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头颈部患者多间隙深部筋膜感染并发吉兰-巴雷综合征:病例报告及文献复习

MultiSpace Deep Fascial Infection in the Head and Neck Patient Complicated with Guillain-Barre Syndrome: Case Report with a Literature Review.

作者信息

Fan Fengxia, Ni Hongli, Luo Wanjie, Yi Qingchuan

机构信息

Department of Otolaryngology, Head & Neck Surgery, Zigong Fourth People's Hospital, Zigong, Sichuan, China.

出版信息

Ear Nose Throat J. 2025 Jan 6:1455613241310290. doi: 10.1177/01455613241310290.

Abstract

Guillain-Barre syndrome (GBS) is the most prevalent and severe form of acute paralytic neuropathy, commonly triggered by infections and characterized by an abnormal autoimmune response. Reports of multispace deep fascial infection (DFI) in the head and neck complicated by GBS are exceedingly rare. We report a 69-year-old woman with DFI who developed postoperative limbs weakness. GBS was diagnosed after neurology consultation and cerebrospinal fluid (CSF) puncture examination. Then the patient was treated with intravenous immunoglobulin, as well as supportive care and rehabilitation exercise. After our treatment, the patient was discharged successfully. GBS is a rare complication after head and neck surgery. When progressive weakness occurs in patient of DFI, the possibility of GBS should be considered, and CSF and electrophysiological examinations should be performed as soon as possible. For patients with DFI complicated with GBS, prognosis depends on early diagnosis and treatment.

摘要

吉兰-巴雷综合征(GBS)是急性麻痹性神经病最常见、最严重的形式,通常由感染引发,其特征为异常的自身免疫反应。头颈部多间隙深部筋膜感染(DFI)并发GBS的报道极为罕见。我们报告一例69岁患有DFI的女性患者,术后出现肢体无力。经神经科会诊及脑脊液(CSF)穿刺检查后诊断为GBS。随后患者接受静脉注射免疫球蛋白治疗,以及支持性护理和康复锻炼。经过我们的治疗,患者成功出院。GBS是头颈外科手术后罕见的并发症。当DFI患者出现进行性无力时,应考虑GBS的可能性,并应尽快进行脑脊液和电生理检查。对于DFI合并GBS的患者,预后取决于早期诊断和治疗。

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