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颈后动脉壁动脉瘤导致的假性肌无力:一种新的表现形式:病例报告

Pseudomyasthenia resulting from a posterior carotid artery wall aneurysm: a novel presentation: case report.

作者信息

Tummala R P, Harrison A, Madison M T, Nussbaum E S

机构信息

Department of Neurosurgery, University of Minnesota School of Medicine, Minneapolis, Minnesota.

出版信息

Neurosurgery. 2001 Dec;49(6):1466-8; discussion 1468-9. doi: 10.1097/00006123-200112000-00034.

Abstract

OBJECTIVE AND IMPORTANCE

Painful oculomotor palsy can result from enlargement or rupture of intracranial aneurysms. The IIIrd cranial nerve dysfunction in this setting, whether partial or complete, is usually fixed or progressive and is sometimes reversible with surgery. We report an unusual oculomotor manifestation of a posterior carotid artery wall aneurysm, which mimicked ocular myasthenia gravis.

CLINICAL PRESENTATION

A 47-year-old woman developed painless, intermittent, partial IIIrd cranial nerve palsy. She presented with isolated episodic left-sided ptosis, which initially suggested a metabolic or neuromuscular disorder. However, digital subtraction angiography revealed a left posterior carotid artery wall aneurysm, just proximal to the origin of the posterior communicating artery.

INTERVENTION

The aneurysm was successfully clipped via a pterional craniotomy. During surgery, the aneurysm was observed to be compressing the oculomotor nerve. The patient's symptoms resolved after the operation.

CONCLUSION

The variability of incomplete IIIrd cranial nerve deficits can present a diagnostic challenge, and the approach for patients with isolated IIIrd cranial nerve palsies remains controversial. Although intracranial aneurysms compressing the oculomotor nerve classically produce fixed or progressive IIIrd cranial nerve palsies with pupillary involvement, anatomic variations may result in atypical presentations. With the exception of patients who present with pupil-sparing but otherwise complete IIIrd cranial nerve palsy, clinicians should always consider an intracranial aneurysm when confronted with even subtle dysfunction of the oculomotor nerve.

摘要

目的及重要性

疼痛性动眼神经麻痹可由颅内动脉瘤扩大或破裂引起。在此情况下,动眼神经功能障碍,无论部分还是完全性,通常是固定的或进行性的,有时手术可使其逆转。我们报告一例颈内动脉后壁动脉瘤的不寻常动眼神经表现,其酷似眼肌型重症肌无力。

临床表现

一名47岁女性出现无痛性、间歇性、部分性动眼神经麻痹。她表现为孤立性发作性左侧上睑下垂,最初提示代谢或神经肌肉疾病。然而,数字减影血管造影显示左侧颈内动脉后壁动脉瘤,位于后交通动脉起始部近端。

干预措施

通过翼点开颅术成功夹闭动脉瘤。手术中观察到动脉瘤压迫动眼神经。术后患者症状消失。

结论

不完全性动眼神经缺损的变异性可能带来诊断挑战,孤立性动眼神经麻痹患者的治疗方法仍存在争议。尽管压迫动眼神经的颅内动脉瘤通常会导致伴有瞳孔受累的固定性或进行性动眼神经麻痹,但解剖变异可能导致非典型表现。除了表现为瞳孔保留但其他方面为完全性动眼神经麻痹的患者外,临床医生在面对即使是轻微的动眼神经功能障碍时,都应始终考虑颅内动脉瘤的可能。

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