Curless R G, Schatz N J, Bowen B C, Rodriguez Z, Ruiz A
Department of Neurology, Bascom Palmer Eye Institute, University of Miami School of Medicine, Florida, USA.
Pediatr Neurol. 1996 Oct;15(3):258-60. doi: 10.1016/s0887-8994(96)00172-5.
A 15-year-old boy had onset of unilateral facial weakness. A few days later, he experienced mild vertigo, double vision, and headache. Examination confirmed a peripheral right seventh nerve weakness in addition to an internuclear ophthalmoplegia. The neurologic features suggested a pontine glioma. A T2-weighted MRI scan revealed demyelinating lesions in the pons and in several areas of the cerebrum, including the periventricular region. Subsequent history revealed that he had been diagnosed with Lyme arthritis 7 years earlier while living in Connecticut. The radiographic studies favored a diagnosis of multiple sclerosis. However, studies of blood and cerebrospinal fluid established a diagnosis of Lyme neuroborreliosis.
一名15岁男孩出现单侧面部无力。几天后,他出现轻度眩晕、复视和头痛。检查证实除核间性眼肌麻痹外,右侧周围性面神经麻痹。神经系统特征提示为桥脑胶质瘤。T2加权磁共振成像扫描显示脑桥和大脑几个区域有脱髓鞘病变,包括脑室周围区域。随后的病史显示,他7年前在康涅狄格州生活时被诊断为莱姆关节炎。影像学检查结果倾向于多发性硬化症的诊断。然而,血液和脑脊液检查确诊为莱姆神经疏螺旋体病。