Bone cancer jaw symptom

Definition

A sarcoma is a bone tumor that contains cancer (malignant) cells. A benign bone tumor is an abnormal growth of noncancerous cells.

Description

A primary bone tumor originates in or near a bone. Most primary bone tumors are benign, and the cells that compose them do not spread (metastasize) to nearby tissue or to other parts of the body.

Malignant primary bone tumors account for fewer than one percent of all cancers diagnosed in the United States. They can infiltrate nearby tissues, enter the bloodstream, and metastasize to bones, tissues, and organs far from the original malignancy. Malignant primary bone tumors are characterized as either:

• Bone cancers which originate in the hard material of the bone.
• Soft-tissue sarcomas which begin in blood vessels, nerves, or tissues containing muscles, fat, or fiber.

Types of bone tumors

Osteogenic sarcoma, or osteosarcoma, is the most common form of bone cancer, accounts for six percent of all instances of the disease, and for about five percent of all cancers that occur in children. Nine hundred new cases of osteosarcoma are diagnosed in the United States every year. The disease usually affects teenagers, and is almost twice as common in boys as in girls.

Osteosarcomas, which grow very rapidly, can develop in any bone but most often occur along the edge or on the end of one of the fast-growing long bones that support the arms and legs. About 80% of all osteosarcomas develop in the parts of the upper and lower leg nearest the knee (the distal femur or in the proximal tibia). The next likely location for an osteosarcoma is the bone of the upper arm closest to the shoulder (the proximal humerus).

Ewing's sarcoma is the second most common form of childhood bone cancer. Accounting for fewer than five percent of bone tumors in children, Ewing's sarcoma usually begins in the soft tissue (the marrow) inside bones of the leg, hips, ribs, and arms. It rapidly infiltrates the lungs, and may metastasize to bones in other parts of the body.

More than 80% of patients who have Ewing's sarcoma are white, and the disease most frequently affects children between ages 5-9, and young adults between ages 20-30. About 27% of all cases of Ewing's sarcoma occur in children under age 10, and 64% occur in adolescents between ages 10-20.

Chondrosarcomas are cancerous bone tumors that most often appear in middle age. Usually originating in strong connective tissue (cartilage) in ribs or leg or hip bones, chondrosarcomas grow slowly. They rarely spread to the lungs. It takes years for a chondrosarcoma to metastasize to other parts of the body, and some of these tumors never spread.

Parosteal osteogenic sarcomas, fibrosarcomas, and chordomas are rare. Parosteal osteosarcomas generally involve both the bone and the membrane that covers it. Fibrosarcomas originate in the ends of the bones in the arm or leg, and then spread to soft tissue. Chordomas develop on the skull or spinal cord.

Osteochondromas, which usually develop between age 10-20, are the most common noncancerous primary bone tumors. Giant cell tumors generally develop in a section of the thigh bone near the knee. Giant cell tumors are originally benign but sometimes become malignant.

Causes & symptoms

The cause of bone cancer is unknown, but the tendency to develop it may be inherited. Children who have bone tumors are often tall for their age, and the disease seems to be associated with growth spurts that occur during childhood and adolescence. Injuries can make the presence of tumors more apparent but do not cause them.

A bone that has been broken or exposed to high doses of radiation used to treat other cancers is more likely than other bones to develop osteosarcoma. A history of noncancerous bone disease also increases bone-cancer risk.

The amount of radiation in diagnostic x rays poses little or no danger of bone-cancer development, but children who have a family history of the most common childhood cancer of the eye (retinoblastoma), or who have inherited rare cancer syndromes have a greater-than-average risk of developing bone cancer. Exposure to chemicals found in some paints and dyes can slightly raise the risk.

Both benign and malignant bone tumors can distort and weaken bone and cause pain, but benign tumors are generally painless and asymptomatic.

It is sometimes possible to feel a lump or mass, but pain in the affected area is the most common early symptom of bone cancer. Pain is not constant in the initial stages of the disease, but it is aggravated by activity and may be worst at night. If the tumor is located on a leg bone, the patient may limp. Swelling and weakness of the limb may not be noticed until weeks after the pain began.

Other symptoms of bone cancer include:

• A bone that breaks for no apparent reason
• Difficulty moving the affected part of the body
• Fatigue
• Fever
• A lump on the trunk, an arm or leg, or another bone
• Persistent, unexplained back pain
• Weight loss.

Diagnosis

Physical examination and routine x rays may yield enough evidence to diagnose benign bone tumors, but removal of tumor tissue for microscopic analysis (biopsy) is the only sure way to rule out malignancy.

A needle biopsy involves using a fine, thin needle to remove small bits of tumor, or a thick needle to extract tissue samples from the innermost part (the core) of the growth. An excisional biopsy is the surgical removal of a small, accessible tumor. An incisional biopsy is performed on tumors too large or inaccessible to be completely removed. The surgeon performing an incisional biopsy cuts into the patient's skin and removes a portion of the exposed tumor. Performed under local or general anesthetic, biopsy reveals whether a tumor is benign or malignant and identifies the type of cancer cells the malignant tumor contains.

Bone cancer is usually diagnosed about three months after symptoms first appear, and 20% of malignant tumors have metastasized to the lungs or other parts of the body by that time.