Paviour Dominic C, Jäger H Rolf, Wilkinson Leonora, Jahanshahi Marjan, Lees Andrew J
The Sara Koe PSP Research Centre, The Institute of Neurology, UCL, London, United Kingdom.
Mov Disord. 2006 Dec;21(12):2260-2. doi: 10.1002/mds.20981.
Holmes tremor has a characteristic rest, intention, and postural component. The syndrome arises as a consequence of a lesion in the upper brainstem and cerebral peduncles, which, it is postulated, interrupts the cerebello-rubrothalamic pathway. Ataxia, ophthalmoplegia, and bradykinesia are associated features. We present a case of Holmes tremor secondary to a midbrain cavernoma. Modern neuroimaging techniques in this case confirm that a combination of damage to the cerebello-rubrothalamic pathway and the nigrostriatal pathway is required for the full Holmes tremor syndrome to occur.
霍姆斯震颤具有特征性的静止性、意向性和姿势性震颤成分。该综合征是由上脑干和大脑脚的病变引起的,据推测,这种病变会中断小脑-红核-丘脑通路。共济失调、眼肌麻痹和运动迟缓是相关的特征。我们报告一例继发于中脑海绵状血管瘤的霍姆斯震颤病例。该病例中的现代神经影像学技术证实,小脑-红核-丘脑通路和黑质纹状体通路的联合损伤是霍姆斯震颤综合征完全发生所必需的。