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Incidental parenchymal magnetic resonance imaging findings in the brains of patients with neurofibromatosis type 2

机译:神经纤维瘤患者患者的偶然实质磁共振成像结果2

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Purpose Whereas T2 hyperintensities known as NF-associated bright spots are well described in patients with neurofibromatosis type I (NF-1), there is a paucity of data on incidental findings in patients with neurofibromatosis type II (NF-2). We aim to characterize unexplained imaging findings in the brains of patients with NF-2. Materials and methods This study is retrospective, HIPAA-compliant and approved by the institutional review board. 34 patients with NF-2 underwent brain magnetic resonance imaging (MRI) between January 2000 and December 2012. T2 and T1-weighted imaging characteristics, diffusion weighted imaging (DWI) characteristics, and enhancement patterns were analyzed by visual inspection. Clinical information at time of imaging was available for all patients. Neuropathologic data was available for one patient. Results We found unexplained T2 hyperintensities present on initial imaging in 23/34 patients (67%). Of the 23 patients with unexplained MRI findings, 15 (65%) had wedge-shaped T2 hyperintensities in the subcortical white matter extending to the cortex suggestive of a cortical dysplasia. 3 additional cases (17%) had a lesion within the cerebellum suggestive of a neuronal migration anomaly. In one patient where the MRI was suggestive of focal cortical dysplasia, histopathologic analysis revealed dysplastic glial foci without other alterations of cortical architecture or other cytologic abnormalities. Conclusion Unexplained T2 hyperintensities occur frequently in patients with NF-2. While they may not be the NF-2 equivalent of NF-associated bright spots seen in NF-1, some of these T2 hyperintensities in patients with NF-2 may represent underlying disorders of neuronal migration. Further studies are needed to validate our findings. Highlights ? 34 patients with NF2 underwent consecutive brain magnetic resonance imaging (MRI). ? 67% had brain MRI findings suggestive of a focal cortical dysplasia. ? 17% had a lesion within the cerebellum suggestive of a neuronal migration anomaly. ? One patient was found to have micro-hamartomas involving the cortex. ? Patients with NF-2 may have radiographic findings suggestive of cortical dysplasia.
机译:目的,而神经纤维瘤病患者(NF-1)的患者,T2被称为NF相关亮点的高原性质,缺乏神经纤维瘤病患者II型(NF-2)的偶然调查结果。我们的目标是在NF-2患者的大脑中表征原因的成像发现。材料和方法本研究是回顾性的,符合机构审查委员会的批准和批准。 34患者在2012年1月至2012年1月至12月之间进行了NF-2的脑磁共振成像(MRI)。通过目视检查分析了T2和T1加权成像特性,扩散加权成像(DWI)特性和增强模式。所有患者都有成像时的临床信息。神经病理数据可用于一名患者。结果我们发现在23/34名患者(67%)的初始成像上存在未解释的T2高原。在23例未解释的MRI发现的患者中,15例(65%)在延伸到皮质发育不良的皮层延伸的皮质白质中,具有楔形T2高原。 3额外的病例(17%)在小脑中有一个病变,暗示神经元迁移异常。在患有局灶性皮质发育不良的MRI暗示的患者中,组织病理学分析显示出消化不良胶质灶,没有其他改变皮质结构或其他细胞异常。结论NF-2患者经常发生不明原因的T2高原。虽然它们可能不是NF-1所见的NF-2当量,但NF-2患者中的一些这些T2高原可能代表神经元迁移的基本疾病。需要进一步的研究来验证我们的研究结果。强调 ? 34例NF2患者接受连续脑磁共振成像(MRI)。 ? 67%的脑MRI调查结果暗示了局灶性皮质发育不良。 ? 17%的小脑内部存在病变,暗示神经元迁移异常。 ?发现一个患者有涉及皮质的微小流氓瘤。 ? NF-2的患者可能有放射线摄影结果,提示皮质发育不良。

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