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[多发性硬化症患者脊髓空洞形成的系列磁共振成像]

[Serial magnetic resonance imaging of spinal syrinx formation in a case of multiple sclerosis].

作者信息

Ando T, Kameyama T, Kawai K, Fukatsu H, Takahashi A

机构信息

Department of Neurology, Nagoya University School of Medicine.

出版信息

Rinsho Shinkeigaku. 1992 Nov;32(11):1288-93.

PMID:1301334
Abstract

A 27-year-old woman had a subacute onset of back pain, dysesthesia and weakness of both arms. Neurological examination revealed bilateral pyramidal signs, paresthesia of both hands and arms, and hypalgesia below T-4. CSF showed no abnormal findings. T2-weighted MR images revealed linear high signal within the cervical and upper thoracic cord, but no syrinx. The signs and symptoms resolved substantially within three months, with the exception of paroxysmal itching localized to the right forearm. At age 30, she experienced an acute onset of back pain, and dysesthesia of both feet. She developed weakness of both legs and urinary retention two days after the onset. Neurological examination showed bilateral pyramidal signs in the lower extremities, hypalgesia below T-4, hypopallesthesia on both legs, but no abnormalities in the upper extremities. CSF contained 8 white cells/mm3, protein 17 mg/dl and glucose 44 mg/dl. Oligoclonal bands were not detected. T1-weighted, proton density, and T2-weighted MR images revealed a syrinx formation within the spinal cord, extending from the level of T-2 to T-5. There was no evidence of spinal tumor. MRI of the brain revealed multiple areas of high signal intensity on T2-weighted image, consistent with multiple sclerosis. The signs and symptoms resolved substantially within two months. The syrinx within the thoracic cord reduced in size after two months and disappeared after three months. Two months after the second episode of myelopathy, she experienced right optic neuritis, resolving substantially within three weeks. This case was diagnosed as definite multiple sclerosis based on the clinical and radiological findings.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一名27岁女性出现亚急性背痛、感觉异常和双臂无力。神经系统检查发现双侧锥体束征、双手和双臂感觉异常,以及T-4以下痛觉减退。脑脊液检查未见异常。T2加权磁共振成像显示颈髓和上胸髓内有条状高信号,但无空洞形成。除右前臂阵发性瘙痒外,体征和症状在三个月内基本缓解。30岁时,她突发背痛和双足感觉异常。发病两天后出现双腿无力和尿潴留。神经系统检查显示双下肢双侧锥体束征、T-4以下痛觉减退、双下肢触觉减退,但上肢无异常。脑脊液白细胞计数为8个/mm³,蛋白17mg/dl,葡萄糖44mg/dl。未检测到寡克隆带。T1加权、质子密度加权和T2加权磁共振成像显示脊髓内有空洞形成,从T-2水平延伸至T-5。无脊髓肿瘤证据。脑部磁共振成像显示T2加权像上有多个高信号区,符合多发性硬化表现。体征和症状在两个月内基本缓解。胸段脊髓空洞在两个月后缩小,三个月后消失。脊髓病第二次发作两个月后,她出现右视神经炎,三周内基本缓解。根据临床和影像学表现,该病例被诊断为明确的多发性硬化。(摘要截短至250字)

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