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一例最初表现为吉兰-巴雷综合征的背侧硬膜外椎间盘突出碎片

A Dorsal Epidural Herniated Disc Fragment Initially Presenting as Guillain-Barré Syndrome.

作者信息

Patel Parth N, Schloss Michael G, Sharma Kaveri, Dulai Poonam

机构信息

Physical Medicine and Rehabilitation, Mercy Hospital, Catholic Health, Rockville Centre, USA.

Neurology, Mercy Hospital, Catholic Health, Rockville Centre, USA.

出版信息

Cureus. 2022 Jun 7;14(6):e25719. doi: 10.7759/cureus.25719. eCollection 2022 Jun.

Abstract

Guillain-Barré syndrome (GBS) is a rare autoimmune disorder that presents with neurological symptoms that can mimic other conditions. This mimicry can hide other important neurological diagnoses. Here, we present a rare case of thoracic myelopathy secondary to a sequestered dorsal epidural herniated disc fragment that initially presented with the classic findings of GBS. A 58-year-old female presented with progressing bilateral lower extremity weakness, paresthesias, and absent bilateral lower extremity deep tendon reflexes. Lumbar magnetic resonance imaging (MRI) findings were disproportionate to presentation, and lumbar puncture fluid analysis revealed clear, colorless fluid with albuminocytological dissociation. The patient was diagnosed with GBS and treated with a short course of intravenous steroids followed by intravenous immunoglobulin. The patient later developed new-onset ulnar distribution paresthesias, lower extremity spasticity, constipation, and urinary retention that caused a decline in functional progress. Further investigation prompted evaluation with cervical and thoracic MRIs, which revealed a left dorsal epidural lesion at the T9-T10 level causing severe cord compression. The patient was definitively treated with a T9-T10 laminectomy and excision of the offending lesion. Pathology revealed collagenous tissue with fibroblastic proliferation, consistent with a sequestered fragment of the herniated intervertebral disc. The patient was further treated with both acute and subacute rehabilitation. She was eventually discharged home and was able to ambulate independently with a walker. Dependency on positive albuminocytological dissociation in cases of potential GBS can lead to errors in diagnostic accuracy and delay appropriate treatment. Clinicians should remain mindful that GBS is a diagnosis of exclusion and MRI of the entire spine should be considered when the diagnosis of GBS is uncertain.

摘要

吉兰 - 巴雷综合征(GBS)是一种罕见的自身免疫性疾病,其神经系统症状可能与其他病症相似。这种相似性可能掩盖其他重要的神经系统诊断。在此,我们报告一例罕见的因隐匿性背侧硬膜外椎间盘突出碎片继发的胸段脊髓病,该病例最初表现为吉兰 - 巴雷综合征的典型症状。一名58岁女性出现双侧下肢进行性无力、感觉异常,双侧下肢深腱反射消失。腰椎磁共振成像(MRI)结果与临床表现不符,腰椎穿刺脑脊液分析显示清亮、无色液体,存在蛋白细胞分离现象。该患者被诊断为吉兰 - 巴雷综合征,并接受了短期静脉注射类固醇治疗,随后静脉注射免疫球蛋白。患者后来出现新发的尺侧感觉异常、下肢痉挛、便秘和尿潴留,导致功能进展下降。进一步检查促使进行颈椎和胸椎MRI评估,结果显示T9 - T10水平左侧硬膜外病变,导致严重脊髓受压环。患者最终接受了T9 - T10椎板切除术并切除病变。病理显示胶原组织伴有成纤维细胞增生,符合椎间盘突出的隐匿性碎片。患者进一步接受了急性和亚急性康复治疗。她最终出院回家,能够借助助行器独立行走。在潜在吉兰 - 巴雷综合征病例中依赖阳性蛋白细胞分离可能导致诊断准确性错误并延误适当治疗。临床医生应牢记,吉兰 - 巴雷综合征是一种排除性诊断,当吉兰 - 巴雷综合征诊断不确定时,应考虑对整个脊柱进行MRI检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae7f/9261972/ee078433c74b/cureus-0014-00000025719-i01.jpg

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