Seizure control outcomes after resection of dysembryoplastic neuroepithelial tumor in 50 patients Clinical article

被引:83
作者
Chang, Edward F. [1 ]
Christie, Catherine [1 ]
Sullivan, Joseph E. [2 ]
Garcia, Paul A. [2 ]
Thian, Tarik [3 ]
Gupta, Nalin [1 ]
Berger, Mitchel S. [1 ]
Barbaro, Nicholas M. [1 ]
机构
[1] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
关键词
dysembryoplastic neuroepithelial tumor; outcome; epilepsy; seizure; LONG-TERM SEIZURE; CORTICAL DYSPLASIA; MALIGNANT-TRANSFORMATION; EPILEPSY; CLASSIFICATION; DIAGNOSIS; FEATURES; CHILDREN;
D O I
10.3171/2009.8.PEDS09368
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Dysembryoplastic neuroepithelial tumors (DNETs) are a subset of relatively rare glioneuronal tumors that typically present with epilepsy during childhood. The authors' aim was to identify factors that predict seizure control following excision. Methods. The authors reviewed the cases of 50 patients who underwent resection of DNETs at the University of California, San Francisco, between 1990 and 2006. Demographic, seizure history, radiographic, and histopathological data were collected and analyzed for statistical association with postoperative seizure control. Results. Of the 50 patients, 86% presented with intractable epilepsy. The median age at surgery was 21 years (range 4-46 years; 40% were < 18 years old at time of surgery), with a median duration of 8 years from onset of seizures (24% were adult-onset seizures). Fifty-two percent of the cases were associated with adjacent focal cortical dysplasia. Complete resection was achieved in 78% of cases. Intraoperative electrocorticography in 23 patients identified extralesional interictal activity in 16 cases, which led to extended lesionectomy or lobectomy. The remaining patients underwent lesionectomy alone. The median follow-up was 5.6 years, during which time tumor progression occurred after subtotal resection. The proportional estimates of seizure freedom (Engel Class I outcome) were 0.86 at I year and 0.85 at 5 years. Seizure freedom was predicted by complete or extended resection (OR 1.68, 95% CI 1.39-2.03; p < 0.0001) and extratemporal location (OR 1.20, 95% CI 1.02-1.42; p = 0.03) on multivariate analysis. Secondary analysis for intraoperative electrocorticography cases demonstrated that seizure outcome was better when extralesional spiking foci were detected (94% seizure free) compared with when they were absent (43% seizure free). Conclusions. Excision of DNETs and, when present, adjacent dysplastic cortex was highly effective for seizure control. Excellent seizure-free outcomes and tumor control were seen with lesionectomy alone in most cases. Electrocorticography with extended resection was useful for patients with pharmacoresistant epilepsy. (DOI: 10.3171/2009.8.PEDS09368)
引用
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页码:123 / 130
页数:8
相关论文
共 30 条
[1]  
[Anonymous], 1981, Epilepsia, V22, P489
[2]   Glioneuronal tumors and medically intractable epilepsy: a clinical study with long-term follow-up of seizure outcome after surgery [J].
Aronica, E ;
Leenstra, S ;
van Veelen, CWM ;
van Rijen, PC ;
Hulsebos, TJ ;
Tersmette, AC ;
Yankaya, B ;
Troost, D .
EPILEPSY RESEARCH, 2001, 43 (03) :179-191
[3]   A developmental and genetic classification for malformations of cortical development [J].
Barkovich, AJ ;
Kuzniecky, RI ;
Jackson, GD ;
Guerrini, R ;
Dobyns, WB .
NEUROLOGY, 2005, 65 (12) :1873-1887
[4]   Surgery for epilepsy in children with dysembryoplastic neuroepithelial tumor: clinical spectrum, seizure outcome, neuroradiology, and pathology [J].
Bilginer, Burcak ;
Yalnizoglu, Dilek ;
Soylemezoglu, Figen ;
Turanli, Guzide ;
Cila, Aysenur ;
Topcu, Meral ;
Akalan, Nejat .
CHILDS NERVOUS SYSTEM, 2009, 25 (04) :485-491
[5]   Adult-onset epilepsy associated with dysembryoplastic neuroepithelial tumors [J].
Burneo, J. G. ;
Tellez-Zenteno, J. ;
Steven, D. A. ;
Niaz, N. ;
Hader, W. ;
Pillay, N. ;
Wiebe, S. .
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2008, 17 (06) :498-504
[6]   Long-term seizure outcome following surgery for dysembryoplastic neuroepithelial tumor [J].
Chan, CH ;
Bittar, RG ;
Davis, GA ;
Kalnins, RM ;
Fabinyi, GCA .
JOURNAL OF NEUROSURGERY, 2006, 104 (01) :62-69
[7]   Seizure characteristics and control following resection in 332 patients with low-grade gliomas [J].
Chang, Edward F. ;
Potts, Matthew B. ;
Keles, G. Evren ;
Lamborn, Kathleen R. ;
Chang, Susan M. ;
Barbaro, Nicholas M. ;
Berger, Mitchel S. .
JOURNAL OF NEUROSURGERY, 2008, 108 (02) :227-235
[8]   DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOR - A SURGICALLY CURABLE TUMOR OF YOUNG-PATIENTS WITH INTRACTABLE PARTIAL SEIZURES - REPORT OF 39 CASES [J].
DAUMASDUPORT, C ;
SCHEITHAUER, BW ;
CHODKIEWICZ, JP ;
LAWS, ER ;
VEDRENNE, C .
NEUROSURGERY, 1988, 23 (05) :545-556
[9]  
Engel Jerome Jr., 1993, P609
[10]  
Fernandez C, 2003, AM J NEURORADIOL, V24, P829