[抗神经节苷脂抗体阳性格林-巴罗综合征伴不对称肌无力1例]。

Q4 Medicine
Clinical Neurology Pub Date : 2025-01-29 Epub Date: 2024-12-18 DOI:10.5692/clinicalneurol.cn-002001
Hitomi Sato, Rena Okudera, Yu Hongo, Taro Matsui, Katsunori Ikewaki, Kazushi Suzuki
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引用次数: 0

摘要

56岁女性,腹泻一周后出现左下垂足和腰痛。神经系统症状持续一周后逐渐改善。在疾病过程中,上肢未见无力,左下肢明显不对称肌无力。神经传导研究显示左侧胫骨和腓骨神经运动反应缺失,右侧胫骨神经复合肌动作电位振幅下降,但传导不减慢。血清IgG抗galnac - gd1a抗体和抗神经节苷复合物抗体阳性。基于这些发现,我们诊断她为一种罕见的格林-巴罗综合征(GBS),伴有明显的不对称肌肉无力。在文献中,伴有不对称肌无力的GBS患者通常具有与急性运动轴索神经病变相关的抗神经节苷脂抗体。详细的病史记录和临床病程信息有助于准确诊断伴有非典型虚弱分布的GBS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A case of anti-ganglioside antibody-positive Guillain-Barré syndrome with asymmetrical muscle weakness throughout the course of the disease].

A 56-year-old woman who presented with left drop foot and low back pain a week after the onset of diarrhea. Neurological symptoms progressed for a week and gradually improved thereafter. No weakness was observed in upper limbs and clearly asymmetrical muscle weakness was observed in left lower limbs during the course of the disease. Nerve conduction study demonstrated absent motor responses in the left tibial and fibular nerves, and compound muscle action potentials in the right tibial nerve was decreased in amplitude without conduction slowing. Serum IgG anti-GalNAc-GD1a antibody and anti-ganglioside complex antibodies were positive. Based on these findings, we diagnosed her as a rare variant of Guillain-Barré syndrome (GBS) with marked asymmetrical muscle weakness. In the literature, GBS patients with asymmetrical muscle weakness often have anti-ganglioside antibodies associated with acute motor axonal neuropathy. A detailed history taking and information on the clinical course are helpful for accurate diagnosis of GBS with atypical distribution of weakness.

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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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