Imaging of Patients with Hippocampal Sclerosis at 7 Tesla: Initial Results

被引:38
作者
Breyer, Tobias [1 ]
Wanke, Isabel [1 ]
Maderwald, Stefan [2 ]
Woermann, Friedrich G. [3 ]
Kraff, Oliver [2 ]
Theysohn, Jens M. [1 ]
Ebner, Alois
Forsting, Michael [1 ]
Ladd, Mark E. [2 ]
Schlamann, Marc [2 ,3 ]
机构
[1] Essen Univ Hosp, Dept Diagnost & Intervent Radiol & Neuroradiol, D-45122 Essen, Germany
[2] Univ Duisburg Essen, Erwin L Hahn Inst Magnet Resonance Imaging, Essen, Germany
[3] Bethel Epilepsy Ctr, MRI & Klink Mara, Bielefeld, Germany
关键词
High resolution MRI; 7; Tesla; hippocampal sclerosis; human; TEMPORAL-LOBE EPILEPSY; FEBRILE SEIZURES; T2; RELAXOMETRY; MR-IMAGES; PATHOLOGY; CONSEQUENCE; SECTIONS; SURGERY;
D O I
10.1016/j.acra.2009.10.013
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Rationale and Objectives: Focal epilepsies potentially can be cured by neurosurgery; other treatment options usually remain symptomatic. High-resolution magnetic resonance (MR) imaging is the central imaging strategy in the evaluation of focal epilepsy. The most common substrate of temporal epilepsies is hippocampal sclerosis (HS), which cannot always be sufficiently characterized with current MR field strengths. Therefore, the purpose of our study was to demonstrate the feasibility of high-resolution MR imaging at 7 Tesla in patients with focal epilepsy resulting from a HS and to improve image resolution at 7 Tesla in patients with HS. Materials and Methods: Six patients with known HS were investigated with T1-, T2-, T2*-, and fluid-attenuated inversion recovery-weighted sequences at 7 Tesla with an eight-channel transmit-receive head coil. Total imaging time did not exceed 90 minutes per patient. Results: High-resolution imaging at 7 Tesla is feasible and reveals high resolution of intrahippocampal structures in vivo. HS was confirmed in all patients. The maximum non-interpolated in-plane resolution reached 0.2 x 0.2 mm(2) in T2*-weighted images. The increased susceptibility effects at 7 Tesla revealed identification of intrahippocampal structures in more detail than at 1.5 Tesla, but otherwise led to stronger artifacts. Imaging revealed regional differences in hippocampal atrophy between patients. The scan volume was limited because of specific absorption rate restrictions, scanning time was reasonable. Conclusions: High-resolution imaging at 7 Tesla is promising in presurgical epilepsy imaging. "New" contrasts may further improve detection of even very small intrahippocampal structural changes. Therefore, further investigations will be necessary to demonstrate the potential benefit for presurgical selection of patients with various lesion patterns in mesial temporal epilepsies resulting from a unilateral HS.
引用
收藏
页码:421 / 426
页数:6
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