Colombo Nadia, Tassi Laura, Galli Carlo, Citterio Alberto, Lo Russo Giorgio, Scialfa Giuseppe, Spreafico Roberto
Department of Neuroradiology, Ospedale Cà Granda Niguarda, Milano, Italy.
AJNR Am J Neuroradiol. 2003 Apr;24(4):724-33.
Focal cortical dysplasia (FCD) covers a spectrum of conditions in which the neuropathologic and electroclinic presentations and the surgical outcomes vary. The aim of this study was to identify the MR features of histologic subtypes of FCD that would be useful for differential diagnosis.
We reviewed the MR data of 49 patients treated surgically for intractable partial epilepsy, who received a histologic diagnosis of FCD not associated with other brain abnormalities except hippocampal sclerosis and who were classified by histologic criteria as having architectural dysplasia (28 patients), cytoarchitectural dysplasia (six patients), or Taylor's FCD (15 patients).
From the MR features, it was generally possible to distinguish Taylor's FCD from architectural or cytoarchitectural dysplasias (non-Taylor's FCD). Findings suggesting Taylor's FCD were focal cortical thickening, blurring of the gray-white matter junction, and hyperintensity (on T2-weighted images) of subcortical white matter often tapering toward the ventricle. Focal brain hypoplasia with shrinkage and moderate signal intensity alterations in the white matter core were present in most patients with architectural dysplasia. The lesion was generally extratemporal in Taylor's FCD and temporal in architectural dysplasia. Ipsilateral hippocampal sclerosis was often present in architectural dysplasia (dual abnormality).
In patients with FCD, Taylor's FCD and non-Taylor's FCD can usually be distinguished with MR imaging, although some overlap exists. A provisional MR diagnosis is important for presurgical investigations and surgical planning and may have prognostic implications.
局灶性皮质发育不良(FCD)涵盖了一系列疾病,其神经病理学、电临床特征及手术结果各不相同。本研究旨在确定FCD组织学亚型的磁共振成像(MR)特征,以助于鉴别诊断。
我们回顾了49例因药物难治性部分性癫痫接受手术治疗患者的MR数据,这些患者经组织学诊断为FCD,且除海马硬化外无其他脑异常,并根据组织学标准分为结构发育异常(28例)、细胞结构发育异常(6例)或泰勒型FCD(15例)。
从MR特征来看,通常可以将泰勒型FCD与结构或细胞结构发育异常(非泰勒型FCD)区分开来。提示泰勒型FCD的表现为局灶性皮质增厚、灰白质交界模糊以及皮质下白质在T2加权像上呈高信号,且常向脑室逐渐变细。大多数结构发育异常患者存在局灶性脑发育不全伴脑萎缩以及白质核心中等信号强度改变。泰勒型FCD的病灶通常位于颞叶外,而结构发育异常的病灶位于颞叶。结构发育异常患者常伴有同侧海马硬化(双重异常)。
在FCD患者中,虽然存在一些重叠,但通常可以通过MR成像区分泰勒型FCD和非泰勒型FCD。初步的MR诊断对于术前评估和手术规划很重要,并且可能具有预后意义。