特发性新生动静脉畸形:一种罕见的后天性颅内病变。

Tritan Plute, Prateek Agarwal, Aneek Patel, Arka N Mallela, L Dade Lunsford, Hussam Abou-Al-Shaar
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摘要

成人脑动静脉畸形(AVM)的重新发展是一种极其罕见的事件,这促使理论认为需要“第二次打击”来诱导AVM的形成。作者记录了在脑磁共振成像(MRI)未发现异常后15年成人枕部AVM的发展。一名31岁男性,有静脉畸形家族史,14年偏头痛病史,伴有视觉先兆和癫痫发作。由于17岁时首次发作和偏头痛,患者接受了高分辨率MRI检查,未发现颅内病变。14年后,症状逐渐恶化,他再次接受MRI检查,发现新的左枕部Spetzler-Martin 3级AVM。患者接受抗惊厥药物治疗,并因AVM接受伽玛刀放射治疗。本病例提示癫痫发作或持续性偏头痛患者应定期重复神经影像学检查,以排除血管病变,尽管最初MRI呈阴性。
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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Idiopathic De Novo Arteriovenous Malformation: A Rare Acquired Intracranial Lesion.

The de novo development of cerebral arteriovenous malformations (AVMs) in adults is an exceedingly rare event that has prompted the theory that a "second hit" is required to induce AVM formation. The authors document development of an occipital AVM in an adult a decade and a half after a brain magnetic resonance imaging (MRI) disclosed no abnormality. A 31-year-old male with a family history of AVMs and a 14-year history of migraines with visual auras and seizures presented to our service. Because of the onset of a first seizure and migraine headaches at age 17, the patient underwent high-resolution MRI that showed no intracranial lesion. After 14 years of progressively worsening symptoms, he underwent a repeat MRI that demonstrated a new de novo Spetzler-Martin grade 3 left occipital AVM. The patient received anticonvulsants and underwent Gamma Knife radiosurgery for his AVM. This case suggests that patients with seizures or persistent migraine headaches should have periodic repeat neuroimaging to exclude the development of a vascular cause despite an initial negative MRI.

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