McLeod R A, Dahlin D C, Beabout J W
AJR Am J Roentgenol. 1976 Feb;126(2):321-5. doi: 10.2214/ajr.126.2.321.
Benign osteoblastoma is a rare tumor, more frequent in males, usually occurring in patients under the age of 30 years, and is seen most frequently in the spine, femur, tibia, and mandible. Its varied roentgenographic appearance may suggest a large osteoid osteoma or an aneurysmal bone cyst, but about one-fourth of cases present a picture consistent with a malignant neoplasm. The roentgen changes in the spine are frequently subtle and require care for identification. Differentiation from osteogenic sarcoma is sometimes difficult even with histological material, because some low grade osteogenic sarcomas contain areas resembling osteoblastoma. Conservative surgery is the treatment of choice for osteoblastoma.
骨母细胞瘤是一种罕见肿瘤,男性更为常见,通常发生于30岁以下患者,最常见于脊柱、股骨、胫骨和下颌骨。其多样的X线表现可能提示为大型骨样骨瘤或动脉瘤样骨囊肿,但约四分之一的病例呈现出与恶性肿瘤相符的影像。脊柱的X线改变常常不明显,需要仔细辨认。即使有组织学材料,有时也难以与骨肉瘤鉴别,因为一些低级别骨肉瘤含有类似骨母细胞瘤的区域。保守手术是骨母细胞瘤的首选治疗方法。