快速进展的广泛性多发性颅神经病变是格林-巴利综合征的一种变体:一例报告

Q4 Medicine
Joselyn Miño , Alejandra Heriz , Rodrigo Sanjinez , Rocío Márquez , Juan Pablo Rodríguez , Otto Vega , José Zuñiga , Marcelo Rugiero
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引用次数: 0

摘要

格林-巴勒综合征的临床表现可能是异质的,因为它有多种变体,一些是明确的,另一些是疾病谱系的一部分。临床病例:35岁女性,表现为多发性颅神经病变,无其他表现。测定脑脊液中GD1b和GQ1b阳性的抗神经节苷脂抗体。丙种球蛋白治疗效果良好。结论吉兰-巴罗变异体可发生多发性颅神经病变,就本病例而言,GD1b和GQ1b抗体的分布可解释患者的临床表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuropatía craneana múltiple extensa rápidamente progresiva como variante de síndrome de Guillain-Barré: reporte de un caso

Introduction

The clinical presentation of Guillain-Barré syndrome can be heterogeneous due to its multiple variants, some defined and others that are part of the spectrum of the disease.

Clinical case

Thirty-five-year-old female who presented with multiple cranial neuropathy, with no other findings. Determination of antiganglioside antibodies in cerebrospinal fluid, positive for GD1b and GQ1b, was performed. Treatment with gamma globulin was performed with good response.

Conclusion

Multiple cranial neuropathy can occur in the context of Guillain-Barré variants, in relation to the case presented, the distribution of GD1b and GQ1b antibodies would explain the clinical presentation of the patient.

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来源期刊
Neurologia Argentina
Neurologia Argentina Medicine-Neurology (clinical)
CiteScore
0.50
自引率
0.00%
发文量
34
期刊介绍: Neurología Argentina es la publicación oficial de la Sociedad Neurológica Argentina. Todos los artículos, publicados en español, son sometidos a un proceso de revisión sobre ciego por pares con la finalidad de ofrecer información original, relevante y de alta calidad que abarca todos los aspectos de la Neurología y la Neurociencia.
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