Chiari malformation type I with cervicothoracic syringomyelia masquerading as bibrachial amyotrophy: a case report

Jeffrey R Mora; Richard A Rison; Said R Beydoun

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Chiari malformation type I with cervicothoracic syringomyelia masquerading as bibrachial amyotrophy: a case report

机译：伪装为双臂肌萎缩的颈胸椎型脊髓空洞症的Chiari畸形I型：一例报告

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Introduction Clinical presentation of syringomyelia can mimic a variety of neuromuscular disorders. A misdiagnosis can result in progressive pressure on the spinal cord, causing the development of severe irreversible neurologic deficits. Case presentation We report the very unusual case of a 50-year-old Latino man who developed severe distal muscle atrophy and bulbar dysfunction as a result of Chiari malformation type I with chronic cervicothoracic syringomyelia. Conclusion Syringomyelia is a potentially serious neurologic condition with symptoms that can mimic other neuromuscular disorders. Severe untreated cases can result in irreversible spinal cord injury. Prompt diagnosis with magnetic resonance imaging is important in both establishing diagnosis and directing further surgical management.

机译：简介脊髓空洞症的临床表现可模拟多种神经肌肉疾病。误诊会导致脊髓进行性压力，导致严重的不可逆神经功能缺损。病例介绍我们报告了一个非常不寻常的病例，该病例是一名50岁的拉丁美洲人，由于患有I型Chiari畸形并伴有慢性颈胸腔脊髓脊髓空洞症而导致严重的远端肌肉萎缩和延髓功能障碍。结论脊髓空洞症是一种潜在的严重神经系统疾病，其症状可模仿其他神经肌肉疾病。严重的未经治疗的病例可导致不可逆转的脊髓损伤。借助磁共振成像的及时诊断对于建立诊断和指导进一步的手术管理都很重要。

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《Journal of Medical Case Reports》 |2015年第3期|共页
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Jeffrey R Mora; Richard A Rison; Said R Beydoun;
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机译：Chiari I型畸形伴颈胸脊髓脊髓空洞症fl臂综合征
2. A rare case of Chiari type-1 malformation accompanied by symptomatic cerebrospinal fluid hypovolemia: Comparison of congenital Chiari type-1 malformation and acquired Chiari malformation secondary to cerebrospinal fluid hypovolemia: Case report [J] . HataeR., KohriR., MaedaK., Neurologia medico-chirurgica. . 2014,第7期

机译：罕见的Chiari 1型畸形伴有症状性脑脊液血容量不足的病例：先天性Chiari 1型畸形与继发于脑脊液血容量不足的获得性Chiari畸形的比较：病例报告
3. A Rare Case of Chiari Type-1 Malformation Accompanied by Symptomatic Cerebrospinal Fluid Hypovolemia: Comparison of Congenital Chiari Type-1 Malformation and Acquired Chiari Malformation Secondary to Cerebrospinal Fluid Hypovolemia: Case Report [J] . Ryusuke HATAE, Ryusuke KOHRI, Kazushi MAEDA, Neurologia medico-chirurgica. . 2014,第7期

机译：有症状性脑脊液血容量减少伴有Chiari 1型畸形的罕见病例：先天性Chiari 1型畸形与继发于脑脊液血容量不足的获得性Chiari畸形的比较：病例报告
4. Is curve direction correlated with the side of dominant displacement of cerebellar tonsil and syrinx deviation in thoracic scoliosis secondary to Chiari Malformation Type I and syringomyelia? [C] . Tao WU, Zezhang ZHU, Xu SUN, International Research Society of Spinal Deformities . 2012

机译：是曲线方向与小脑扁桃体的主导位移的一侧相关，胸腔肌肌肌肌肌瘤中学到Chiari畸形I型和射入肌瘤吗？
5. Magnetic resonance image-based hydrodynamic analysis of cerebrospinal fluid motion in Type I Chiari malformation. [D] . Shaffer, Nicholas M. 2014

机译：基于磁共振图像的脑脊液运动在I型Chiari畸形中的流体动力学分析。
6. Chiari malformation type I with cervicothoracic syringomyelia masquerading as bibrachial amyotrophy: a case report [O] . Jeffrey R Mora, Richard A Rison, Said R Beydoun 2015

机译：伪装为双臂性肌萎缩的颈胸椎型脊髓空洞症的Chiari畸形I型：一例报告
7. Chiari malformation type I with cervicothoracic syringomyelia masquerading as bibrachial amyotrophy: a case report [O] . 2015

机译：伪装为双臂性肌萎缩的颈胸椎型脊髓空洞症的Chiari畸形I型：一例报告

Chiari malformation type I with cervicothoracic syringomyelia masquerading as bibrachial amyotrophy: a case report

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