Ohkawa S, Mori E, Ohsumi Y, Tabuchi M, Yamadori A
Neurology Service, Hyogo Brain and Heart Center, Himeji.
Rinsho Shinkeigaku. 1992 Nov;32(11):1277-80.
A 31-year-old woman with a history of suspected optic neuritis was admitted with weakness of right-sided extremities and confusion. On admission general physical examination revealed no abnormality. Neurological examination revealed central facial palsy, mild hemiparesis and hemisensory deficit on the right side. Cerebrospinal fluid analysis showed monocytosis of 29 cells, protein of 82 mg/dl, glucose of 62 mg/dl and myelin basic protein of 6.8 ng/ml. No oligoclonal bands were seen. X-ray computed tomographic (CT) scans showed multiple homogeneous contrast-enhancing lesions in the white matter of bilateral parietal lobes without distinct edema or mass effect. Follow-up CT scans showed ring-enhanced lesions. Magnetic resonance image (MRI) showed multiple Gadolinium-enhanced lesions. Additionally, 123I-IMP SPECT [Gamma view-SPCT 2000 H-20 (Hitachi Co.)] was performed at 30 minutes and 5 hours after intravenous administration of IMP (3 mCi). It showed high IMP uptake corresponding to the CT and MRI lesions. Cerebral angiography was considered to be normal. Other laboratory findings were within normal limits. A biopsy was performed. Histological examination showed spongiosis, gliosis and perivascular cuffing. The histological diagnosis was acute demyelinating disease. After therapy with methylprednisolone, she improved gradually. Enhanced lesions in CT and MRI may correspond to active demyelination at acute MS. High uptake of SPECT may also appear in acute stage, although it has not been reported. We should perform neuro-imaging studies including SPECT on acute MS.
一名有视神经炎疑似病史的31岁女性因右侧肢体无力和意识模糊入院。入院时全身体格检查未发现异常。神经系统检查发现中枢性面瘫、轻度偏瘫和右侧半身感觉障碍。脑脊液分析显示单核细胞增多,有29个细胞,蛋白82mg/dl,葡萄糖62mg/dl,髓鞘碱性蛋白6.8ng/ml。未发现寡克隆带。X线计算机断层扫描(CT)显示双侧顶叶白质有多个均匀强化的病灶,无明显水肿或占位效应。随访CT扫描显示环形强化病灶。磁共振成像(MRI)显示多个钆强化病灶。此外,静脉注射IMP(3mCi)后30分钟和5小时进行了123I-IMP单光子发射计算机断层扫描(SPECT)[Gamma view-SPCT 2000 H-20(日立公司)]。结果显示与CT和MRI病灶相对应的IMP摄取增高。脑血管造影被认为正常。其他实验室检查结果均在正常范围内。进行了活检。组织学检查显示有海绵状变性、胶质细胞增生和血管周围套袖现象。组织学诊断为急性脱髓鞘疾病。经甲基泼尼松龙治疗后,她逐渐好转。CT和MRI中的强化病灶可能与急性多发性硬化症(MS)的活动性脱髓鞘相对应。SPECT的高摄取在急性期也可能出现,尽管尚未见报道。对于急性MS,我们应进行包括SPECT在内的神经影像学检查。