Mashiyama S, Sakurai Y, Kayama T, Nishino A, Jokura H
Department of Neurosurgery, National Sendai Hospital.
No Shinkei Geka. 1994 Feb;22(2):165-8.
A 28-year-old woman was admitted to our clinic due to psychomotor epilepsy. Craniogram, CT scan demonstrated a calcified lesion in the frontal, parasagittal region. MR proton images showed a mixed hyper-and hypodense lesion. The tumor originated from the frontal bone and was totally removed using airdrill safely. Histological findings revealed osteochondroma originating in the frontal bone is rare, and diagnostic procedures and surgical management of this tumor are discussed.
一名28岁女性因精神运动性癫痫入住我院。颅骨X线片、CT扫描显示额部矢状旁区域有一钙化病灶。磁共振质子图像显示为混合性高低密度病灶。肿瘤起源于额骨，使用气钻安全地将其完全切除。组织学检查结果显示，起源于额骨的骨软骨瘤很罕见，并对该肿瘤的诊断方法和手术治疗进行了讨论。
