Neurosyphilis Manifesting as a Longitudinally Extensive Transverse Myelitis: A Case Report.

IF 0.9 Q4 CLINICAL NEUROLOGY Neurohospitalist Pub Date : 2024-10-01 Epub Date: 2024-05-30 DOI:10.1177/19418744241258694
Gabriela A Bou, Qasem N AlShaer, Taylor B Harrison, Spencer K Hutto
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Abstract

Background: Evaluating patients with ascending sensorimotor deficits has a broad differential diagnosis at initial presentation which can be further narrowed upon neurologic examination but may represent a diagnostic and therapeutic dilemma in light of findings raising suspicion for multiple possible etiologies. Data Collection: In this case, a 29-year-old patient presented with ascending bilateral lower extremity sensory loss, paresthesias, and weakness which progressed to the inability to ambulate. Conclusions: This case highlights the diagnostic approach to patients with bilateral lower extremity sensorimotor deficits, discusses the development of a comprehensive differential diagnosis, and further evaluates the most likely etiologies. Furthermore, this case reviews complexities related to clinical reasoning in the setting of diagnostic uncertainty, particularly when the neurologic structures affected portend high risk for severe disability and early treatment may improve outcome.

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表现为纵向扩展性横贯性脊髓炎的神经梅毒:病例报告
背景:评估有上升性感觉运动障碍的患者,在初次就诊时需要进行广泛的鉴别诊断,在进行神经系统检查后可进一步缩小诊断范围,但由于检查结果令人怀疑可能存在多种病因,因此可能会造成诊断和治疗上的困境。数据收集:在本病例中,一名 29 岁的患者出现双侧下肢上升性感觉缺失、麻痹和无力,随后发展到无法行走。结论:本病例强调了对双侧下肢感觉运动障碍患者的诊断方法,讨论了综合鉴别诊断的发展,并进一步评估了最可能的病因。此外,本病例还回顾了在诊断不确定的情况下进行临床推理的复杂性,尤其是在受影响的神经结构预示着严重残疾的高风险以及早期治疗可能改善预后的情况下。
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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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