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Giant Cell Tumor of Bone
A giant cell tumor of bone is a type of benign (noncancerous) tumor that grows at the ends of the body's long
bones. Most often, the tumors develop at the lower end of the femur (thighbone) or upper end of the tibia
(shinbone), close to the knee joint.

Giant cell tumors typically occur in young adults, and are slightly more common in females. They are quite rare,
occurring in only about one out of every one million people per year.

Although giant cell tumors are not cancerous, they are aggressive and can destroy the surrounding bone.
Treatment for a giant cell tumor almost always involves surgery to remove the tumor and prevent damage to the
bone near the affected joint.

Giant cell tumors are named for the characteristic way they look when viewed under the microscope. When
viewed microscopically, the tumors consist of many unusually large or "giant" cells. These cells are formed by the
fusion of several individual cells into a single, larger cell.

Many types of bone tumors and other conditions (including normal bone) contain giant cells. The diagnosis of
giant cell tumor of bone is made when a large number of giant cells are seen among a background of other
abnormal cells.

While most bone tumors occur in the flared area near the ends of the body's long bones (metaphysis), giant cell
tumors occur almost exclusively in the end portion of the long bones (epiphysis), directly next to the joints.

Most often, the tumors occur close to the knee joint—either in the lower end of the thighbone (femur) or the upper
end of the shinbone (tibia).

Illustration shows a giant cell tumor at the lower end of the thighbone. This is a common location for the tumors to occur.

Formed by the fusion of several cells, giant cells show multiple nuclei when viewed under a microscope.
Reproduced from Raskin KA, Schwab JH, Mankin HJ, Springfield DS, Hornicek FJ: Giant cell tumor of bone. J Am Acad Orthop Surg
2013; 21: 118-126

Other common locations include the:

 Wrist (lower end of the lower arm bone)

 Hip (upper end of the thighbone)
 Shoulder (upper end of the upper arm bone)
 Lower back (connection of the spine and pelvis)

Most giant cell tumors occur in patients between 20 and 40 years of age. Only rarely do they occur in children or
in adults older than 65 years of age. They occur slightly more often in females.

While giant cell tumors are typically benign (noncancerous), they can grow quickly and destroy bone close to a
joint. In rare cases, a giant cell tumor may spread, or metastasize, to the lungs.

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The cause of giant cell tumors is unknown. The tumors occur spontaneously. They are not known to be caused
by trauma, environmental factors, or diet. Giant cell tumors of bone are not inherited.

In rare cases, the tumors may be associated with overactivity of the parathyroid glands—a condition known as

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The most common symptom of a giant cell tumor is pain in the area of the tumor. The patient may also have pain
with movement of the nearby joint. This pain usually increases with activity and decreases with rest.

The pain is usually mild at first, but gets worse over time as the tumor increases in size. Occasionally, the bone
weakened by the tumor breaks and causes the sudden onset of severe pain.

Sometimes, the patient will have no pain at all, but will notice a mass or swollen area instead.

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Doctor Examination
Your doctor will perform a thorough physical examination and use x-rays and other tests to diagnose a giant cell

X-ray. This study provides images of dense structures, such as bone. Your doctor will order an x-ray to help
confirm the diagnosis.

On x-ray, a giant cell tumor appears as a destructive (lytic) lesion next to a joint. Occasionally, the involved area
of bone will be surrounded by a thin rim of white bone, which may be either complete or incomplete. There may
also be expansion of the involved area of bone.
X-rays from the front (left) and side (right) show a giant cell tumor in the lower end of the thighbone.
Reproduced from Lewis VO, Aboulafia AJ: Giant cell tumor of bone. Orthopaedic Knowledge Online Journal 2007; 5(5). Accessed
August 2016.

X-ray shows a giant cell tumor in the lower end of the radius bone in the wrist.
Reproduced from Johnson TR, Steinbach LS (eds.): Essentials of Musculoskeletal Imaging. Rosemont, IL. American Academy of
Orthopaedic Surgeons, 2004, p. 120.

Other imaging studies. Your doctor may order a magnetic resonance imaging (MRI) scan or computerized
tomography (CT) scan to better evaluate the tumor and the area surrounding it.

A CT scan or chest x-ray may also be done at the time of the initial diagnosis to determine if the tumor has
spread to the lungs.
MRI scan shows a giant cell tumor at the upper end of the shinbone.
Reproduced from Biermann S (ed): Orthopaedic Knowledge Update 3, Musculoskeletal Tumors. Rosemont IL. American Academy of
Orthopaedic Surgeons, 2013, pp. 133-146.

Bone scan. In some cases, your doctor may order a bone scan. During this test, a very small amount of
radioactive dye is injected into the body intravenously. Giant cell tumors generally cause an increased uptake of
the radioactive material and appear as a "hot spot" in the bone where the tumor is located.

Biopsy. A biopsy may be needed to confirm the diagnosis of a giant cell tumor. In a biopsy, a sample of tissue is
taken from the tumor and examined under a microscope.

A biopsy can be performed under local anesthesia with a needle or as a small open operation.

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Without treatment, a giant cell tumor will continue to grow and destroy the surrounding bone, so treatment is
always necessary. The goals of treatment are to:

 Remove the tumor

 Prevent damage to the bone

Surgery is the preferred treatment for giant cell tumors; however, there are some cases in which a tumor cannot
be removed safely or effectively through surgery. In this case, your doctor may recommend nonsurgical

Nonsurgical Treatment
Nonsurgical treatment may include:

Radiation. Radiation therapy may sometimes be used to shrink giant cell tumors in areas where surgery may be
difficult to perform without damaging sensitive tissues—such as the spine. However, radiation therapy can result
in the formation of cancer in some patients, so it is used only in the most difficult cases.

Tumor embolization. During this procedure, specific arteries that supply blood to the tumor are blocked off.
Without their supply of oxygen and nutrients, the tumor cells begin to die. Most often, embolization is performed
prior to surgery, but it may also be used on its own in cases where surgery cannot be performed.

Medication. The FDA has recently approved the use of an injectable medication for the treatment of giant cell
tumors. The medication works by targeting a special receptor on the tumor cells. This decreases activity and
slows down the breakdown of bone. The medication is sometimes used in cases where surgery cannot be
performed or for recurrent tumors.
Surgical Treatment
Surgery has proven to be the most effective treatment for giant cell tumors. Surgical treatment may include:

Curettage. Curettage is the surgical procedure most commonly used to treat giant cell tumors. In curettage,
special instruments are used to scrape the tumor out of the bone.

Bone graft. After curettage, the cavity is filled with a bone graft to help stabilize the bone. A bone graft is bone
taken from a donor (allograft) or from another bone in your own body (autograft)—most often the hip.

Your doctor may also use a bone cement mixture to fill the hole. Sometimes, additional chemicals, such as liquid
nitrogen, hydrogen peroxide, or phenol, are placed inside the bone cavity to try to reduce the risk of recurrence.

(Left) Preoperative x-ray shows a giant cell tumor in the lower end of the thighbone. (Right) X-ray shows the tumor after
treatment with curettage and packing with bone cement.
Reproduced from Raskin KA, Schwab JH, Mankin HJ, Springfield DS, Hornicek FJ: Giant cell tumor of bone. J Am Acad Orthop Surg
2013; 21: 118-126