Wada Y, Kita Y, Yamamoto T
Department of Neurology, Osaka Saiseikai Nakatsu Hospital.
Rinsho Shinkeigaku. 2000 Jun;40(6):582-5.
A 78-year-old right-handed man with idiopathic orthostatic hypotension and a history of Hashimoto's thyroiditis presented over 2 years with recurrent, stereotyped attacks of bilateral limb shaking and metamorphopsia, which were precipitated by standing more than 3 or 4 minutes, or walking a few meters. These symptoms would resolve upon squatting or lying down and did not occur spontaneously at rest. He did not lose consciousness during the attacks. Speech, power, and sensation were preserved during these attacks. He had no history of seizures or habit of smoking. On examination, his supine blood pressure was 110/60 mmHg, and 62/27 mmHg on standing, with the pulse rate being 61/min and 66/min, respectively. Although he showed orthostatic hypotension, he did not complain of fainting or lightheadedness on standing alone. Magnetic resonance imaging of the brain revealed mild periventricular white matter changes and multiple small ischemic lesions bilaterally in the cerebral deep white matter. An electroencephalogram (EEG) showed mild, generalized slowing of nonspecific feature. EEG monitoring during a limb shaking episode showed no epileptiform abnormalities. Cerebral angiogram revealed a moderate degree of stenosis of the left internal carotid and a mild degree of stenosis of the right internal carotid, the right vertebral arteries and the left vertebral arteries. A single-photon emission computed tomography (SPECT) showed a moderate compromise of perfusion of the left internal carotid territory. After managing both hypotension and orthostatic hypotension with antihypotensive medication and levothyroxine sodium, his symptoms dramatically disappeared. Thus, we diagnosed that transient hemodynamic insufficiency due to combination of vascular stenosis and hypotension was the cause of these symptoms. Limb shaking is a well-described presentation of carotid artery occlusive disease and is usually unilateral. Bilateral limb shaking is rare and only 2 cases have been reported. Metamorphopsia is also a rare symptom of vertebrobasilar ischemia. We suggest that bilateral limb shaking correlates with hypoperfusion in the anterior border zones and metamorphopsia with that in the posterior border zones of both hemispheres. Hemodynamic TIA should be considered as a cause of movement disorders affecting four limbs.
一名78岁右利手男性,患有特发性直立性低血压及桥本甲状腺炎病史,2年来反复出现双侧肢体抖动和视物变形的刻板发作,站立超过3或4分钟或行走数米可诱发这些症状。这些症状在蹲下或躺下时会缓解,休息时不会自发出现。发作期间他未失去意识。发作期间言语、肌力和感觉均保留。他无癫痫病史及吸烟习惯。检查时,他仰卧位血压为110/60 mmHg,站立时为62/27 mmHg,脉率分别为61次/分和66次/分。虽然他有直立性低血压,但单独站立时并未诉晕厥或头晕。脑部磁共振成像显示轻度脑室周围白质改变及双侧脑深部白质多发小缺血性病灶。脑电图(EEG)显示轻度、广泛性非特异性减慢。肢体抖动发作期间的EEG监测未显示癫痫样异常。脑血管造影显示左颈内动脉中度狭窄,右颈内动脉、右椎动脉及左椎动脉轻度狭窄。单光子发射计算机断层扫描(SPECT)显示左颈内动脉供血区灌注中度受损。在用抗低血压药物和左甲状腺素钠治疗低血压和直立性低血压后,他的症状显著消失。因此,我们诊断血管狭窄和低血压共同导致的短暂血流动力学不足是这些症状的原因。肢体抖动是颈动脉闭塞性疾病的一种常见表现,通常为单侧。双侧肢体抖动罕见,仅报道过2例。视物变形也是椎基底动脉缺血的罕见症状。我们认为双侧肢体抖动与双侧大脑前交界区灌注不足相关,视物变形与双侧大脑后交界区灌注不足相关。血流动力学短暂性脑缺血发作应被视为影响四肢运动障碍的一个原因。