Gupta Ajay, Raja Shankar, Kotagal Prakash, Lachhwani Deepak, Wyllie Elaine, Bingaman William B
Department of Neurology, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
Pediatr Neurol. 2004 Aug;31(2):89-95. doi: 10.1016/j.pediatrneurol.2004.01.008.
We studied the usefulness of ictal single-photon emission computed tomography in the presurgical evaluation of children with partial epilepsy resulting from focal cortical dysplasia. Fifteen children, age 1-18 years, were identified with partial epilepsy caused by focal cortical dysplasia (confirmed by histology) who underwent subtraction ictal single-photon emission computed tomography during presurgical evaluation. All children later underwent surgery at the Cleveland Clinic Epilepsy Center between 1996 and 2000. The findings of ictal single-photon emission computed tomography and brain positron emission tomography were classified as localized when "localizing and concordant" with the surgical resection site, nonconcordant when "localizing but not concordant" with the surgical resection, or nonlocalized when "no well-localized region of ictal hyperperfusion was observed on the difference image". In 15 patients, age 1.5-18 years (median age 8 years), epilepsy was classified as frontal in 7, posterior temporal/occipital in 3, temporal in 2, multilobar in 2, and parietal in 1. Of 15 patients, preoperative magnetic resonance imaging revealed focal cortical dysplasia in 11, positron emission tomography was localized in 9, and ictal single-photon emission computed tomography was localized in 8 patients. In 4 patients with normal magnetic resonance imaging but scalp electroencephalographic findings of partial epilepsy, ictal single-photon emission computed tomography and positron emission tomography were localized in 3 each. Fourteen patients were monitored for 6-39 months (mean 20 months). Six of 7 patients (85%) with localized ictal single-photon emission computed tomography compared with 4 of 7 (57%) with nonconcordant/nonlocalized ictal single-photon emission computed tomography had no seizures at follow-up. In 4 patients with normal magnetic resonance imaging, 3 patients with localized ictal single-photon emission computed tomography were free of seizures compared with 1 with nonconcordant ictal single-photon emission computed tomography who continued to have seizures. Ictal single-photon emission computed tomography is a useful adjunctive test in presurgical evaluation of children with refractory partial epilepsy due to focal cortical dysplasia, especially when brain magnetic resonance imaging is normal.
我们研究了发作期单光子发射计算机断层扫描在局灶性皮质发育不良所致儿童部分性癫痫术前评估中的作用。15名年龄在1至18岁的儿童,被确诊为由局灶性皮质发育不良引起的部分性癫痫(经组织学证实),他们在术前评估期间接受了减影发作期单光子发射计算机断层扫描。所有儿童后来于1996年至2000年间在克利夫兰诊所癫痫中心接受了手术。发作期单光子发射计算机断层扫描和脑正电子发射断层扫描的结果,当与手术切除部位“定位且一致”时被分类为定位性,当与手术切除“定位但不一致”时为非一致性,或当在差异图像上“未观察到发作期高灌注的明确定位区域”时为非定位性。15例患者,年龄1.5至18岁(中位年龄8岁),癫痫分类为额叶7例,颞后/枕叶3例,颞叶2例,多叶2例,顶叶1例。15例患者中,术前磁共振成像显示11例存在局灶性皮质发育不良,正电子发射断层扫描定位9例,发作期单光子发射计算机断层扫描定位8例。4例磁共振成像正常但头皮脑电图有部分性癫痫表现的患者,发作期单光子发射计算机断层扫描和正电子发射断层扫描各定位3例。14例患者接受了6至39个月(平均20个月)的监测。发作期单光子发射计算机断层扫描定位的7例患者中有6例(85%)在随访时无癫痫发作,而非一致性/非定位性发作期单光子发射计算机断层扫描的7例患者中有4例(57%)无癫痫发作。在4例磁共振成像正常的患者中,发作期单光子发射计算机断层扫描定位的3例患者无癫痫发作,而非一致性发作期单光子发射计算机断层扫描的1例患者仍有癫痫发作。发作期单光子发射计算机断层扫描在对局灶性皮质发育不良所致难治性部分性癫痫儿童的术前评估中是一种有用的辅助检查,尤其是当脑磁共振成像正常时。