Subacute Upper Motor Neuron Dysfunction Possibly Associated with the Anti-GM1 Autoantibody

Anti-GM1 antibodies are associated with Guillain-Barré syndrome (GBS), primarily peripheral neuropathy. However, there are cases of anti-GM1 IgG antibody-positive GBS with upper motor neuron (UMN) signs. We herein report a case of gastrointestinal infection followed by subacute gait disturbance with predominant signs of UMN on a neurological examination. The serum and cerebrospinal fluid tests were positive for anti-GM1 and anti-asialo-GM1 IgG antibodies. An electrophysiological evaluation revealed normal nerve conduction and prolonged central motor conduction times. No magnetic resonance imaging abnormalities were observed. The symptoms improved with treatment, which was accompanied by decreased antibody titers. This case highlights the fact that anti-GM1 IgG-associated disorders may present with predominant UMN involvement.

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Publication Details

Journal
Internal Medicine
Published
2024-11-27
DOI
https://doi.org/10.2169/internalmedicine.4667-24
Citations
2
Primary Topic
Peripheral Neuropathies and Disorders
Type
article
Field-Weighted Citation Impact
0.74

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article

Subacute Upper Motor Neuron Dysfunction Possibly Associated with the Anti-GM1 Autoantibody

Hiroyuki Ishiura, Meiko Hashimoto Maeda, Masashi Hamada, Tatsushi Toda et al.
2 citations
Internal Medicine
Peripheral Neuropathies and Disorders
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article

Subacute Upper Motor Neuron Dysfunction Possibly Associated with the Anti-GM1 Autoantibody

Hiroyuki Ishiura, Meiko Hashimoto Maeda, Masashi Hamada, Tatsushi Toda, Kazuto Katsuse, Wataru Satake, S Okubo, Yuichiro Shirota
article en
2 citations

Abstract

Anti-GM1 antibodies are associated with Guillain-Barré syndrome (GBS), primarily peripheral neuropathy. However, there are cases of anti-GM1 IgG antibody-positive GBS with upper motor neuron (UMN) signs. We herein report a case of gastrointestinal infection followed by subacute gait disturbance with predominant signs of UMN on a neurological examination. The serum and cerebrospinal fluid tests were positive for anti-GM1 and anti-asialo-GM1 IgG antibodies. An electrophysiological evaluation revealed normal nerve conduction and prolonged central motor conduction times. No magnetic resonance imaging abnormalities were observed. The symptoms improved with treatment, which was accompanied by decreased antibody titers. This case highlights the fact that anti-GM1 IgG-associated disorders may present with predominant UMN involvement.

Internal MedicineVol. 64(12)
Okayama University (JP), University of Tokyo Hospital (JP), The University of Tokyo (JP)
Japan Agency for Medical Research and Development, Ministry of Health, Labour and Welfare
Openalex Percentile: Top 25%
Peripheral Neuropathies and Disorders
0.74
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