Kurwale Nilesh S, Patil Sandip B, Jagtap Sujit A, Joshi Aniruddha, Deshmukh Yogeshwari, Nilegaonkar Sujit, Bapat Deepa, Chitnis Sonal, Wadhwani Nayan
Department of Neurosurgery, Deenanath Mangeshkar Hospital, Pune, India; Department of Neurosurgery, D. Y. Patil Medical College, Pune, India.
Department of Neurology, Deenanath Mangeshkar Hospital, Pune, India.
Epilepsy Res. 2021 Sep;175:106703. doi: 10.1016/j.eplepsyres.2021.106703. Epub 2021 Jun 25.
To study surgical outcomes in pharmaco-resistant epilepsy associated with posterior cortex ulegyria secondary to perinatal insults.
A cohort was analysed for clinico-radiological charectaristics, surgical interventions and seizure outcomes.
A total of 38 patients underwent surgery, divided as group A - curative surgeries (n = 20) and group B - palliative surgeries (n = 18). Mean age of onset of epilepsy in group A was 5.2 ± 3.4 years against 2.7 ± 2.4 years in group B (p < 0.01). Electroclinical Lennox Gastaut Syndrome was encountered in 9/20 patients in group A, against all 18 patients in group B. Disabling reflex epilepsy was seen in 10 (26 %) patients. Interictal electrophysiology localized in the posterior cortex in all patients in group A, but ictal onsets contributed in only 7/20 patients. Nine patients from group A had unilateral parieto-occipital ulegyria while bilateral in 11/20 patients, and 16/18 from group B. Group A patients underwent parieto-occipital resection (n = 10) and temporo-parieto-occipital disconnection (n = 10) while group B underwent complete corpus callosotomy (n = 18). In group A, Engel Ia outcome was achieved in 15/20 patients (75 %) at mean follow up of 23.5 ± 7.9 months. Group B patients experienced cessation of head drops in all 18 patients, with two-third reduction in seizure frequency at 29.2± 12.4 months of mean follow up. Reflex seizures responded completely in both groups.
Epilepsy surgeries for posterior cortex ulegyria results in excellent seizure outcomes. Corpus callosotomy appears highly effective as a palliation for head drop as well as disabling reflex seizures in a well selected cohort.
研究围产期损伤继发的后皮质脑回发育不全所致药物难治性癫痫的手术疗效。
分析一组患者的临床放射学特征、手术干预措施和癫痫发作结果。
共有38例患者接受了手术,分为A组——根治性手术(n = 20)和B组——姑息性手术(n = 18)。A组癫痫发作的平均发病年龄为5.2±3.4岁,而B组为2.7±2.4岁(p < 0.01)。A组20例患者中有9例出现电临床Lennox - Gastaut综合征,而B组18例患者均出现该综合征。10例(26%)患者出现致残性反射性癫痫。A组所有患者发作间期电生理定位于后皮质,但发作期起始仅见于20例中的7例。A组9例患者为单侧顶枕叶脑回发育不全,11/20例患者为双侧,B组16/18例患者为双侧。A组患者接受了顶枕叶切除术(n = 10)和颞顶枕叶离断术(n = 10),而B组接受了完全胼胝体切开术(n = 18)。A组中,20例患者中有15例(75%)在平均随访23.5±7.9个月时达到Engel Ia级结果。B组18例患者均停止了点头发作,在平均随访29.2±12.4个月时癫痫发作频率降低了三分之二。两组反射性癫痫均完全缓解。
后皮质脑回发育不全的癫痫手术可取得优异的癫痫发作控制效果。胼胝体切开术在精心挑选的队列中作为缓解点头发作和致残性反射性癫痫的方法似乎非常有效。