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格林-巴利综合征米勒-费雪变异型中的神经超声检查

Nerve ultrasound in Miller Fisher variant of Guillain-Barré syndrome.

作者信息

Décard Bernhard F, Fladt Joachim, Axer Hubertus, Fischer Dirk, Grimm Alexander

机构信息

Department of Neurology, Basel University Hospital, Petersgraben 4, CH-4031, Basel, Switzerland.

Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.

出版信息

Muscle Nerve. 2015 Dec;52(6):1106-10. doi: 10.1002/mus.24753. Epub 2015 Jul 24.

Abstract

INTRODUCTION

Focal enlargement of the peripheral and spinal nerves, visualized using high-resolution ultrasound (HRUS), has been reported in early Guillain-Barré syndrome, but not in the Miller Fisher variant. We report the use of HRUS in 2 patients who presented with acute ataxic neuropathy, areflexia, and ophthalmoparesis.

METHODS

Ultrasound and/or nerve conduction studies (NCS) of peripheral nerves, the vagus, and spinal nerves C5/6 were performed at onset and 2 weeks after immunoglobulin therapy.

RESULTS

Both patients fulfilled criteria for diagnosis of Miller Fisher syndrome (MFS). Laboratory findings revealed elevated ganglioside Q1b antibodies in both and an albuminolocytologic dissociation in 1 patient. In addition, 1 patient had NCS evidence for demyelinating neuropathy. However, ultrasound showed focal enlargement in the vagus, the spinal nerves, and/or in the peripheral nerves in both patients. After therapy, nerve enlargement decreased in parallel with clinical improvement.

CONCLUSION

Spinal and/or peripheral nerve enlargement supports the diagnosis of MFS in early phases of the disease.

摘要

引言

据报道,在早期吉兰 - 巴雷综合征中可通过高分辨率超声(HRUS)观察到周围神经和脊神经的局灶性增粗,但在米勒 - 费希尔变异型中未见此现象。我们报告了对2例表现为急性共济失调性神经病、无反射和眼肌麻痹患者使用HRUS的情况。

方法

在发病时以及免疫球蛋白治疗2周后,对周围神经、迷走神经和颈5/6脊神经进行超声和/或神经传导研究(NCS)。

结果

2例患者均符合米勒 - 费希尔综合征(MFS)的诊断标准。实验室检查结果显示,2例患者的神经节苷脂Q1b抗体均升高,1例患者存在蛋白细胞分离现象。此外,1例患者的NCS有脱髓鞘性神经病的证据。然而,超声显示2例患者的迷走神经、脊神经和/或周围神经均有局灶性增粗。治疗后,神经增粗程度与临床改善情况平行下降。

结论

脊髓和/或周围神经增粗有助于支持疾病早期MFS的诊断。

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