Type II Focal Cortical Dysplasia: Ex Vivo 7T Magnetic Resonance Imaging Abnormalities and Histopathological Comparisons

被引:63
作者
Zucca, Ileana [2 ]
Milesi, Gloria [1 ]
Medici, Valentina [1 ]
Tassi, Laura [3 ]
Didato, Giuseppe [1 ]
Cardinale, Francesco [3 ]
Tringali, Giovanni [4 ]
Colombo, Nadia [5 ]
Bramerio, Manuela [6 ]
D'Incerti, Ludovico [7 ]
Freri, Elena [8 ]
Morbin, Michela [9 ]
Fugnanesi, Valeria [9 ]
Figini, Matteo [2 ]
Spreafico, Roberto [1 ]
Garbelli, Rita [1 ]
机构
[1] C Besta Neurol Inst Fdn, Clin Epileptol & Expt Neurophysiol Unit, Via Amadeo 42, I-20133 Milan, Italy
[2] C Besta Neurol Inst Fdn, Dept Sci, I-20133 Milan, Italy
[3] Osped Niguarda Ca Granda, C Munari Epilepsy Surg Ctr, Milan, Italy
[4] C Besta Neurol Inst Fdn, Neurosurg Unit, I-20133 Milan, Italy
[5] Osped Niguarda Ca Granda, Dept Neuroradiol, Milan, Italy
[6] Osped Niguarda Ca Granda, Dept Pathol, Milan, Italy
[7] C Besta Neurol Inst Fdn, Neuroradiol Unit, I-20133 Milan, Italy
[8] C Besta Neurol Inst Fdn, Dept Pediat Neurosci, I-20133 Milan, Italy
[9] C Besta Neurol Inst Fdn, Neurol & Neuropathol 5, I-20133 Milan, Italy
关键词
SURGICAL-TREATMENT; MRI; EPILEPSY; CLASSIFICATION; MALFORMATIONS; SCLEROSIS; FEATURES; OUTCOMES; ENTITY; CORTEX;
D O I
10.1002/ana.24541
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: In the present report, the correlations between ex vivo high-resolution imaging and specific histological and ultrastructural patterns in type II focal cortical dysplasia (FCD) have been studied to explain the differences in the magnetic resonance imaging (MRI) detection of dysplasia and to contribute to the presurgical imaging evaluation of this pathology. Methods: Surgical specimens from 13 patients with FCD IIa/b were submitted to 7T MRI scanning, and then analyzed histologically and ultrastructurally to compare the results with the MRI findings. Region of interest (ROI)-based measures on T2-weighted images (T2wi) were quantitatively evaluated in the lesion and in adjacent perilesional gray and white matter. Results: Matched histological sections and 7T T2wi showed that the core of the lesion was characterized by patchy aggregates of abnormal cells and fiber disorganization related to inhomogeneity of intracortical signal intensity. The quantitative approach on T2wi can help to distinguish the lesions and perilesional areas even in a clinical MRI-negative case. The ultrastructural study showed that the strong signal hyperintensity in the white matter of FCD IIb was related to a dysmyelination process associated with severe fiber loss and abnormal cells. Less severe histopathological features were found in FCD IIa, thus reflecting their less evident MRI alterations. Interpretation: We suggest that white matter abnormalities in type IIb FCD are due to defects of the myelination processes and maturation, impaired by the presence of balloon cells. To reveal the presence and the border of type II cortical dysplasia on MRI, a quantitative ROI-based analysis (coefficient of variation) is also proposed.
引用
收藏
页码:42 / 58
页数:17
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