Guillian-Barré Syndrome with multiple cranial neuropathies

Chandra Wirawan, Ni Made Dwita Pratiwi, I Komang Arimbawa, I Wayan Widyantara
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Abstract

Background. Guillain-Barré Syndrome (GBS) is an autoimmune reaction against peripheral nerves that manifests clinically as acute polyradiculoneuropathy. Classic sensory-motor, pure motor, paraparesis, pharyngeal-cervical-brachial, Bickerstaff brainstem encephalitis, pure sensory, bilateral facial palsy with paresthesia, and Miller-Fisher syndrome are all known variants of GBS. This case report seeks to describe a case of GBS with involvement of the cranial nerves. Case report. A 39-year-old right-handed Balinese woman presented with LMN (Lower Motor Neuron) type paraparesis with ascending paralysis and involvement of cranial nerves III through XII. The results of the LCS (Liquor Cerebro-Spinal) demonstrate albuminocytological dissociation. According to the patient’s EMNG (electromyoneurography) findings, Guillain-Barré Syndrome was of the AMAN (acute motor axonal neuropathy) variety. The patient was diagnosed with multiple cranial neuropathies and GBS of the AMAN type. EGRIS (Erasmus GBS Respiratory Insufficiency Score) was 3, and EGOS (Erasmus GBS Obstructive Sleep Apnea Score) was also 3. Following IVIG (Intravenous Immunoglobulin) treatment, the patient exhibited clinical improvement (Hughes score decreased from 4 to 2). Discussion. The patient exhibits clinical manifestations of flaccid tetraparesis and multiple cranial nerve paresis. The clinical condition of the patient did not meet the criteria for GBS clinical variation. Symptoms of flaccid tetraparesis that do not involve the senses are classified as the motor-only variant. This patient’s differential diagnosis includes the possibility of MFS and ophthalmoplegia. This patient, however, had flaccid tetraparesis and no ataxia. Electromyoneurography (EMNG) examination produces AMAN-type GBS. The patient was diagnosed with one of the clinical variants of GBS, AMAN-type GBS with multiple cranial neuropathies. Conclusion. A case of GBS of the AMAN type accompanied by multiple cranial neuropathies has been reported.
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伴有多发性颅神经病变的格林-巴瑞综合征
背景。格林-巴罗综合征(GBS)是一种针对周围神经的自身免疫反应,临床表现为急性多神经根神经病变。典型的感觉-运动、纯运动、麻痹、咽-颈-臂、比克斯塔夫脑干脑炎、纯感觉、双侧面瘫伴感觉异常和米勒-费舍尔综合征都是已知的GBS变体。本病例报告旨在描述一例GBS与脑神经受累。病例报告。一位39岁的巴厘岛右撇子女性,表现为LMN(下运动神经元)型截瘫,并伴有上升性麻痹和脑神经III至XII受累。LCS(液体脑脊髓)结果显示白蛋白细胞学解离。根据患者的肌电神经图显示,格林-巴罗综合征属于急性运动轴索神经病(AMAN)类型。患者被诊断为多发性颅神经病变和AMAN型GBS。EGRIS (Erasmus GBS呼吸功能不全评分)为3分,EGOS (Erasmus GBS阻塞性睡眠呼吸暂停评分)为3分。在静脉注射免疫球蛋白治疗后,患者表现出临床改善(Hughes评分从4分下降到2分)。患者临床表现为弛缓性四肢瘫和多发性脑神经麻痹。患者临床情况不符合GBS临床变异标准。不涉及感官的弛缓性四瘫症状被归类为仅运动型四瘫。该患者的鉴别诊断包括MFS和眼麻痹的可能性。然而,该患者有弛缓性四全,无共济失调。肌电图(EMNG)检查产生aman型GBS。患者被诊断为GBS的临床变体之一,aman型GBS伴多发性颅脑神经病变。结论。本文报道1例AMAN型GBS伴多发性颅脑神经病变。
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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
30
审稿时长
4 weeks
期刊介绍: ROMANIAN JOURNAL OF NEUROLOGY (Revista Română de Neurologie), the official journal of the Romanian Society of Neurology, was founded in 2001, being a prestigious scientific journal that provides a high quality in terms of scientific content, but also the editorial and graphic aspect, both through an impartial process of selection, evaluation and correction of articles (peer review procedure), as well as providing editorial, graphic and printing conditions at the highest level. In order to increase the scientific standards of the journal, special attention was paid to the improvement of the quality of the published materials. Guidance articles, clinical trials and case studies are structured in several sections: reviews, original articles, case reports, images in neurology. All articles are published entirely in English. A team of reputable medical professionals in the field of neurology is involved in a rigorous peer review process that complies with international ethics and quality rules in the academic world.
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