Rivierez M, Vally P, Jouannelle A
Service de Neurochirurgie, CHU L a Cavale Blanche, 29609 Brest Cedex, France.
Neurochirurgie. 2001 May;47(2-3 Pt 1):137-9.
A 34-year-old man presented with recent severe headache. Neurological examination found gait disturbance and a static cerebellar syndrome. The CT scan showed a tumor located in the fourth ventricle and which presented with a density close to that of the cerebellar parenchyma, without contrast enhancement, associated with an enlargement of the third and the lateral ventricles. MRI showed that the tumor had an heterogeneous hyposignal on T1-weighted images and an hypersignal on T2-weighted images, without associated edema; the roof of the fourth ventricle was displaced upward and the brain stem forward. At operation, an encapsulated epidermal cyst, developed from the cerebellar vermis, without attachment to the floor of the fourth ventricle, was totally removed. Epidermal cysts of the fourth ventricle are unusual lesions; their capsule often adhere to the floor and cannot be totally removed. Those developed from the cerebellar vermis seem to be rarer. With the use of MRI, their true origin could be suspected. In these cases, the cysts can be totally removed, reducing the risk of recurrence
一名34岁男性因近期严重头痛就诊。神经系统检查发现步态障碍和静止性小脑综合征。CT扫描显示肿瘤位于第四脑室,密度与小脑实质相近,无强化,伴有第三脑室和侧脑室扩大。MRI显示肿瘤在T1加权图像上呈不均匀低信号,在T2加权图像上呈高信号,无相关水肿;第四脑室顶部向上移位,脑干向前移位。手术中,一个由小脑蚓部形成的包膜性表皮样囊肿,未附着于第四脑室底部,被完全切除。第四脑室表皮样囊肿是不常见的病变;其包膜常附着于底部,无法完全切除。由小脑蚓部形成的囊肿似乎更为罕见。通过MRI检查,可怀疑其真正起源。在这些病例中,囊肿可被完全切除,降低复发风险