Higashi S, Higashi Y, Kuroda S, Kohira I, Kanzaki A
Division of Neurology, Himeji Central Hospital.
Rinsho Shinkeigaku. 1992 Apr;32(4):405-11.
A case of subacute sclerosing panencephalitis (SSPE) was reported. The patient was a 16-year-old boy and he initially developed visual disturbance. His neurologic symptoms were myoclonus, dementia, and visual disturbance which was rare as an initial symptom in SSPE. Fundoscopy revealed bilateral pole chorioretinitis and macular degeneration. Serial MRI study demonstrated the lesions in the brain and right eye ball. The distribution varied as time went on. T2-weighted MR images showed the lesions more clearly than T1-weighted MR images. In this case dementia was marked but the lesions in the cerebrum on the MR images were considerably smaller than expected. Although MR image is useful to show the lesions, the discrepancy between clinical signs and MR images may be present in the early stage in SSPE.
报告了1例亚急性硬化性全脑炎(SSPE)。患者为一名16岁男孩,最初出现视觉障碍。他的神经症状为肌阵挛、痴呆和视觉障碍,而视觉障碍作为SSPE的初始症状较为罕见。眼底检查显示双侧极部脉络膜视网膜炎和黄斑变性。系列MRI研究显示脑部和右眼球有病变。病变分布随时间变化。T2加权MR图像比T1加权MR图像更清晰地显示病变。该病例中痴呆明显,但MR图像上大脑中的病变比预期小得多。虽然MR图像有助于显示病变,但在SSPE早期可能存在临床体征与MR图像之间的差异。