Wei Tz-Shiang, Hsu Chun-Sheng, Lee Yu-Chun, Chang Shin-Tsu
aDepartment of Physical Medicine and Rehabilitation bDepartment of Pediatrics and Child Health Care, Taichung Veterans General Hospital, Taichung cDepartment of Physical Medicine and Rehabilitation, School of Medicine, National Defense Medical Center, Taipei, Taiwan.
Medicine (Baltimore). 2017 Nov;96(46):e8633. doi: 10.1097/MD.0000000000008633.
Holmes' tremor is an uncommon neurologic disorder following brain insults, and its pathogenesis is undefined. The interruption of the dento-rubro-thalamic tract and secondary deterioration of the nigrostriatal pathway are both required to initiate Holmes' tremor. We used nuclear medicine imaging tools to analyze a patient with concurrent infarction in different zones of each side of the thalamus. Finding whether the paramedian nuclear groups of the thalamus were injured was a decisive element for developing Holmes' tremor.
A 36-year-old woman was admitted to our department due to a bilateral paramedian thalamic infarction. Seven months after the stroke, a unilaterally involuntary trembling with irregularly wavering motions occurring in both her left hand and forearm.
Based on the distinct features of the unilateral coarse tremor and the locations of the lesions on the magnetic resonance imaging (MRI), the patient was diagnosed with bilateral paramedian thalamic infarction complicated with a unilateral Holmes' tremor.
The patient refused our recommendation of pharmacological treatment with levodopa and other dopamine agonists based on personal reasons and was only willing to accept physical and occupational training programs at our outpatient clinic.
We utilized serial anatomic and functional neuroimaging of the brain to survey the neurologic deficit. A brain magnetic resonance imaging showed unequal recovery on each side of the thalamus. The residual lesion appeared larger in the right-side thalamus and had gathered in the paramedian area. A brain perfusion single-photon emission computed tomography (SPECT) revealed that the post-stroke hypometabolic changes were not only in the right-side thalamus but also in the right basal ganglion, which was anatomically intact. Furthermore, the brain Technetium-99m-labeled tropanes as a dopamine transporter imaging agents scan ( Tc-TRODAT-1) displayed a secondary reduction of dopamine transporters in the right nigrostriatal pathway which had resulted from the damage on the paramedian nuclear groups of the right-side thalamus.
Based on the functional images, we illustrated that a retrograde degeneration originating from the thalamic paramedian nuclear groups, and extending forward along the direct innervating fibers of the mesothalamic pathway, played an essential role towards initiating Holmes' tremor.
霍姆斯震颤是一种脑损伤后罕见的神经系统疾病,其发病机制尚不清楚。齿状红核丘脑束中断和黑质纹状体通路继发性退变都是引发霍姆斯震颤所必需的。我们使用核医学成像工具分析了一名双侧丘脑不同区域同时发生梗死的患者。丘脑旁正中核团是否受损是发生霍姆斯震颤的决定性因素。
一名36岁女性因双侧丘脑旁正中梗死入住我科。中风七个月后,她的左手和前臂出现单侧不自主颤抖,动作不规则且摇摆不定。
根据单侧粗大震颤的明显特征以及磁共振成像(MRI)上病变的位置,该患者被诊断为双侧丘脑旁正中梗死并发单侧霍姆斯震颤。
患者基于个人原因拒绝了我们用左旋多巴和其他多巴胺激动剂进行药物治疗的建议,只愿意在我们的门诊接受物理和职业训练项目。
我们利用大脑的系列解剖和功能神经成像来检查神经功能缺损情况。脑部磁共振成像显示丘脑两侧恢复情况不同。右侧丘脑残留病变看起来更大,且集中在旁正中区域。脑灌注单光子发射计算机断层扫描(SPECT)显示,中风后的低代谢变化不仅出现在右侧丘脑,还出现在解剖结构完整的右侧基底神经节。此外,作为多巴胺转运体成像剂的脑99m锝标记托烷扫描(Tc-TRODAT-1)显示,右侧黑质纹状体通路中多巴胺转运体继发性减少,这是由右侧丘脑旁正中核团受损所致。
基于功能图像,我们阐明了起源于丘脑旁正中核团、沿中脑丘脑通路的直接支配纤维向前延伸的逆行性退变,在引发霍姆斯震颤中起重要作用。