Kral T, von Lehe M, Podlogar M, Clusmann H, Süssmann P, Kurthen M, Becker A, Urbach H, Schramm J
Department of Neurosurgery, University of Bonn, Medical Centre, Sigmund Freud Strasse 25, 53105 Bonn, Germany.
J Neurol Neurosurg Psychiatry. 2007 Aug;78(8):853-6. doi: 10.1136/jnnp.2006.105361. Epub 2007 Feb 7.
Studies of long term outcome after epilepsy surgery for cortical malformations are rare. In this study, we report our experience with surgical treatment and year to year long term outcome for a subgroup of patients with focal cortical dysplasia (FCD).
We retrospectively analysed the records of 49 patients (females n = 26; males n = 23; mean age 25 (11) years) with a mean duration of epilepsy of 18 years (range 1-45). Preoperative MRI, histological results based on the Palmini classification and clinical year to year follow-up according to the International League Against Epilepsy (ILAE) classification were available in all patients.
98% of patients had a lesion on preoperative MRI. In addition to lobectomy (n = 9) or lesionectomy (n = 40), 14 patients had multiple subpial transections of the eloquent cortex. The resected tissue was classified as FCD type II b in 41 cases with an extratemporal (88%) and FCD type II a in 8 cases with a temporal localisation (100%). After a mean follow-up of 8.1 (4.5) years, 37 patients (76%) were seizure free, a subgroup of 23 patients (47%) had been completely seizure free since surgery (ILAE class 1a) and 4 patients (8%) had only auras (ILAE class 2). Over a 10 year follow-up, the proportion of satisfactory outcomes decreased, mainly within the first 3 years. During long term follow-up, 48% stopped antiepileptic drug treatment, 34% received a driver's license and 57% found a job or training.
Surgical treatment of epilepsy with FCD is not only successful in the short term but also has a satisfying long term outcome which remains constant after 3 years of follow-up but is not associated with better employment status or improvement in daily living.
关于皮质发育畸形癫痫手术后长期预后的研究很少。在本研究中,我们报告了我们对一组局灶性皮质发育不良(FCD)患者的手术治疗经验及逐年的长期预后情况。
我们回顾性分析了49例患者(女性26例;男性23例;平均年龄25(11)岁)的记录,这些患者癫痫平均病程为18年(范围1 - 45年)。所有患者均有术前MRI、基于帕尔米尼分类的组织学结果以及根据国际抗癫痫联盟(ILAE)分类进行的逐年临床随访资料。
98%的患者术前MRI有病变。除了肺叶切除术(9例)或病灶切除术(40例)外,14例患者对明确的皮质进行了多处软膜下横切术。切除组织在41例颞外病变(88%)中被分类为II b型FCD,在8例颞叶病变(100%)中被分类为II a型FCD。平均随访8.1(4.5)年后,37例患者(76%)无癫痫发作,23例患者(47%)自手术以来完全无癫痫发作(ILAE 1a级),4例患者(8%)仅有先兆(ILAE 2级)。在10年的随访中,满意结果的比例下降,主要在前3年内。在长期随访中,48%的患者停止了抗癫痫药物治疗,34%的患者获得了驾驶执照,57%的患者找到了工作或接受了培训。
FCD癫痫的手术治疗不仅在短期内成功,而且长期预后令人满意,随访3年后保持稳定,但与更好的就业状况或日常生活改善无关。