“…In the osteoid type, the tumor arises from the subcortical or medullary portion of the bone and usually affects the long bones and vertebrae. 9 Computed tomography usually demonstrates the origin and extent of the tumor, the presence of matrix mineralization, and the tumor delineation, which is depicted as a peripheral, thin bony shell. 6 The differential diagnosis of osteoblastomas includes not only other bony neoplasms, such as osteoma, osteoid osteoma, and osteogenic sarcoma, but also fibro-osseous lesions, such as ossifying fibroma, fibrous dysplasia, and the cementing-ossifying fibroma, or cementoma.…”