Benign Bone Tumors and Cysts
(See also Overview of Bone and Joint Tumors.)
Simple unicameral bone cysts occur in the long bones starting distal to the epiphyseal plate in children. The cyst causes the cortex to thin and predisposes the area to a buckle-like pathologic fracture, which is usually how the cyst is recognized. Plain x-rays are usually diagnostic. Simple unicameral bone cysts typically appear as well-marginated lesions without reactive sclerosis or an expansile cortex. Smaller cysts sometimes heal without treatment. A nondisplaced fracture through small cysts may be a stimulus for healing. Larger cysts, particularly in children, may require curettage and bone grafting; however, many respond to injections of corticosteroids, demineralized bone matrix, or synthetic bone substitutes. The response may be variable and may require multiple injections. Regardless of treatment, cysts persist in about 10 to 15% of patients.
An aneurysmal bone cyst is an idiopathic expansile lesion that usually develops before age 25 yr. This cystic lesion usually occurs in the metaphyseal region of the long bones, but almost any bone may be affected. It tends to grow slowly. A periosteal new bone shell forms around the expansile lesion and is often wider than the original bone. Pain and swelling are common. The lesion may be present for a few weeks to a year before diagnosis.
The appearance on x-ray is often characteristic: The rarefied area is usually well circumscribed and eccentric; the periosteum bulges (balloons), extending into the soft tissues, and may be surrounded by new bone formation. MRI typically shows fluid-fluid levels. On imaging, some aneurysmal bone cyst–like lesions may appear more ominous, having characteristics similar to osteosarcoma, and thus should raise suspicion of telangiectatic osteosarcoma.
Surgical removal of the entire lesion is the most successful treatment; regression after incomplete removal sometimes occurs. Radiation should be avoided when possible because sarcomas occasionally develop. However, radiation may be the treatment of choice in completely surgically inaccessible vertebral lesions that are compressing the spinal cord.
Fibrous dysplasia involves abnormal bone development during childhood. It may affect one or several bones. Multiple fibrous dysplasias, cutaneous pigmentation, and endocrine abnormalities may be present (Albright syndrome or McCune-Albright syndrome). The abnormal bone lesions of fibrous dysplasia commonly stop developing at puberty. They rarely undergo malignant degeneration.
On x-ray, the lesions can appear cystic and may be extensive and deforming. On imaging, the lesions have a classic ground-glass appearance.
Bisphosphonates may help relieve pain. Progressive deformities, fractures that do not heal with immobilization, or intractable pain may be effectively treated surgically.
Osteochondromas (osteocartilaginous exostoses), the most common benign bone tumors, may arise from any bone but tend to occur near the ends of long bones. These tumors manifest most often in people aged 10 to 20 and may be single or multiple. Multiple osteochondromas tend to run in families. Secondary malignant chondrosarcoma develops in well under 1% of patients with single osteochondromas, but in about 10% of patients with multiple osteochondromas. Patients with multiple hereditary osteochondromas have more tumors and are more likely to develop a chondrosarcoma than patients with a single osteochondroma. Osteochondromas rarely cause the bone to fracture.
On imaging studies, the lesion appears as a bony prominence with a cartilage cap (usually < 2 cm) off the surface of the bone with no underlying cortex under the prominence. The medullary canal is in continuity with the base of the exostosis. The medullary canal and exostosis are confluent, and there is no true underlying cortex at the base of the exostosis. Occasionally, a painful bursa may form over the cartilage cap.
Excision is needed if the tumor is compressing a large nerve; causes pain (especially when impinging on muscle and creating an inflammatory bursa); disturbs growth; or on imaging study has a destructive appearance, soft-tissue mass, or thickened cartilaginous cap (> 2 cm) suggesting transformation into malignant chondrosarcoma. An enlarging tumor in an adult should raise concern of chondrosarcoma and the possible need for excision or biopsy.
Enchondromas may occur at any age but tend to manifest in people aged 10 to 40. They are usually located within the medullary bone metaphyseal-diaphyseal region. These tumors are usually asymptomatic but may enlarge and become painful. They are often found when x-rays are taken for another reason. Periosteal chondromas are similar cartilage lesions that occur on the surface of bones.
On x-ray, the tumor may appear as a lobulated calcified area within bone; some lesions are less calcified, with areas of stippled calcification on either plain films or CT. If adjacent to the cortex, enchondromas show minor endosteal scalloping. Almost all enchondromas have increased uptake on a bone scan and thus create false concern of cancer. X-ray findings, including MRI and CT, may be diagnostic; if they are not, and especially if the tumor (not the associated joint) is painful, the diagnosis of enchondroma should be confirmed by biopsy. To help differentiate bone pain from joint pain, the joint can be injected, usually with a long-lasting anesthetic (eg, bupivacaine); if pain persists, it may be caused by the bone lesion.
An asymptomatic enchondroma does not need biopsy, excision, or other treatment (usually curettage); however, follow-up imaging studies are indicated to rule out the rare disease progression to chondrosarcoma. These studies are done at 6 mo and again at 1 yr or whenever symptoms develop.
Patients with multiple enchondromas (Ollier disease) and especially multiple enchondromatosis with soft-tissue hemangiomas (Maffucci syndrome) have a much higher risk of chondrosarcoma.
Chondroblastoma is rare and occurs most commonly among people aged 10 to 20. Arising in the epiphysis, this tumor may continue to grow and destroy bone and the joint.
