Abstract
Purpose
To describe two cases of stereotyped, intermittent, neurologically isolated, unilateral mydriasis in patients with a history of acquired internal carotid artery (ICA) occlusive disease on the ipsilateral side.
Patients
Two patients with intermittent mydriasis.
Methods
Case Series.
Results
Case one: A 78-year-old man experienced 10 episodes of intermittent, unilateral, and painless mydriasis in the left eye and had 100% occlusion of the left ICA artery due to atherosclerotic disease. Case two: A 26-year-old woman with history of migraine developed new painless, intermittent episodes of unilateral mydriasis after sustaining chest trauma and was diagnosed with subsequent dissection and 65% occlusion of the ipsilateral ICA. Neither patient developed permanent anisocoria.
Conclusion
Benign episodic unilateral mydriasis (BEUM) typically presents in young women with a history of migraine. To our knowledge, these are the first cases of episodic, unilateral, neurologically isolated mydriasis associated with occlusive disease of the ICA in the English language ophthalmic literature. We hypothesize that transient dysfunction of the autonomic nervous system related to the ICA disease may account for the intermittent mydriatic episodes in these patients and we recommend consideration for imaging of the ICA in patients with atypical features for BEUM (for example, old age or males, non-isolated mydriasis, or recent trauma).
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References
Jacobson DM . Benign episodic unilateral mydriasis. Ophthalmology 1995; 102 (11): 1623–1627.
Ibrahim M, Branson HM, Buncic JR, Shroff MM . A case of Horner syndrome with intermittent mydriasis in a patient with hypoplasia of the internal carotid artery. AJNR Am J Neuroradiol 2006; 27 (6): 1318–1320.
Orssaud C, Roche O, Renard G, Dufier JL . Carotid artery dissection revealed by an oculosympathetic spasm. J Emerg Med 2010; 39 (5): 586–588.
Kline LB, McCluer SM, Bonikowski FP . Oculosympathetic spasm with cervical spinal cord injury. Arch Neurol 1984; 41 (1): 61–64.
Sharma GK, Deshmukh VR, Albuquerque FC, Wolf TR, McDougall CG . Resolution of mydriatic pupil after angioplasty and stenting of cervical internal carotid artery dissection: case report. Neurosurgery 2009; 64 (3): E562–E563.
Inzelberg R, Nisipeanu P, Blumen SC, Kovach I, Groisman GM, Carasso RL . Transient unilateral mydriasis as the presenting sign of aortic and carotid dissection. Neurology 2000; 55 (12): 1934–1935.
Koennecke H, Seyfert S . Mydriatic pupil as the presenting sign of common carotid artery dissection. Stroke 1998; 29 (12): 2653–2655.
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Chamberlain, P., Sadaka, A., Berry, S. et al. Intermittent mydriasis associated with carotid vascular occlusion. Eye 32, 457–459 (2018). https://doi.org/10.1038/eye.2017.127
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DOI: https://doi.org/10.1038/eye.2017.127


