Abstract
Background: Oculomotor nerve paresis may have relatively benign but also life-threatening causes. Distinguishing between these is of great clinical importance. Objective: To reveal a potential pitfall of the clinical evaluation of oculomotor nerve paresis. Patient: Single case observation. Results: A 56-year-old man had fluctuating diplopia and fatigable ptosis, promptly relieved by intravenous edrophonium, leading to the diagnosis of ocular myasthenia gravis. His pupillary function was intact. A few days after the initial diagnosis, he suffered a subarachnoid hemorrhage secondary to the rupture of a basilar artery aneurysm. His ocular symptoms were related to aneurysmal oculomotor nerve compression. Conclusion: Patients with oculomotor nerve dysfunction need more detailed evaluation because the underlying cause cannot be safely determined on a clinical basis.
| Original language | English |
|---|---|
| Pages (from-to) | 1448-1450 |
| Number of pages | 3 |
| Journal | Archives of Neurology |
| Volume | 61 |
| Issue number | 9 |
| DOIs | |
| State | Published - Sep 2004 |
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