Spine tumor is the abnormal growth of uncontrolled tissues or cells in and around the spinal cord. Tumors can either be cancerous (malignant) or non-cancerous (benign). Some of the commonly occurring benign spinal tumors are osteoma, osteoblastoma, hemangioma, and osteochondroma. Most commonly occurring malignant spinal tumors are chondrosarcoma, Ewing’s sarcoma, lymphoma, osteosarcoma, and multiple myeloma. Tumors that begin in the spine are called as primary spinal tumors. Tumors that spread to the spine from other parts such as the breast, prostate, lung, and other areas are called secondary spinal tumors.
The cause of primary spinal tumors is not known, but may occur with genetic defects.
Secondary spinal tumors occur when the cancer cells arise from kidneys, lungs, breasts, and spreads to the spine. Other causes include:
- Rapid division of cancer cells in the nerves, bones, or cartilage of the spine
- Exposure to radiations and chemicals
- Hereditary – Neurofibromatosis is a hereditary tumor of the spinal nerves
People with spine tumor experience persistent and chronic back pain, numbness, burning and tingling sensation, loss of sensation in legs, arms, ankle, knee, and difficulty in balancing, and also experience bladder or bowel control problems.
Spine cancer can be diagnosed by neurological examination which identifies the exact location of the tumor. Other imaging tests done to confirm the spinal tumor may include cerebrospinal fluid (CSF) examination, myelogram, and spine computed tomography scan, spine magnetic resonance imaging scan, and spine X-ray. In addition to these tests, bone scan and positron emission tomography (PET) scan are also done. After the tumor is found, biopsy is done to identify the type of tumor and provide necessary treatment.
Medications such as corticosteroids and anti-inflammatory drugs are prescribed to reduce inflammation and swelling around the spinal cord. External braces are also used which provide support and control pain.
Other treatments include chemotherapy, radiation therapy, surgery, and physical therapy which may provide permanent relief.
- Surgery: It is done to remove the tumor confined only to one portion of the spine. To minimize nerve damage, electrodes are used to test different nerves of the spine. In some cases sound waves are used to break tumors and the remaining tissues are removed.
- Radiation therapy: This method uses high beam of radiations to destroy the cancer cells. It is used after surgery to destroy the remaining cancer cells. An advanced device called cyberknife, painless and non-invasive treatment that passes high doses of radiations to the targeted areas of the spinal cord is used in radiotherapy.
- Chemotherapy: Combination of anti-cancer drugs is used to destroy the cancer cells. Chemotherapy is used to shrink the cancer cells, to stop the division of cancer cells, and prevent them from spreading to surrounding tissues. The drugs enter the bloodstream and reach the cancer cells to destroy them. Some of the commonly used drugs are methotrexate, doxorubicin, cyclophosphamide, carboplatin, and ifosfamide.
Some of the complications observed after surgery are temporary loss of sensation, nerve tissue damage, and bleeding.
Physical therapy: Exercises may be needed to improve muscle strength and the ability to function independently.