Jea Andrew, Vachhrajani Shobhan, Johnson Keyne K, Rutka James T
Division of Pediatric Neurosurgery, Department of Neurosurgery, Baylor College of Medicine, Houston, Texas, USA.
Neurosurg Focus. 2008 Sep;25(3):E7. doi: 10.3171/FOC/2008/25/9/E7.
Although corpus callosotomy has been used effectively since the late 1930s to treat severe, medically intractable seizure disorders, particularly atonic or drop-attack seizures, controversy remains as to when, how, and how much surgery should be performed. Intraoperative determination of the extent of callosotomy, the need to stage the procedure, and the side of the interhemispheric approach represent technical issues that remain debatable. The authors report the 12-year experience of the senior author as well as surgical outcomes with corpus callosotomy using a frameless stereotactic neuronavigation system (ISG View Wand and BrainLab).
Thirteen consecutive children at The Hospital for Sick Children underwent single-stage corpus callosotomy for medically intractable seizures. The mean age was 10.3 years. Five children underwent partial callosotomy, and 8 underwent complete callosotomy. The side of operative approach to avoid large parasagittal bridging veins was determined by preoperative study of 3D MR imaging/MR venography reconstructed by the neuronavigation system. The extent of callosotomy was determined using intraoperative feedback from the neuronavigation system and postoperative MR imaging.
The extent of callosotomy determined by intraoperative neuronavigation and postoperative MR imaging correlated closely in all cases. There were no operative deaths. There was no significant postoperative morbidity related to venous infarction. Four of 5 patients in the partial callosotomy cohort and 7 of 8 patients in the complete callosotomy cohort showed significant improvement in seizure control.
The use of frameless stereotactic neuronavigation is a safe, effective, and important surgical adjunct in the planning and execution of successful corpus callosotomy in children with intractable epilepsy.
尽管自20世纪30年代末以来,胼胝体切开术已被有效地用于治疗严重的、药物难治性癫痫发作障碍,尤其是失张力发作或跌倒发作,但对于何时、如何以及进行多少手术仍存在争议。术中确定胼胝体切开术的范围、是否需要分阶段进行手术以及半球间入路的一侧,这些技术问题仍有争议。作者报告了资深作者的12年经验以及使用无框架立体定向神经导航系统(ISG View Wand和BrainLab)进行胼胝体切开术的手术结果。
13名连续的患病儿童在病童医院接受了单阶段胼胝体切开术以治疗药物难治性癫痫发作。平均年龄为10.3岁。5名儿童接受了部分胼胝体切开术,8名接受了完全胼胝体切开术。通过神经导航系统重建的术前3D磁共振成像/磁共振静脉造影来确定避免大的矢状旁桥静脉的手术入路一侧。使用神经导航系统的术中反馈和术后磁共振成像来确定胼胝体切开术的范围。
术中神经导航和术后磁共振成像确定的胼胝体切开术范围在所有病例中密切相关。没有手术死亡。没有与静脉梗死相关的显著术后发病率。部分胼胝体切开术队列中的5名患者中有4名,完全胼胝体切开术队列中的8名患者中有7名在癫痫控制方面有显著改善。
在为患有难治性癫痫的儿童成功进行胼胝体切开术的规划和实施中,使用无框架立体定向神经导航是一种安全、有效且重要的手术辅助手段。