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钩回部海绵状血管畸形的显微切除术:3D 手术视频。

Microsurgical Resection for Cavernous Malformation of the Uncus: 3D-Operative Video.

机构信息

Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, São Paulo, Brazil; Department of Neurosurgery, Hospital Beneficência Portuguesa de São Paulo, São Paulo, Brazil.

Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, São Paulo, Brazil.

出版信息

World Neurosurg. 2024 Jun;186:50. doi: 10.1016/j.wneu.2024.03.053. Epub 2024 Mar 20.

DOI:10.1016/j.wneu.2024.03.053
PMID:38514032
Abstract

Cavernous malformations (CMs) are rare and often oligosymptomatic vascular lesions. The main symptoms include seizure and focal neurologic deficits. Depending on the symptomatology, location, size, and risk factors for bleeding, like the presence of a developmental venous anomaly, CMs can be highly morbid. Thus surgical resection may be considered. Deep-seated and eloquent CMs, like those in the uncus, can be challenging. In Video 1, we present a 23-year-old male adult who developed focal seizures (i.e., oral automatisms) after an episode of sudden intense headache 1 year ago. His neurologic examination was unremarkable. The patient consented to the procedure and publication of his image. Nevertheless, his magnetic resonance images showed an uncal 2-cm Zabramski type I CM. We exposed the insula and its limen through a right pterional craniotomy and transsylvian corridor. During the video, we discuss the surgical nuances to access and resect this CM lesion en bloc while preserving important vascular structures and white matter tracts. Postoperative neuroimaging demonstrated total resection. In postoperative day 1, the patient had 1 episode of generalized seizure and evolved with contralateral hemiparesis. The patient had a good recovery and was discharged on postoperative day 21. At the 6-month follow-up, the patient had no new epileptic events and presented complete weakness improvement. Through this minimally invasive and well-known surgical corridor, we preserve the mesial and lateral portion of the temporal lobe, reducing the risk of lesions to the Meyer loop and limbic association area.

摘要

海绵状血管畸形(CM)是一种罕见的、常表现为寡症状的血管病变。主要症状包括癫痫发作和局灶性神经功能缺损。根据症状、位置、大小以及出血的危险因素,如是否存在发育性静脉异常,CM 可能会导致高度病态。因此,可能需要考虑手术切除。位于深部和重要功能区的 CM,如位于钩回的 CM,手术切除极具挑战性。在视频 1 中,我们介绍了一位 23 岁的男性成年人,他在 1 年前突发剧烈头痛后出现局灶性癫痫发作(即口腔自动症)。他的神经系统检查无明显异常。患者同意进行手术并同意发布其图像。然而,他的磁共振成像显示存在 2cm 大小的 Zabramski Ⅰ型钩回 CM。我们通过右侧翼点开颅和经侧裂入路暴露岛叶及其脑岛周皮质。在视频中,我们讨论了手术的细微之处,以整块切除该 CM 病变,同时保护重要的血管结构和白质束。术后神经影像学检查显示完全切除。术后第 1 天,患者发生 1 次全面性癫痫发作,伴对侧偏瘫。患者恢复良好,术后第 21 天出院。术后 6 个月随访时,患者未再出现新的癫痫发作,且完全性瘫痪得到改善。通过这种微创且广为人知的手术入路,我们保留了颞叶的内侧和外侧部分,降低了对 Meyer 环和边缘系统联系区的损伤风险。

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