It appears on imaging studies as a sclerotic marginated cyst containing spots of punctate calcification. MRI can help diagnostically by showing significant edema around the lesion.
The tumor must be surgically removed by curettage, and the cavity must be bone grafted. Local recurrence rate is about 10 to 20%, and recurrent lesions often resolve with repeat bone curettage and bone grafting.
Chondromyxofibroma is very rare and usually occurs before age 30.
The appearance on imaging studies, which is usually eccentric, sharply circumscribed, lytic, and located near the end of long bones, suggests the diagnosis of chondromyxofibroma.
Treatment of chondromyxofibroma after biopsy is surgical excision or curettage.
Osteoid osteoma, which tends to affect young people (commonly aged 10 to 35), can occur in any bone but is most common in long bones. It can cause pain (usually worse at night, reflecting increased nocturnal prostaglandin-mediated inflammation). Pain is typically relieved by mild analgesics (particularly aspirin or other NSAIDs) that target prostaglandins. In growing children, the inflammatory response and associated hyperemia, if close to the open growth plate, may cause overgrowth and limb length discrepancy. Physical examination may reveal atrophy of regional muscles because the pain causes muscle disuse.
Characteristic appearance on imaging studies is a small radiolucent zone surrounded by a larger sclerotic zone. If a tumor is suspected, a technetium-99m bone scan should be done; an osteoid osteoma appears as an area of increased uptake. CT with fine image sequences is also done and is most helpful in distinguishing the lesion.
Ablation of the small radiolucent zone with percutaneous radiofrequency energy provides permanent relief in most cases. Most osteoid osteomas are treated by an interventional musculoskeletal radiologist using percutaneous techniques and anesthesia. Less often, osteoid osteomas are surgically curetted or excised. Surgical removal may be preferred when the osteoid osteoma is near a nerve or close to the skin (eg, spine, hands, feet) because the heat produced by radiofrequency ablation may cause damage.
Osteoblastoma is a rare benign tumor that consists of tissue histologically similar to that of an osteoid osteoma. Some experts simply consider them large osteoid osteomas (> 2 cm). Osteoblastoma is much more common among males and appears typically between ages 10 and 35. The tumor develops in the bone of the spine, legs, hands, and feet. It is a slow-growing tumor that destroys normal bone. This tumor is painful.
Imaging is with plain films, CT, and MRI. A biopsy is warranted to make an accurate diagnosis of osteoblastoma.
Treatment of osteoblastoma requires surgery, often curettage and bone grafting. The local recurrence rate for lesions that are treated with intralesional curettage may be as high as 10 to 20%. More aggressive-appearing lesions are treated with surgical en bloc resection and bony reconstruction. A variation called aggressive osteoblastoma is similar to osteosarcoma both radiographically and histologically.
Nonossifying fibroma is a benign fibrous lesion of bone that appears as a well-defined lucent cortical defect on x-ray. A very small nonossifying fibroma is called a fibrous cortical defect. These lesions are developmental defects in which parts of bone that normally ossify are instead filled with fibrous tissue. They commonly affect the metaphyses, and the most commonly affected sites are, in order, the distal femur, distal tibia, and proximal tibia. They can progressively enlarge and become multiloculated. Nonossifying fibromas are common among children. Most lesions eventually ossify and undergo remodeling, often resulting in dense, sclerotic areas. However, some lesions enlarge.
Small nonossifying fibromas are asymptomatic. However, lesions that involve nearly 50% of the bone diameter tend to cause pain and increase the risk of pathologic fracture.
Nonossifying fibromas are generally first noted incidentally on imaging studies (eg, after trauma). They typically are radiolucent, single, < 2 cm in diameter, and have an oblong lucent appearance with a well-defined sclerotic border in the cortex. They can also be mutiloculated.
Small nonossifying fibromas require no treatment and limited follow-up. Lesions that cause pain or are close to 50% of the bone diameter may warrant curettage and bone grafting to decrease risk of a pathologic fracture through the lesion.
Benign giant cell tumors of bone, which most commonly affect people in their 20s and 30s, occur in the epiphyses. These tumors are considered locally aggressive. They tend to continue to enlarge, destroy bone, and may eventually erode the rest of the bone and extend into the soft tissues. They may cause pain. These tumors are notorious for their tendency to recur. Rarely, a giant cell tumor of bone may metastasize to the lung, even though it remains histologically benign.
Benign giant cell tumors of bone appear as expansile lytic lesions on imaging. On imaging studies, there is a margin without a sclerotic rim where the tumor ends and normal trabecular bone begins. Because a giant cell tumor of bone may metastasize to the lung, a chest CT is done as part of initial staging.
Most benign giant cell tumors of bone are treated by curettage and packing with methyl methacrylate or by bone graft. To reduce recurrence rate, surgeons often prefer using an adjuvant such as thermal heat (provided by the hardening of methyl methacrylate) or treating the tumors chemically with phenol or freezing with liquid nitrogen. If a tumor is very large and destructive to the joint, complete excision with joint reconstruction may be necessary. The monoclonal antibody denosumab, a receptor activator of nuclear factor kappa-B ligand (RANKL) inhibitor, can be used in the treatment of benign giant cell tumor of bone for large, potentially nonoperable tumors (see photo Giant Cell Tumor [CT Scan]).