Nakai H, Kubota T, Yamamoto K, Yoshida H, Koyama S, Hodozuka A, Tanaka T
Department of Neurosurgery, Asahikawa Medical College, Midorigaoka Higashi 2-1-1-1, Asahikawa, Hokkaido 078-8510, Japan.
No Shinkei Geka. 2001 May;29(5):439-44.
We present a case of tumoral multiple sclerosis in a 66-year-old male and emphasize two clinical features: (1) Multiple well-demarcated massive enhanced lesions except for the central area, which was accompanied with severe perifocal edema, occurred within the cerebral hemispheres and should be strongly considered in the diagnosis of mass lesions. The patient underwent partial removal of the mass lesion. The initial histopathological diagnosis of the surgical specimen was astrocytoma grade II. (2) Multiple lesions disappeared completely for one and half months after starting medication using steroid. The reexamination of the surgical specimen was compatible with that of multiple sclerosis. Again, half a month after remission, multiple enhanced lesions without perifocal edema developed in the cerebral and cerebellar hemisphere. The difficulty of the initial diagnosis of multiple sclerosis with severe perifocal edema was discussed, based on our experience.
我们报告一例66岁男性的肿瘤样多发性硬化症病例,并强调两个临床特征:(1)脑半球内出现多个边界清晰的大片强化病灶,中央区域除外,伴有严重的病灶周围水肿,在诊断占位性病变时应高度考虑。患者接受了部分肿瘤切除术。手术标本的初始组织病理学诊断为II级星形细胞瘤。(2)开始使用类固醇药物治疗一个半月后,多个病灶完全消失。手术标本的复查结果与多发性硬化症相符。再次,缓解半个月后,大脑和小脑半球出现多个无病灶周围水肿的强化病灶。基于我们的经验,讨论了伴有严重病灶周围水肿的多发性硬化症初始诊断的困难。