A case of brachial multisegmental amyotrophy caused by spontaneous spinal cerebrospinal fluid leak leading to epidural fluid collection

Atsuhiko Sugiyama , Ado Tamiya , Hajime Yokota , Hiroki Mukai , Hiroshi Amino , Satoshi Kuwabara
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引用次数: 0

Abstract

A 68-year-old man suffered from slowly progressive proximal upper extremity weakness for 17 years. Examination revealed bilateral C5–C6 muscle weakness. Upon spinal magnetic resonance imaging (MRI), the T2-weighted images showed high-intensity signals in the anterior horns at the C3–C5 spinal levels, with ventral epidural fluid collection at the C6–T6 spinal levels. Brain MRI also revealed hemosiderin deposition in the cerebellum. The patient was ultimately diagnosed with brachial multisegmental amyotrophy caused by spontaneous spinal cerebrospinal fluid leak with superficial siderosis. During surgery, a dural defect was identified at the T2–T3 spinal level, which was subsequently repaired. At the 60-month follow-up, no signs of disease progression were noted. This disease could potentially be treated through surgery and should be included in the differential diagnosis of slowly progressive segmental amyotrophy.

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一例自发性脊髓脑脊液漏导致硬膜外积液引起的肱骨多节段肌萎缩症病例
一名 68 岁的男子患有缓慢进行性上肢近端无力 17 年。检查发现双侧 C5-C6 肌肉无力。脊柱磁共振成像(MRI)显示,T2加权图像显示C3-C5脊柱前角有高强度信号,C6-T6脊柱腹侧硬膜外积液。脑磁共振成像还显示小脑有血色素沉积。患者最终被诊断为肱骨多节段肌萎缩症,由自发性脊髓脑脊液漏和浅层蛛网膜病变引起。手术中发现 T2-T3 脊柱硬膜缺损,随后进行了修复。在 60 个月的随访中,没有发现疾病进展的迹象。这种疾病有可能通过手术治疗,应将其纳入缓慢进行性节段性肌萎缩症的鉴别诊断中。
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CiteScore
1.00
自引率
0.00%
发文量
236
审稿时长
15 weeks
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