Albertus Daniel L, Pipitone Baldassare, Srinivasan Ashok, Trobe Jonathan D
Kellogg Eye Center, Department of Ophthalmology and Visual Sciences, University of Michigan, United States.
Department of Radiology (Neuroradiology), University of Michigan, United States.
Am J Ophthalmol Case Rep. 2017 May 18;7:50-54. doi: 10.1016/j.ajoc.2017.05.003. eCollection 2017 Sep.
To present an example of how close clinical monitoring of a patient with acute Horner syndrome from carotid artery dissection may be critical in reversing neurologic dysfunction.
A patient whose initial neuro-ophthalmic manifestation was Horner syndrome, but who evolved over 14 days to display transient monocular vision loss, ipsilateral ocular ischemic syndrome, and episodic contralateral hemiparesis. Digital subtraction angiography demonstrated progressive ipsilateral carotid occlusion with lack of collateral flow. The patient underwent stenting with rapid reversal of transient monocular visual loss and hemiparesis. Follow-up examination several months later confirmed complete resolution of all clinical abnormalities.
This case displayed protracted evolution of ischemic manifestations following carotid artery dissection and their prompt reversal with stenting. This case emphasizes the value of close clinical attention to a patient with acute Horner syndrome because manifestations may appear more than 10 days after event onset that impel intervention for the dissection.
举例说明对因颈动脉夹层导致急性霍纳综合征患者进行密切临床监测对于逆转神经功能障碍可能至关重要。
一名患者最初的神经眼科表现为霍纳综合征,但在14天内病情进展,出现短暂性单眼视力丧失、同侧眼部缺血综合征和发作性对侧偏瘫。数字减影血管造影显示同侧颈动脉逐渐闭塞且无侧支血流。该患者接受了支架置入术,短暂性单眼视力丧失和偏瘫迅速逆转。数月后的随访检查证实所有临床异常均已完全消失。
该病例显示了颈动脉夹层后缺血表现的迁延演变以及支架置入术使其迅速逆转。该病例强调了对急性霍纳综合征患者进行密切临床关注的价值,因为在事件发生10天以上可能会出现促使对夹层进行干预的表现。