Miyamori T, Mizukoshi H, Yamano K, Takayanagi N, Sugino M, Hayase H, Ito H
Department of Neurosurgery, Toyama Municipal Hospital.
Neurol Med Chir (Tokyo). 1990 Apr;30(4):263-7. doi: 10.2176/nmc.30.263.
The authors report the case of a 54-year-old male who was found to have a large intracranial chondrosarcoma at the site from which chondromas had been partially removed twice, 6 and 10 years previously. On the third admission, the second through tenth and the twelfth cranial nerves on the right side were involved. Computed tomographic scans showed a large mass in the right middle and posterior fossae and the right ethmoid sinus. Angiography demonstrated an extradural mass in the right middle fossa. The tumor in the middle and posterior fossae was subtotally removed, and second, third, and eighth cranial nerve function improved postoperatively. Histological examination of tumor specimens showed active proliferation of poorly differentiated cartilagenous cells, suggestive of sarcomatous transformation of the pre-existing chondroma. It is emphasized that chondromas should be removed as completely as possible and that patients must be followed carefully after surgery.
作者报告了一例54岁男性病例,该患者在6年前和10年前曾两次部分切除软骨瘤的部位被发现患有大型颅内软骨肉瘤。第三次入院时,右侧第二至第十和第十二对颅神经受累。计算机断层扫描显示右侧中颅窝、后颅窝及右侧筛窦有一个大肿块。血管造影显示右侧中颅窝有一个硬膜外肿块。中颅窝和后颅窝的肿瘤被次全切除,术后第二、第三和第八对颅神经功能有所改善。肿瘤标本的组织学检查显示低分化软骨细胞活跃增殖,提示先前存在的软骨瘤发生了肉瘤样转化。强调软骨瘤应尽可能完全切除,术后必须对患者进行仔细随访。