Wang Min, Zhou Yuanfeng, Zhang Yi, Shi Wei, Zhou Shuizhen, Wang Yi, Li Hao, Zhao Rui
Department of Neurosurgery, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Department of Neurology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Front Neurol. 2020 Sep 2;11:965. doi: 10.3389/fneur.2020.00965. eCollection 2020.
Giant hypothalamic hamartomas (HHs) are extremely rare lesions, for which the treatment is challenging. While minimally invasive treatments such as radiofrequency thermal coagulation and laser ablation have improved seizure outcomes, multiple operations are often required. This study investigated the value of one-stage stereo-array radiofrequency thermocoagulation based on stereotactic electroencephalography (SEEG) for pediatric giant HHs. We analyzed the clinical data of six patients with giant HHs (masses with a maximum diameter >30 mm) who underwent stereotactic electrode implantation between November 2017 and April 2019. After a multidisciplinary discussion, we designed a high-density focal stereo-array electrode implantation strategy. SEEG-guided bipolar coagulations were performed between two contiguous contacts of the same electrode, or between two adjacent contacts of different electrodes. Among the six patients, three were male and three were female, with an average age of 5.08 ± 4.73 years (range, 1.4-12 years); the average follow-up duration was 20.17 ± 5.49 months. One patient had previously undergone open surgery. Four patients had gelastic seizures, one had gelastic and tonic seizures, and one had gelastic and generalized tonic-clonic seizures. The number of implanted electrodes ranged from 3 to 7, with an average of 5.33. One patient had transient diabetes insipidus after the operation, and no child had fever or new hormone metabolisms disorder after surgery. Four patients had Engel I classification outcomes (free from disabling seizures), and two patients had Engel II classification outcomes. Although the exploration of epileptic activity and the extent of ablation are limited by the number of SEEG electrodes for the complete disconnection. One-stage high-density focal stereo-array SEEG-guided radiofrequency was safe and effective for treating pediatric giant HH patients. It can be an alternative method to treat giant HHs where LITT is unavailable.
巨大下丘脑错构瘤(HHs)是极其罕见的病变,其治疗具有挑战性。虽然诸如射频热凝和激光消融等微创治疗改善了癫痫发作的预后,但通常需要多次手术。本研究探讨了基于立体定向脑电图(SEEG)的一期立体阵列射频热凝治疗小儿巨大HHs的价值。我们分析了2017年11月至2019年4月期间接受立体定向电极植入的6例巨大HHs(最大直径>30mm的肿块)患者的临床资料。经过多学科讨论,我们设计了一种高密度局灶性立体阵列电极植入策略。在同一电极的两个相邻触点之间,或不同电极的两个相邻触点之间进行SEEG引导下的双极凝固。6例患者中,男性3例,女性3例,平均年龄5.08±4.73岁(范围1.4 - 12岁);平均随访时间为20.17±5.49个月。1例患者曾接受过开颅手术。4例患者有痴笑发作,1例有痴笑和强直发作,1例有痴笑和全身强直阵挛发作。植入电极数量为3至7根,平均5.33根。1例患者术后出现短暂性尿崩症,术后无患儿发热或出现新的激素代谢紊乱。4例患者达到Engel I级分类结果(无致残性癫痫发作),2例患者达到Engel II级分类结果。尽管癫痫活动的探索和消融范围受SEEG电极数量限制,无法实现完全切断。一期高密度局灶性立体阵列SEEG引导下的射频治疗小儿巨大HHs患者安全有效。在无法进行激光间质热疗(LITT)的情况下,它可以作为治疗巨大HHs的替代方法。