格林-巴利综合征与布鲁氏菌病:1例报告和文献回顾

S. Daoud, N. Farhat, H. Kacem, O. Hdiji, S. Sakka, M. Damak, Chokri Mhir
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引用次数: 1

摘要

格林-巴利综合征(GBS)是世界上导致急性弛缓性麻痹的最常见原因。它是一种自身免疫性多根神经病变,通常在急性感染之前发生。很少,布鲁氏菌病可诱发GBS。目的:探讨布鲁氏菌所致GBS的临床及微生物学诊断特点。病例报告:一名54岁女性,无既往病史,于传染病科随访。她被诊断患有布鲁氏菌病。她接受了抗生素治疗(利福平600毫克/天,强力霉素200毫克/天)。治疗4天后,患者因面部肌肉快速进行性、上升性、对称性无力及双侧麻痹转至我科。入院时,她很警觉。所有四肢均无深肌腱反射(DTRs)。上肢肌力3/5,下肢肌力2/5。下肢本体感觉受损,但她没有任何感觉问题。我们的病人还表现出面部双瘫。体格检查正常,除脾肿大外。腰椎穿刺显示脑脊液白蛋白细胞学分离。神经传导检查提示脱髓鞘性多根神经病变。库姆斯赖特滴定为1/160。讨论:由于诊断为GBS并伴有布鲁氏菌病,我们的患者接受了抗生素治疗(利福平600毫克/天,强力霉素200毫克/天)。在住院期间,她进行了四次血浆置换和一次运动康复。在4周后的随访中,我们的患者出现了部分恢复,并且她能够在没有支持的情况下行走。结论:本病例表明布鲁氏菌病可表现为罕见的神经系统表现,包括GBS。分子模仿似乎是导致这种并发症的原因,通过合成针对髓鞘神经节苷的自身抗体。因此,所有出现急性弛缓性麻痹的患者,特别是生活在流行地区的患者,都应排除布鲁氏菌病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Guillain Barre Syndrome Associated with Brucellosis: A Case Report and Review of the Literature
Introduction: Guillain-Barre syndrome (GBS) ranks as the most frequent cause of acute flaccid paralysis in the world. It is an autoimmune polyradiculoneuropathy, usually preceded by an acute infection. Rarely, brucellosis may induce a GBS.Objective: To evaluate the clinical and microbiological diagnostic properties of Brucella-induced GBS.Case Report: A 54-year-old woman, with no past medical history, was followed in infectious disease department. She was diagnosed with brucellosis. She had received antibiotic therapy (Rifampicin 600 mg/day and Doxycycline 200 mg/day). After 4 days of treatment, she was referred to our department because of rapidly progressive, ascending, symmetric weakness and bilateral paralysis of muscles of the face. On admission, she was alert. The deep tendon reflexes (DTRs) were absent in all extremities. Muscle strength was 3/5 in the upper extremities and 2/5 in the lower extremities. Proprioception in the lower extremities was impaired, but she did not have any sensory problems. Our patient also presented a facial diplegia. Physical examination was normal, except for splenomegaly. A lumbar puncture showed an albumin-cytologic dissociation in the CSF. Nerve-conduction studies were suggestive of demyelinating polyradiculoneuropathy. Coombs Wright titration was 1/160..Discussion: With a diagnosis GBS preceded by brucellosis, our patient was given an antibiotic therapy (Rifampicin 600 mg/day and Doxycycline 200 mg/day). During hospitalization, she had four plasma exchange sessions and a motor rehabilitation. In a follow-up after 4 weeks, our patient presented a partial recovery, and she was able to walk without support.Conclusion: This case demonstrates that brucellosis can present with a rare neurologic manifestation including GBS. Molecular mimicry seems to be responsible for this complication, through the synthesis of autoantibodies against myelin gangliosides. Thus, brucellosis should be ruled out in all patients who develop acute flaccid paralysis, especially in those who live in endemic areas.
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