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Related to osteoma cutis: Calcinosis cutis, Albright hereditary osteodystrophy
a tumor, benign or malignant, composed of bony tissue; a hard tumor of bonelike structure developing on a bone (homoplastic osteoma) or other structures (heteroplastic osteoma).
Symptoms. Symptoms of bone cancer are pain, swelling, and disability in the area of the diseased bone. The pain at first is mild, stops and starts again, and then becomes increasingly severe. Swelling may appear soon after the first signs of pain, but often it cannot be seen until later. The disability may affect a nearby joint, such as the knee, shoulder, or hip. There may also be a hard, painful lump over which the skin moves freely. The skin temperature in the area may be slightly elevated.
Diagnosis and Treatment. Diagnosis of bone tumor is made after examination of x-ray film and a microscopic study of the suspected tissue. Malignant tumors can be treated by radiotherapy and surgery during the early stage of development. The prognosis for these tumors is grave, however. Hormone therapy and medication can also be helpful in certain types of the disease.
osteoma cu´tis progressive dermal ossification during childhood, with development of hard, round to irregular nodules representing islands of heterotopic bone within the dermis or subcutis, followed by coalescence of the lesions into plaques, and later by invasion of ossification into deep connective tissues. It may be sporadic or inherited as an autosomal dominant trait. Called also progressive osseous heteroplasia.
osteoma du´rum (osteoma ebur´neum) one containing hard bony tissue.
osteoma medulla´re one containing marrow spaces.
osteoid osteoma see osteoid osteoma.
osteoma spongio´sum (spongy osteoma) one containing cancellated bone.
cutaneous ossification usually secondary to calcification in foci of degeneration in tumors or inflammatory lesions or, rarely, primary new bone formation in normal skin, often associated with Albright hereditary ostrodystrophy.