Nakatani Tetsuya, Yamamoto Tetsuji, Akisue Toshihiro, Marui Takashi, Hitora Toshiaki, Kawamoto Teruya, Nagira Keiko, Fujita Ikuo, Matsumoto Keiji, Yoshiya Shinichi, Kurosaka Masahiro
Department of Orthopaedic Surgery, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, Japan.
Skeletal Radiol. 2004 Feb;33(2):107-11. doi: 10.1007/s00256-003-0723-0. Epub 2004 Jan 9.
Osteoblastomas located on the surface of the cortical bone, so-called periosteal osteoblastomas, are extremely rare. We report on a case of periosteal osteoblastoma arising from the posterior surface of the right distal femur in a 17-year-old man. Roentgenographic, computed tomographic, magnetic resonance imaging, and histologic features of the case are presented. Periosteal osteoblastoma should be radiologically and histologically differentiated from myositis ossificans, avulsive cortical irregularity syndrome, osteoid osteoma, parosteal osteosarcoma, periosteal osteosarcoma, and high-grade surface osteosarcoma. Although periosteal osteoblastoma is rare, this tumor should be included in the differential diagnosis of surface-type bone tumors.
位于皮质骨表面的成骨细胞瘤,即所谓的骨膜成骨细胞瘤,极为罕见。我们报告一例17岁男性右股骨远端后侧发生的骨膜成骨细胞瘤病例。文中展示了该病例的X线、计算机断层扫描、磁共振成像及组织学特征。骨膜成骨细胞瘤在放射学和组织学上应与骨化性肌炎、撕脱性皮质不规则综合征、骨样骨瘤、骨旁骨肉瘤、骨膜骨肉瘤及高级别表面骨肉瘤相鉴别。尽管骨膜成骨细胞瘤罕见,但在表面型骨肿瘤的鉴别诊断中应考虑到这种肿瘤。