Hospital Madre Teresa, Belo Horizonte, Belo Horizonte, Minas Gerais, Brazil.
Hospital Municipal Miguel Couto, Rio de Janeiro, Brazil.
World Neurosurg. 2021 Dec;156:59. doi: 10.1016/j.wneu.2021.09.043. Epub 2021 Sep 21.
Cavernous malformations of the third ventricle are rare, deep-seated lesions that pose a formidable surgical challenge due to the rich, surrounding anatomy. Despite the potential morbidity of surgical treatment, the possibility of catastrophic, spontaneous hemorrhage in this location is even more feared and aggressive treatment is warranted, especially if the patient had suffered previous hemorrhages and is currently symptomatic. We demonstrate this approach (Video 1) on a 16-year-old boy who presented with right-sided hemiparesis (power grade 4), intense headaches, difficulties with learning and concentration, and memory loss, mainly affecting short-term memory. The patient had a previous unsuccessful excision at another center 3 months after initial hemorrhage. The absence of hydrocephalus and medial thalamic location favored a modified transcallosal transchoroidal (or subchoroidal) approach. Due to the anatomy of the lesion, no other microsurgical approaches were considered. The surgery at our center (second attempt) was performed 5 months after initial hemorrhage. The head was placed in neutral position, with a slight elevation of the vertex and the midline in a vertical position. A callosotomy had already been performed during the patient's first excision attempt at another center. Although dissection through the tela choroidea is commonly performed medially to the choroidal fissure when one wants to enter the third ventricle, we chose to carefully dissect through this structure laterally, because this thalamic lesion extended almost into the ependymal surface of the third ventricle. This way, the choroidal plexus became a protective cushion for the fornix. On entering the third ventricle, a mulberry-like lesion was readily identified and the cavernoma was located. The central contents of the cavernoma were dissected initially, causing relative deflation of the lesion and more maneuverability to dissect it away from the surrounding structures. Neuromonitoring was used to avoid brainstem injury. Postoperative magnetic resonance imaging showed complete resection with no signs of hemorrhage or ischemia. The patient was discharged on postoperative day 5 with no new neurologic deficits. The patient was also able to return to school after 1 month and showed complete recovery. Unfortunately, neuropsychologic evaluation was unavailable to understand his improvement better. Microsurgical dissection images in this video are a courtesy of the Rhoton Collection, American Association of Neurological Surgeons (AANS)/Neurosurgical Research and Education Foundation (NREF).
第三脑室海绵状畸形较为罕见,且病变位置较深,由于周围解剖结构丰富,给手术带来了巨大的挑战。尽管手术治疗可能带来一定的发病率,但在这个位置发生灾难性、自发性出血的可能性更令人担忧,因此需要进行积极的治疗,尤其是患者之前已经发生过出血,并且目前存在症状。我们通过一个 16 岁男孩的病例来演示这种方法(视频 1)。该男孩出现右侧偏瘫(肌力 4 级)、剧烈头痛、学习和注意力困难以及记忆力减退,主要影响短期记忆。该患者曾在另一家中心于初次出血后 3 个月行初次手术切除,但未成功。无脑积水和丘脑内侧位置有利于采用改良经胼胝体-经脉络膜(或脉络膜下)入路。由于病变的解剖结构,不考虑其他显微外科入路。该患者在初次出血后 5 个月于我们中心(第二次尝试)行手术治疗。头部置于中立位,顶点轻度抬高,中线垂直。在另一家中心的初次手术切除尝试中,已经进行了胼胝体切开术。虽然当想要进入第三脑室时,通常在脉络膜裂的内侧进行通过软脑膜的分离,但我们选择小心地从外侧分离这个结构,因为这个丘脑病变几乎延伸到第三脑室的室管膜表面。这样,脉络丛就成为穹窿的保护垫。进入第三脑室后,很容易识别出桑葚状病变,并定位海绵状畸形。首先解剖中央内容物,使病变相对瘪陷,更便于将其从周围结构中分离。使用神经监测避免脑干损伤。术后磁共振成像显示完全切除,无出血或缺血迹象。患者术后第 5 天出院,无新的神经功能缺损。患者在 1 个月后也能返校,并完全康复。不幸的是,无法获得神经心理学评估来更好地了解他的改善情况。本视频中的显微外科分离图像由美国神经外科医师协会(AANS)/神经外科研究与教育基金会(NREF)的 Rhoton 收藏提供。