Schulman J A, Shults W T, Jones J M
Am J Ophthalmol. 1979 Jan;87(1):87-90. doi: 10.1016/0002-9394(79)90197-1.
A 5-year-old boy with monocular vertical nystagmus, initially believed to have spasmus nutans, subsequently developed optic atrophy and visual loss. Neuroradiologic investigation indicated probable chiasmal glioma. The case of this patient re-emphasizes the necessity of careful clinical and radiologic assessment before assuming acquired monocular nystagmus to be a benign and self-limited disorder.
一名患有单眼垂直性眼球震颤的5岁男孩，最初被认为患有痉挛性斜颈，随后出现视神经萎缩和视力丧失。神经放射学检查表明可能患有视交叉胶质瘤。该患者的病例再次强调了在将后天性单眼眼球震颤假定为良性自限性疾病之前，进行仔细的临床和放射学评估的必要性。
