Prolonged visual aura, late-onset migraine-like headaches, and seizures suggest an occipital arteriovenous malformation.

IF 1.1 Q4 PRIMARY HEALTH CARE
Josef Finsterer, Sounira Mehri
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引用次数: 0

Abstract

To report a patient with occipital arteriovenous malformation (AVM), manifested by prolonged visual aura and migraine-like headache as well as rare tonic-clonic seizures. The patient is a 55-year-old woman with a left occipital, unruptured AVM that first manifested with attacks of prolonged visual aura, followed by a migraine-like headache at the age of 32. The frequency of these attacks steadily increased over the years and at the age of 45 she experienced her first tonic-clonic seizure. The workup revealed a left occipital, unruptured AVM. She received levetiracetam (1000 mg/d), which she discontinued at the age of 53. At the age of 54 years, she suffered a second tonic-clonic seizure, but the patient continued to refuse to undergo embolization, resection, or stereotactic radiosurgery. This case demonstrates that an occipital, unruptured AVM can go undetected for years and present with late-onset, migraine-like headaches with prolonged visual aura and rare generalized seizures. Patients with late-onset, migraine-like headaches with prolonged visual aura require immediate brain imaging.

视觉先兆延长,晚发型偏头痛样头痛和癫痫发作提示枕动静脉畸形。
报告一例枕动静脉畸形(AVM)患者,表现为长时间的视觉先兆和偏头痛样头痛,以及罕见的强直阵挛性癫痫发作。患者是一名55岁女性,患有左枕部未破裂的AVM,首次表现为长时间的视觉先兆发作,随后在32岁时出现偏头痛样头痛。这些发作的频率逐年稳步增加,在45岁时,她经历了第一次强直阵挛发作。检查发现左枕骨未破裂的动静脉畸形。患者接受左乙拉西坦(1000mg /d)治疗,于53岁停用。在54岁时,她遭受了第二次强直阵挛发作,但患者继续拒绝接受栓塞,切除或立体定向放射手术。本病例表明枕部未破裂的动静脉畸形可多年未被发现,表现为晚发性偏头痛样头痛,伴有长时间的视觉先兆和罕见的全身性癫痫发作。迟发性偏头痛样头痛且视觉先兆延长的患者需要立即进行脑成像。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
7.10%
发文量
884
审稿时长
40 weeks
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