伴有白蛋白细胞学分离的埃尔斯伯格综合征--吉兰-巴雷综合征的拟态还是吉兰-巴雷综合征的变异?

IF 0.9 Q4 CLINICAL NEUROLOGY Neurohospitalist Pub Date : 2024-07-01 Epub Date: 2024-02-20 DOI:10.1177/19418744241233621
Joseph M Ferrara, Courtney Litchmore, Smit Shah, Jeffery Myers, Khalil Ali
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引用次数: 0

摘要

导言:埃尔斯伯格综合征是一种推测为感染性的腰骶部神经根炎,伴有或不伴有腰髓炎,通常归因于单纯疱疹病毒 2 型(HSV-2):病例:一名 58 岁男子因下肢麻醉、共济失调步态、放射学证据显示患有根管炎和脑脊液白蛋白细胞学解离而就诊。脑脊液聚合酶链反应检测证实感染了 HSV-2:结论:埃尔斯伯格综合征的表现多种多样,可能具有不同的发病机制。皮疹消退后神经系统症状延迟出现,且无多形性红细胞增多症,这使得一些符合埃尔斯伯格综合征标准的患者可能患有感染后免疫介导的神经病。我们建议降低急性神经病变和白蛋白细胞学分离患者的疱疹病毒 PCR 检测阈值,尤其是早期骶骨受累的病例。
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Elsberg Syndrome With Albuminocytologic Dissociation - A Guillain-Barré Syndrome Mimic or Guillain-Barré Syndrome Variant?

Introduction: Elsberg Syndrome is a presumed infectious lumbosacral radiculitis, with or without accompanying lumbar myelitis, that is often attributed to herpes simplex virus type 2 (HSV-2).

Case: A 58-year-old man presented with lower extremity anesthesia, ataxic gait, radiological evidence of radiculitis, and CSF albuminocytologic dissociation. Polymerase chain reaction testing of CSF confirmed HSV-2 infection.

Conclusion: A variety of presentations are reported within the scope of Elsberg Syndrome, potentially with distinct disease mechanisms. Delayed onset of neurological symptoms after resolution of rash and absence of pleocytosis raises the possibility that some patients meeting criteria for Elsberg Syndrome have a post-infectious immune-mediated neuropathy. We advise a lower threshold for PCR testing of herpes viruses in patients with acute neuropathy and albuminocytologic dissociation, particularly in cases with early sacral involvement.

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来源期刊
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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