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Positional down beating nystagmus in 50 patients: cerebellar disorders and possible anterior semicircular canalithiasis

机译:位置向下跳动性眼球震颤50例:小脑疾病和可能的前半规

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摘要

Objectives: To clarify the clinical significance of positional down beat nystagmus (pDBN). Methods: A discussion of the neuro-otological findings in 50 consecutive patients with pDBN. Results: In 38 patients there was evidence of CNS disease (central group) but in 12 there was not (idiopathic group). In the CNS group, presenting symptoms were gait, speech, and autonomic dysfunction whereas in the idiopathic group patients mostly reported positional vertigo. The main neurological and oculomotor signs in the CNS group were explained by cerebellar dysfunction, including 13 patients with multiple system atrophy. In patients with multiple system atrophy with a prominent extrapyramidal component, the presence of pDBN was helpful in the differential diagnosis of atypical parkinsonism. No patient with pDBN had the Arnold-Chiari malformation, a common cause of constant down beat nystagmus (DBN). In the idiopathic group, the pDBN had characteristics which suggested a peripheral labyrinthine disorder: vertigo, adaptation, and habituation. In six patients an additional torsional component was found (concurrently with the pDBN in three). Features unusual for peripheral disorder were: bilateral positive Dix-Hallpike manoeuvre in nine of 12 patients and selective provocation by the straight head-hanging manoeuvre in two Conclusion: It is argued that some patients with idiopathic pDBN have benign paroxysmal positional vertigo (BPPV) with lithiasis of the anterior canal. The torsional component may be weak, because of the predominantly sagittal orientation of the anterior canal, and may not be readily seen clinically. Nystagmus provocation by bilateral Dix-Hallpike and straight head-hanging may be explained by the vertical upwards orientation of the ampullary segment of the anterior canal in the normal upright head position. Such orientation makes right-left specificity with the Dix-Hallpike manoeuvre less important than for posterior canal BPPV. This orientation requires a further downwards movement of the head, often achieved with the straight head-hanging position, to provoke migration of the canaliths. The straight head-hanging manoeuvre should be carried out in all patients with a history of positional vertigo and a negative Dix-Hallpike manoeuvre.
机译:目的:阐明位置下降拍打性眼球震颤(pDBN)的临床意义。方法:讨论连续50例pDBN患者的神经耳病学发现。结果:38例有CNS疾病的证据(中枢组),但12例没有(中枢神经系统疾病)。在中枢神经系统组中,表现出的症状是步态,言语和自主神经功能障碍,而在特发性组中,患者大多报告了位置性眩晕。中枢神经系统组的主要神经系统和动眼症状由小脑功能障碍解释,其中包括13例多系统萎缩患者。在具有突出的锥体外系成分的多系统萎缩患者中,pDBN的存在有助于非典型帕金森病的鉴别诊断。 pDBN的患者均未出现Arnold-Chiari畸形,这是持续性下跳式眼球震颤(DBN)的常见原因。在特发性组中,pDBN具有提示周围性迷宫疾病的特征:眩晕,适应性和习惯性。在6例患者中发现了额外的扭转成分(同时有3例同时存在pDBN)。周围疾病异常的特征是:12例患者中有9例双侧Dix-Hallpike阳性,而2例患者采用直接头顶悬挂术进行选择性挑衅结论:有人认为某些特发性pDBN患者存在良性阵发性位置性眩晕(BPPV)前管结石。由于主要是前管的矢状位,因此扭转分量可能较弱,临床上可能不容易看到。双侧Dix-Hallpike引起的眼球震颤和笔直的悬挂可通过正常直立头部位置的前管壶腹节垂直向上定向来解释。这种定向使得Dix-Hallpike动作的左右特异性不如后管BPPV重要。这种定向要求头部进一步向下运动,通常是通过将头部垂直的姿势来实现的,以促使小管移动。具有位置性眩晕病史且Dix-Hallpike动作为阴性的所有患者均应进行直接的头顶悬挂动作。

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