Bilateral inferior colliculus infarction after embolization of a cerebellar arteriovenous malformation: illustrative case.

Cafer Ikbal Gulsever, Alperen Poyraz, Duygu Dolen, Tugrul Cem Unal, Ilyas Dolas, Mehmet Barburoglu, Nebiye Serra Sencer, Yavuz Aras
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Abstract

Background: Bilateral inferior colliculus (IC) infarction is a rare condition that can lead to severe auditory deficits. Cerebellar arteriovenous malformations (AVMs) treated with endovascular embolization pose a risk for ischemic complications affecting the brainstem.

Observations: A 54-year-old male presented with intermittent headaches and imbalance, and, following a fall, a subarachnoid hemorrhage and cerebellar AVM were identified. After endovascular embolization, the patient developed bilateral moderate hearing loss, and MRI revealed acute ischemia in both ICs. Despite treatment with intravenous hydration and prednisolone, the patient's hearing loss progressed to total sensorineural hearing loss. Audiometry and auditory brainstem response testing showed reduced amplitudes, although some responses were still present. At 4 months, further amplitude reduction occurred, but the patient began using written communication and lipreading.

Lessons: Bilateral IC infarction is an uncommon but significant complication following cerebellar AVM embolization. Early recognition and supportive care, including rehabilitation, are essential for patient adaptation. To minimize the risk of brainstem infarction, embolization should be performed as close to the AVM nidus as possible, avoiding unnecessary involvement of brainstem feeders. https://thejns.org/doi/10.3171/CASE24712.

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小脑动静脉畸形栓塞后双侧下丘梗死:说明性病例。
背景:双侧下丘(IC)梗死是一种罕见的疾病,可导致严重的听觉障碍。小脑动静脉畸形(AVMs)治疗血管内栓塞有影响脑干的缺血性并发症的风险。观察结果:一名54岁男性患者表现为间歇性头痛和身体失衡,并在跌倒后发现蛛网膜下腔出血和小脑AVM。血管内栓塞后,患者出现双侧中度听力损失,MRI显示双侧ici急性缺血。尽管给予静脉补水和泼尼松龙治疗,患者的听力损失仍发展为全感音神经性听力损失。听力测量和听觉脑干反应测试显示振幅降低,尽管一些反应仍然存在。4个月时,振幅进一步下降,但患者开始使用书面交流和唇读。结论:双侧IC梗死是小脑AVM栓塞后罕见但重要的并发症。早期识别和支持性护理,包括康复,对患者适应至关重要。为了降低脑干梗死的风险,栓塞术应尽可能靠近动静脉窦,避免不必要的脑干输注器介入。https://thejns.org/doi/10.3171/CASE24712。
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