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[真性神经型胸廓出口综合征]

[True neurological thoracic outlet syndrome].

作者信息

Le Forestier N, Mouton P, Maisonobe T, Fournier E, Moulonguet A, Willer J C, Bouche P

机构信息

Fédération d'explorations fonctionnelles neurologiques, Hôpital de la Salpêtrière, Paris.

出版信息

Rev Neurol (Paris). 2000 Jan;156(1):34-40.

Abstract

The thoracic outlet syndrome (TOS) encompasses various clinical entities affecting the neurovascular bundle crossing the thoracic outlet. Unfortunately, this term often proves to be confusing because many of these entities have little in common beyond their known or presumed lesion site. Neurogenic TOS (true TOS) is caused by compression of the lower trunk in the brachial plexus, the cervical ribs or fibrous band. This syndrome is extremely rare. We consider that this neurological form of TOS is a clearly defined neurological syndrome. We report 10 patients with true TOS. All were females. Stating the onset was difficult because symptoms were progressive and insidious. Pain was the most frequently reported symptom. Sensory deficit was slight or absent. All patients showed unilateral severe atrophy of the thenar muscles. Wasting and weakness developed later. A reduced amplitude of ulnar and median compound muscle action potential associated with a normal amplitude of median sensory nerve action and a reduced amplitude of ulnar sensory nerve action potential were indicative of a chronic axon loss in the lower trunk of the brachial plexus. In all cases, we performed medial antebrachial cutaneous sensory nerve action potential, a C8-T1 innervated nerve. The absence of the medial antebrachial cutaneous sensory nerve action potential in 9 patients and a reduction in amplitude of 50 p. 100 compared to the unaffected side in the other patient, indicated the diagnostic value of this easy and reproductible test. It confirmed a C8-T1 post-ganglionic radicular lesion or a lower brachial plexus neuropathy. Radiography showed a rudimentary bilateral cervical rib or an elongated C7 transverse process in all cases. Surgery was performed in the affected side in 7 patients and in each case the lower part of the brachial plexus was found to be stretched and angulated over a fibrous band, which was removed. Pain was relieved after 1 to 4 weeks. A minimal motor improvement was observed after one year. Electrophysiological results were unchanged.

摘要

胸廓出口综合征(TOS)包括多种影响穿过胸廓出口的神经血管束的临床病症。不幸的是,这个术语常常令人困惑,因为这些病症除了已知或推测的病变部位外,几乎没有共同之处。神经源性TOS(真性TOS)是由臂丛神经下干、颈肋或纤维带受压引起的。这种综合征极为罕见。我们认为这种神经学形式的TOS是一种明确界定的神经综合征。我们报告了10例真性TOS患者。均为女性。由于症状呈进行性且隐匿,很难说明发病情况。疼痛是最常报告的症状。感觉缺陷轻微或不存在。所有患者均表现为单侧大鱼际肌严重萎缩。萎缩和无力随后出现。尺神经和正中神经复合肌肉动作电位幅度降低,同时正中感觉神经动作电位幅度正常,尺神经感觉神经动作电位幅度降低,提示臂丛神经下干存在慢性轴突丢失。在所有病例中,我们都进行了前臂内侧皮感觉神经动作电位检测,这是一条由C8 - T1支配的神经。9例患者前臂内侧皮感觉神经动作电位缺失,另一例患者与未受影响侧相比幅度降低了50%,这表明了这项简单且可重复的检测的诊断价值。它证实了C8 - T1节后神经根病变或低位臂丛神经病变。X线检查显示所有病例均有双侧颈肋发育不全或C7横突过长。7例患者在患侧进行了手术,在每例手术中均发现臂丛神经下部在一条纤维带上被拉伸并成角,将该纤维带切除。1至4周后疼痛缓解。一年后观察到运动功能有轻微改善。电生理结果未改变。

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