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视交叉海绵状畸形的清醒显微手术切除

Awake Microsurgical Resection for Optochiasmatic Cavernous Malformation.

作者信息

Alejandro Sebastián Aníbal, Serrato-Avila Juan Leonardo, Paganelli Samantha Lorena, Chang Mulato José Ernesto, Vela Rojas Evelyn Judith, Viera Neves Ana Paula, de Souza Coelho Daniela, Silva da Costa Marcos Devanir, Dória-Netto Hugo Leonardo, Campos Filho José Maria, Chaddad-Neto Feres

机构信息

Department of Neurosurgery, Universidade Federal de Sao Paulo, São Paulo-SP, Brazil.

Department of Neurosurgery, Universidade Federal de Sao Paulo, São Paulo-SP, Brazil; Hospital Beneficência Portuguesa de São Paulo, São Paulo-SP, Brazil.

出版信息

World Neurosurg. 2022 Jan;157:159. doi: 10.1016/j.wneu.2021.10.104. Epub 2021 Oct 21.

Abstract

Cavernous malformations (CM) affect approximately 0.5% of the population, with only a limited portion being located in the optic nerve and chiasma. The clinical presentation is determined by their locations. In the optochiasmatic CM, the acute visual disturbance is the most common presentation. Chronically, many show a progressive visual loss, chronic headache, and pituitary disturbances. The differential diagnosis includes optic glioma, arteriovenous malformations, aneurysm, craniopharyngioma, pituitary apoplexy, and inflammatory conditions. In Video 1, we present the case of a 39-year-old woman with a history of a hemorrhagic optochiasmatic cavernoma in 2016, who started using propranolol to reduce the lesion and symptoms of visual loss. Moreover, the first microsurgical resection of the cavernoma and evacuation of the hematoma were performed in the same year. Owing to evolvement from a partial to a total vision loss in the left eye and presentation of new symptoms in the right eye, the patient underwent microsurgical resection. The surgery was performed sequentially. An awake craniotomy was performed to monitor the chiasma and right optic nerve. The postoperative magnetic resonance imaging showed complete resection of the CM, and the patient fully recovered. The patient signed the institutional consent form, stating that he or she accepts the procedure and allows the use of his or her images and videos for any type of medical publications in conferences and/or scientific articles.

摘要

海绵状血管畸形(CM)影响约0.5%的人群,其中仅有一小部分位于视神经和视交叉。临床表现取决于其位置。在视交叉海绵状血管畸形中,急性视力障碍是最常见的表现。长期来看,许多患者表现为进行性视力丧失、慢性头痛和垂体功能障碍。鉴别诊断包括视神经胶质瘤、动静脉畸形、动脉瘤、颅咽管瘤、垂体卒中以及炎症性疾病。在视频1中,我们展示了一名39岁女性的病例,该患者在2016年有出血性视交叉海绵状血管瘤病史,开始使用普萘洛尔来缩小病灶并减轻视力丧失症状。此外,同年对海绵状血管瘤进行了首次显微手术切除并清除了血肿。由于左眼视力从部分丧失发展为完全丧失,且右眼出现新症状,患者接受了显微手术切除。手术分阶段进行。进行了清醒开颅手术以监测视交叉和右侧视神经。术后磁共振成像显示海绵状血管畸形完全切除,患者完全康复。患者签署了机构同意书,表明其接受该手术,并允许将其图像和视频用于会议中的任何类型医学出版物和/或科学文章。

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