Hatori M, Okada K, Nishida J, Kokubun S
Department of Orthopaedic Surgery, Tohoku University School of Medicine, Sendai, Japan.
Arch Orthop Trauma Surg. 2001 Nov;121(10):594-7. doi: 10.1007/s004020100301.
Periosteal Ewing's sarcoma is very rare. In this report, we describe three cases of periosteal Ewing's sarcoma, illustrating the principal clinical, radiographic, and histologic features. The patients were aged 15, 16, and 20 years old, with an average of 17 years. The tumor occurred in the humerus in two and in the femur in one. Plain radiography showed a laminated periosteal reaction with a Codman's triangle over a subperiosteal soft-tissue mass or saucerization. The unusual site of Ewing's sarcoma was clearly visualized by computed tomography (CT) and magnetic resonance imaging (MRI) and confirmed by histological examination. Chemotherapy and/or irradiation was employed before and after wide excision. The patients have survived an average of 6 years after the primary surgery.
骨膜尤文肉瘤非常罕见。在本报告中,我们描述了3例骨膜尤文肉瘤病例,阐述了其主要的临床、影像学和组织学特征。患者年龄分别为15岁、16岁和20岁,平均年龄17岁。2例肿瘤发生于肱骨,1例发生于股骨。X线平片显示骨膜呈分层状反应,骨膜下软组织肿块或骨质碟形化区域可见科德曼三角。尤文肉瘤的异常部位通过计算机断层扫描(CT)和磁共振成像(MRI)清晰显示,并经组织学检查证实。在广泛切除前后采用了化疗和/或放疗。患者在初次手术后平均存活了6年。