Eagle syndrome with repeated transient disturbances of consciousness diagnosed using digital subtraction angiography with head rotation: illustrative case.

Hiroki Kobayashi, Yoshinori Kotani, Mamoru Ogiso, Yusuke Egashira, Shinji Noda
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Abstract

Background: Eagle syndrome with repeated transient disturbances of consciousness is uncommon, with only a few reported cases. Here, the authors report a rare case of Eagle syndrome with repeated transient disturbances of consciousness in a specific head position, diagnosed using digital subtraction angiography (DSA) with head rotation.

Observations: A 74-year-old man experienced several episodes of transient disturbance of consciousness. When he stared downward toward the left, he experienced transient tremors in the right upper and lower limbs and a transient loss of consciousness. Magnetic resonance imaging failed to identify the cause. DSA performed with external head rotation and leftward flexion revealed a delay of blood flow distal to the cervical portion of the left internal carotid artery caused by compression from the left styloid process. A superficial temporal artery-middle cerebral artery (STA-MCA) bypass was required in the right cerebral hemisphere. The styloid process was removed first, as the head needed leftward rotation during surgery. Transient disturbance of consciousness did not recur after surgery. Four months later, a right STA-MCA bypass was performed.

Lessons: This case highlights Eagle syndrome as a potential cause of repeated transient disturbances of consciousness. DSA with head rotation proved useful for the diagnosis. https://thejns.org/doi/10.3171/CASE24744.

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利用旋转头部的数字减影血管造影术诊断出反复出现短暂意识障碍的伊格尔综合征:示例病例。
背景:伴有反复短暂性意识障碍的鹰综合征并不常见,仅有少数病例报道。在这里,作者报告了一例罕见的鹰综合征,在特定的头部位置反复出现短暂的意识障碍,使用头部旋转的数字减影血管造影(DSA)诊断。观察:一位74岁的男性经历了几次短暂的意识障碍。当他向下看向左边时,他的右上肢和下肢经历了短暂的震颤,并短暂地失去了意识。磁共振成像无法确定病因。头部外旋和左屈时的DSA显示,由于左侧茎突压迫导致左颈内动脉颈段远端血流延迟。右脑半球需要行颞浅动脉-大脑中动脉(STA-MCA)旁路手术。茎突首先被切除,因为在手术中头部需要向左旋转。术后未出现短暂性意识障碍。4个月后,行右STA-MCA旁路手术。经验教训:本病例强调Eagle综合征是反复短暂性意识障碍的潜在原因。头部旋转的DSA对诊断有用。https://thejns.org/doi/10.3171/CASE24744。
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