动静脉畸形放射手术后延迟囊肿形成:病例报告与评论。

Surgical neurology international Pub Date : 2024-10-11 eCollection Date: 2024-01-01 DOI:10.25259/SNI_391_2024
João Meira Gonçalves, António Vilarinho, Vasco Carvalho, Patrícia Polónia, Pedro Alberto Silva
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摘要

背景:立体定向放射外科(SRS)是治疗脑动静脉畸形(AVM)的有效方法,尽管人们对其潜在的延迟并发症仍有更多的了解:一名 49 岁的男子患有左侧中央核心动静脉畸形,深静脉引流至大脑内静脉(斯佩茨勒-马丁 4 级),尽管他在两个不同的时间点接受了伽马刀放射外科治疗,并确认几乎完全消失,但在大约 10 年的随访间隔内,他还是多次出现脑出血。第一次放射手术治疗后约 10 年,他出现了严重的运动性失语、3 级右偏瘫、进行性意识模糊和记忆障碍。脑成像显示 AVM 周围有囊变性。医生尝试了囊肿切开术和腹腔分流术。这些治疗方法暂时有效,但囊肿进行性增大复发,临床症状恶化。因此,医生建议患者通过大脑半球间经胼胝体入路手术切除肿块和囊肿。术后磁共振成像显示病灶完全切除,术后恢复顺利。在 6 个月的随访中,患者的言语、力量和灵活性均有明显改善,并能自主行走:结论:动静脉畸形的囊性变性是 SRS 术后可能出现的长期并发症。结论:动静脉畸形囊性变性是 SRS 术后可能出现的长期并发症,对此类患者的长期随访和数据收集仍然至关重要,即使有证据表明动静脉畸形已完全消失。
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Delayed cyst formation after radiosurgery for arteriovenous malformation: A case report and critical review.

Background: Stereotactic radiosurgery (SRS) is a validated treatment option for cerebral arteriovenous malformations (AVMs), even if a greater knowledge of its potential delayed complications is still being acquired.

Case description: A 49-year-old man suffered multiple episodes of cerebral hemorrhage in an approximate 10-year follow-up interval in the context of a left central core AVM with deep venous drainage into the internal cerebral veins (Spetzler Martin Grade 4) despite being treated with gamma knife radiosurgery at two separate timepoints, and with an almost complete obliteration confirmed. Approximately 10 years after the first radiosurgery treatment, he developed severe motor aphasia, Grade 3 right hemiparesis, progressive confusion, and memory deficits. Cerebral imaging revealed cystic degeneration in the AVM's periphery. Cyst fenestration and cystoperitoneal shunt were attempted. The treatments were temporarily effective, but a progressive cyst enlargement recurred with clinical deterioration. The patient was therefore proposed for surgical mass and cyst excision through an interhemispheric transcallosal approach. The postoperative magnetic resonance imaging showed complete removal of the lesion, and an uneventful post-operative course ensued. At the 6-month follow-up, our patient experienced a noticeable improvement in his speech, power, dexterity and was able to walk autonomously.

Conclusion: Cystic degeneration of AVMs is a possible long-term complication after SRS. Long-term follow-up and data on such patients remain crucial, even with evidence of complete nidal obliteration.

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