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伴有脑桥上部和/或中脑病变的外展轻瘫:假性展神经麻痹及其与所谓的卢茨后核间性眼肌麻痹的关系。

Abduction paresis with rostral pontine and/or mesencephalic lesions: Pseudoabducens palsy and its relation to the so-called posterior internuclear ophthalmoplegia of Lutz.

作者信息

Thömke F, Hopf H C

机构信息

Deparment of Neurology, University of Mainz, Mainz, Germany.

出版信息

BMC Neurol. 2001 Dec 18;1:4. doi: 10.1186/1471-2377-1-4.

Abstract

BACKGROUND

The existence of a prenuclear abduction paresis is still debated.

METHODS

In a retrospective design, we identified 22 patients with isolated unilateral (n = 20) or bilateral (n = 2) abduction paresis and electrophysiologic abnormalities indicating rostral pontine and/or mesencephalic lesions. Another 11 patients had unilateral abduction paresis with additional ocular motor abnormalities indicating midbrain dysfunction. Eight of these 11 patients also had electrophysiological abnormalities supporting this location. Electrophysiological examinations in all patients included masseter and blink reflexes (MassR, BlinkR), brainstem auditory evoked potentials (BAEP), and direct current elctro-oculography (EOG).

RESULTS

Unilateral MassR abnormalities in patients with unilateral abduction paresis were seen in 17 patients and were almost always (in 16 of 17 patients) on the side of the abduction paresis. Another 11 patients had bilateral MassR abnormalities. BlinkR was always normal. EOG disclosed slowed abduction saccades in the non-paretic eye in 6 patients and slowed saccades to the side opposite to the abduction paresis in another 5 patients. Re-examinations were done in 27 patients showing normalization or improvement of masseter reflex abnormalities in 18 of 20 patients and in all patients with EOG abnormalities. This was always associated with clinical improvement.

CONCLUSIONS

Electrophysiologically documented or clinically evident rostral pontine and/or mesencephalic lesions in our patients exclude an infranuclear intrapontine 6th nerve lesion and indicate the existence of an abduction paresis of prenuclear origin. An increased tone of the antagonistic medial rectus muscle during lateral gaze either by abnormal convergence or impaired medial rectus inhibition seems most likely.

摘要

背景

核前外展性轻瘫的存在仍存在争议。

方法

采用回顾性研究设计,我们确定了22例孤立性单侧(n = 20)或双侧(n = 2)外展性轻瘫且伴有电生理异常提示脑桥上部和/或中脑病变的患者。另外11例患者有单侧外展性轻瘫并伴有其他眼动异常提示中脑功能障碍。这11例患者中有8例也有支持该病变部位的电生理异常。所有患者的电生理检查包括咬肌反射和瞬目反射(MassR、BlinkR)、脑干听觉诱发电位(BAEP)以及直流电眼震图(EOG)。

结果

单侧外展性轻瘫患者中,17例出现单侧MassR异常,且几乎总是(17例中的16例)出现在外展性轻瘫侧。另外11例患者有双侧MassR异常。BlinkR总是正常。EOG显示6例患者非麻痹眼的外展扫视减慢,另外5例患者向与外展性轻瘫相反侧的扫视减慢。对27例患者进行了复查,结果显示20例患者中有18例咬肌反射异常恢复正常或改善,所有EOG异常的患者也有改善。这总是与临床症状改善相关。

结论

我们患者中电生理记录或临床明显的脑桥上部和/或中脑病变排除了脑桥核内第6神经核下病变,并提示存在核前起源的外展性轻瘫。在侧方凝视时,由于异常集合或内侧直肌抑制受损导致拮抗肌内侧直肌张力增加似乎是最可能的原因。

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