size. It might be possible to feel a lump or mass depending on the location of the tumor.
- Bone cancer can weaken the bone it develops in and increase risk of bone fractures. People with fracture due to bone cancer come up with sudden pain or difficulty in walking.
- Cancer in the bones of the spine can press on nerves, leading to numbness and tingling or even weakness.
- X-rays: Most bone cancers show up on x-rays of the bone. The bone at the site of the cancer may appear “ragged” instead of solid. The cancer can also appear as a hole in the bone. A chest x-ray is often done to see if bone cancer has spread to the lungs.
- Magnetic resonance imaging (MRI) scans: MRI scans are often the best test for outlining a bone tumor.
- Computed tomography (CT) scans: CT scans are helpful in staging cancer. They help find out if the bone cancer has spread into the lungs, liver, or other organs. These scans also show the lymph nodes and distant organs where metastatic cancer might be present.
- PET scans: They are useful in looking for cancer throughout the body. It can sometimes help tell if a tumor is cancerous or benign.
- Biopsy: If cancer is present, the biopsy can tell the doctor if it is a primary bone cancer or cancer that started somewhere else and has spread to the bones (metastasis).
The only way to prevent sarcoma is to avoid exposure to chemicals like vinyl chloride and other known factors that can be avoided.
Cancer healer therapy helps to treat all types of sarcoma i.e. soft tissue sarcoma and bone sarcoma. Treatment works at immune level to enhance and boost the immune system so that the body itself starts fighting against the cancer cells to control and reduce their growth. Medicines can be given in cases where patients have already undergone surgery, to prevent the further growth of tumour or to prevent chances of recurrence. There are different lines of treatment for different types of sarcoma which is decided by our team of doctors after evaluating the reports.