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临床推理:一位 26 岁女性,慢性进行性步态功能障碍。

Clinical Reasoning: A 26-Year-Old Woman With Chronic Progressive Gait Dysfunction.

机构信息

From the Department of Neurology, University of Pennsylvania, Philadelphia.

出版信息

Neurology. 2024 Oct 8;103(7):e209830. doi: 10.1212/WNL.0000000000209830. Epub 2024 Sep 5.

Abstract

Careful evaluation of symptom progression and radiographic findings are essential tools when approaching cases of suspected chronic myelopathies. In this case, a 26-year-old woman presented with progressive ambulatory and bladder dysfunction for 4 years. Her examination was marked by bilateral lower-extremity upper motor neuron signs and distal large-fiber sensory loss. Neurologic workup for acquired causes of this presentation was unrevealing. MRI of the brain revealed a characteristic radiologic finding. Guided genetic testing ultimately yielded the final diagnosis. In this clinical vignette, we review the approach to chronic myelopathy including consideration of genetic etiologies and pursuit of targeted gene testing. We further discuss the typical clinical and radiographic findings of a rare diagnosis.

摘要

当遇到疑似慢性脊髓病的病例时,仔细评估症状进展和影像学发现是非常重要的工具。在本例中,一名 26 岁女性因进行性步行和膀胱功能障碍就诊 4 年。她的检查表现为双侧下肢上运动神经元体征和远端大纤维感觉丧失。针对这种表现的获得性病因的神经学检查结果无明显异常。脑部 MRI 显示出一种特征性的影像学发现。有针对性的基因检测最终得出了明确的诊断。在本临床病例中,我们回顾了慢性脊髓病的处理方法,包括考虑遗传病因和进行靶向基因检测。我们进一步讨论了这种罕见诊断的典型临床和影像学发现。

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本文引用的文献

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Disparities in Genetic Testing for Neurologic Disorders.神经疾病基因检测中的差异。
Neurology. 2024 Mar 26;102(6):e209161. doi: 10.1212/WNL.0000000000209161. Epub 2024 Mar 6.
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Clinical Approach to Myelopathy Diagnosis.脊髓病诊断的临床方法。
Continuum (Minneap Minn). 2024 Feb 1;30(1):14-52. doi: 10.1212/CON.0000000000001390.
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Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches.遗传性痉挛性截瘫:从诊断到新兴治疗方法。
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