Budke Marcelo, Pérez-Jiménez María Ángeles, Mena-Bernal José Hinojosa
Department of Pediatric Neurosurgery, Niño Jesús Hospital, Madrid, Spain.
Department of Pediatric Neurosurgery, Sant Joan de Déu Hospital, Barcelona, Spain.
Oper Neurosurg (Hagerstown). 2020 Aug 1;19(2):E159-E160. doi: 10.1093/ons/opaa055.
Hypothalamic hamartomas often cause refractory epilepsy, best controlled with surgery. A transcallosal interforniceal approach provides good outcomes although it has resulted in some complications including fornix lesions with transitory and permanent memory losses.1-2 Endoscopic disconnection is less invasive, avoids interhemispheric approach, callosotomy and fornix as well as propagation of epileptic discharges.3,4 Laser disconnection does not allow objective measurement of the vaporized tissue and can cause significant hypothalamic edema. We demonstrate a simple hypothalamic disconnection endoscopy technique using the VarioGuide frameless stereotactic system (Brainlab, Germany), bipolar coagulation electrode (Karl Storz, Germany), and 3-French Fogarty catheter (Edwards Lifesciences, USA). We present a 12-yr-old right-handed girl who developed normally until 4 yr old when gelastic seizures began. Antiepileptic drugs and gamma knife radiosurgery did not control the seizures. Magnetic resonance imaging showed a nodular 13 mm left hypothalamic mass protruding into the third ventricle. The patient consented to surgery. We used a rigid 30° 6-mm neuroendoscope (Aesculap, Germany) with VarioGuide to reach the ventricle. After visualizing the foramen of Monro, the bipolar coagulation electrode perforated holes along the hamartoma/hypothalamus interface. The Fogarty balloon catheter was inserted into each hole and gently inflated to connect the holes and disconnect the mass from the hypothalamus. The patient's postsurgical recovery was excellent, presenting intact short- and long-term memory without neurological deficit or endocrine complications. She continues seizure-free 2 yr after surgery. We have successfully used this technique in 4 more cases and, if results continue to be good, will consider it a useful tool for these infrequent malformations.
下丘脑错构瘤常导致难治性癫痫,手术是最佳的控制方法。经胼胝体穹窿间入路虽能取得较好疗效,但也会引发一些并发症,包括穹窿损伤以及短暂和永久性记忆丧失。1 - 2 内镜下离断术侵入性较小,避免了经半球间入路、胼胝体切开术和穹窿,以及癫痫放电的传播。3,4 激光离断术无法客观测量汽化组织,还可能导致明显的下丘脑水肿。我们展示了一种使用VarioGuide无框架立体定向系统(德国Brainlab公司)、双极电凝电极(德国Karl Storz公司)和3 - 法国Fogarty导管(美国Edwards Lifesciences公司)的简单下丘脑离断内镜技术。 我们报告一名12岁右利手女孩,她4岁前发育正常,之后出现痴笑发作。抗癫痫药物和伽玛刀放射外科治疗均未能控制癫痫发作。磁共振成像显示左侧下丘脑有一个13毫米的结节状肿块突入第三脑室。患者同意接受手术。 我们使用带有VarioGuide的刚性30°6毫米神经内镜(德国Aesculap公司)进入脑室。在观察到室间孔后,双极电凝电极沿错构瘤/下丘脑界面打孔。将Fogarty球囊导管插入每个孔中并轻轻充气,以连接这些孔并将肿块与下丘脑离断。 患者术后恢复良好,短期和长期记忆完整,无神经功能缺损或内分泌并发症。术后2年她一直无癫痫发作。我们已在另外4例患者中成功应用了该技术,如果结果持续良好,将认为它是治疗这些罕见畸形的一种有用工具。