格林-巴利综合征与重症肌无力的巧合

Q4 Immunology and Microbiology
Majed Alluqmani
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引用次数: 0

摘要

格林-巴利综合征(GBS)和重症肌无力(MG)在同一个体中同时发生的情况很少见。该病例的潜在病理生理学被认为是自身免疫性体液机制。分子拟态,即自身抗体与外周神经髓鞘和神经肌肉接头乙酰胆碱受体之间发生交叉反应,不能排除为潜在原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The coincidence of Guillain-Barré syndrome and myasthenia gravis

Background

The occurrence of both Guillain-Barré syndrome (GBS) and myasthenia gravis (MG) in the same individual is rare. The underlying pathophysiology of this case was assumed to be an autoimmune humoral mechanism. Molecular mimicry, in which a cross-reaction occurs between autoantibodies and the myelin sheath of peripheral nerves and acetylcholine receptors of the neuromuscular junction, cannot be excluded as an underlying cause.

Case presentation

An 18-year-old female presented with symptoms of generalized weakness and distal weakness in both upper and lower extremities, more pronounced on the right side, and with associated right foot drop and bilateral ptosis. An electrophysiological study was performed and the acetylcholine receptor antibody titer determined. The patient was diagnosed with GBS and MG.

Conclusions

GBS and MG are two different neurological entities with different pathophysiologies. New-onset or persistence of symptoms in a patient with GBS treated with intravenous immunoglobulins or plasmapheresis should prompt a probe for another autoimmune neurological illness, particularly autoimmune neuromuscular disorders such as MG.

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来源期刊
Clinical and Experimental Neuroimmunology
Clinical and Experimental Neuroimmunology Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
1.60
自引率
0.00%
发文量
52
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