Microvascular decompression for developmental venous anomaly causing hemifacial spasm: illustrative case

被引:1
作者
Tugend, Margaret [1 ]
Sekula Jr, Raymond F. [1 ]
机构
[1] Columbia Univ, New York Presbyterian Hosp, Dept Neurol Surg, New York, NY USA
来源
JOURNAL OF NEUROSURGERY-CASE LESSONS | 2024年 / 7卷 / 01期
关键词
developmental venous anomaly; case report; hemifacial spasm; microvascular decompression; pontine; ANGIOMA;
D O I
10.3171/CASE23479
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND Developmental venous anomaly (DVA) is a rare cause of hemifacial spasm (HFS). The treatment of HFS caused by a DVA varies in the literature and includes medication management, botulinum toxin injections, and microvascular decompression (MVD). OBSERVATIONS A 64-year-old woman presented with right-sided HFS. Preoperative magnetic resonance imaging showed a DVA in the right inferior pons, with an enlarged segment compressing the facial nerve at its root detachment point prior to drainage into the superior petrosal sinus. MVD was performed, and the facial nerve was decompressed without sacrifice of the vein. Immediately following the procedure, the patient had significantly reduced spasms. The patient became spasm-free 3 months after MVD and maintained spasm freedom for 3 months. Six months after MVD, the patient had a partial return of spasms. At 8 months, the patient continued to have reduced and intermittent spasms in the right orbicularis oculi muscle. LESSONS MVD for HFS caused by a DVA is a safe procedure and can be effective at reducing spasm frequency and severity.
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页数:4
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