Hwang P A, Otsubo H, Koo B K, Gilday D L, Chuang S H, Jay V, Hoffman H J
Department of Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada.
Pediatr Neurol. 1996 Apr;14(3):220-5. doi: 10.1016/0887-8994(96)00084-7.
This ongoing study examines abnormalities of cerebral perfusion in a consecutive series of children with infantile spasms and correlates cerebral blood flow (CBF) abnormalities with electroencephalographic (EEG), neuroimaging, and pathologic findings. A consecutive series of children with infantile spasms, diagnosed by standard clinical and EEG criteria, had cerebral perfusion studies using 99Tc-HmPAO single photon emission computed tomography (SPECT), together with neuroimaging studies using computed tomography (CT) and/or magnetic resonance imaging (MRI), interpreted independently and correlated with surgical pathologic findings. Twenty children aged 2-13 months (mean 9.3 months) were studied over a 4-year period; 60% had symptomatic infantile spasms due to cerebral dysgenesis (33%), other congenital lesions (25%), tuberous sclerosis (17%), or other causes (25%), and the remaining patients were cryptogenic (40%). CBF abnormalities were present in 85%: multifocal decrease (40%), focal increase (25%), diffuse decrease (15%), and focal increase (10%), while the remaining 15% had normal cerebral blood flow. Focal cortical lesions may lead to infantile spasms, even in cryptogenic patients diagnosed by functional neuroimaging such as 99Tc-HmPAO SPECT. In selected patients, surgical excision of the cortical lesions leads to improved seizure control and possibly outcome. The localization and surgical excision of focal cortical lesions in infantile spasms required further investigation with functional and structural neuroimaging, EEG, and intraoperative electrocorticography.
这项正在进行的研究对一系列连续性的婴儿痉挛症患儿的脑灌注异常进行了检查,并将脑血流量(CBF)异常与脑电图(EEG)、神经影像学及病理检查结果进行关联。一系列经标准临床和EEG标准诊断为婴儿痉挛症的患儿接受了使用99Tc-HmPAO单光子发射计算机断层扫描(SPECT)的脑灌注研究,同时还进行了使用计算机断层扫描(CT)和/或磁共振成像(MRI)的神经影像学研究,这些研究由独立人员解读,并与手术病理结果相关联。在4年期间对20名年龄在2至13个月(平均9.3个月)的儿童进行了研究;60%的患儿因脑发育异常(33%)、其他先天性病变(25%)、结节性硬化症(17%)或其他原因(25%)患有症状性婴儿痉挛症,其余患者为隐源性(40%)。85%的患儿存在CBF异常:多灶性减少(40%)、局灶性增加(25%)、弥漫性减少(15%)和局灶性增加(10%),而其余15%的患儿脑血流正常。局灶性皮质病变可能导致婴儿痉挛症,即使在通过功能性神经影像学如99Tc-HmPAO SPECT诊断为隐源性的患者中也是如此。在部分患者中,手术切除皮质病变可改善癫痫控制情况,并可能改善预后。婴儿痉挛症中局灶性皮质病变的定位及手术切除需要通过功能性和结构性神经影像学、EEG及术中皮质脑电图进行进一步研究。