Sawhney I M, Chopra J S, Bansal S K, Gupta A K
Clin Neurol Neurosurg. 1986;88(3):213-5. doi: 10.1016/s0303-8467(86)80032-4.
Two cases of Eales' disease with myelopathy are reported. The first case evinced spastic paraplegia and minimal bladder dysfunction. The unusual features were that the neurologic deficit progressed over 2 years and sensations were normal. Cerebrospinal fluid (CSF) proteins were raised. Visual evoked responses (VER) and brain stem evoked responses (BSER) were normal. The second case evinced brain stem involvement in addition to dorsal myelopathy. CSF examination showed lymphocytic pleocytosis.
报告了两例伴有脊髓病的伊尔斯病。第一例表现为痉挛性截瘫和轻微膀胱功能障碍。其不寻常之处在于神经功能缺损在2年中逐渐进展且感觉正常。脑脊液（CSF）蛋白升高。视觉诱发电位（VER）和脑干诱发电位（BSER）正常。第二例除了脊髓后索病变外还表现出脑干受累。脑脊液检查显示淋巴细胞增多。
