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Computed tomography and magnetic resonance appearance of sporadic meningioangiomatosis correlated with pathological findings.

机译:散发性脑膜血管瘤病的计算机体层摄影和磁共振外观与病理结果相关。

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PURPOSE: Meningioangiomatosis (MA) is a rare benign localized lesion of leptomeninges and underlying cerebral cortex. Preoperative diagnosis is difficult and challenging because of its diverse clinical, pathological, and imaging features. We retrospectively analyzed 7 cases of MA to explore their imaging features and correlate with pathological findings. MATERIALS AND METHODS: Imaging studies including computed tomography (CT) and magnetic resonance imaging (MRI) were retrospectively reviewed in 7 patients with surgically and pathologically verified intracranial MA (not associated with neurofibromatosis). Computed tomography studies were performed in axial plane without iodinated contrast-material administration; magnetic resonance studies consisted of axial T1-weighted, T2-weighted, Fluid attenuated Inversion Recovery (FLAIR), and postcontrast T1-weighted sequences and coronal or sagittal precontrast and postcontrast T1-weighted sequences. RESULTS: Computed tomography showed focal extensively calcified lesions in 3 cases, lesions with patchy calcification in 2 cases, and no apparent calcification in 2 cases. Magnetic resonance imaging demonstrated predominantly hypointensity on T1-weighted images and hyperintensity on T2-weighted images. Six of 7 cases exhibited gyriform hyperintensity on FLAIR sequences, which correlated with proliferating microvessels with perivascular cuffs of spindle-cell proliferation within the cortex on histopathological analysis. After contrast-material administration, all but 1 showed heterogeneous enhancement. The nonenhancing lesion on MRI was completely calcified on CT. CONCLUSION: Gyriform hyperintensity on FLAIR sequence is the main MRI feature of MA, which correlates with proliferating microvessels with perivascular cuffs of spindle-cell proliferation within the cortex on pathological analysis. Plain CT scan is essential to demonstrate the extent of calcification of these lesions.
机译:目的:脑膜血管瘤病(MA)是软脑膜和下层大脑皮质的一种罕见的良性局限性病变。由于其多样的临床,病理和影像学特征,术前诊断是困难且具有挑战性的。我们回顾性分析了7例MA,以探讨其影像学特征并与病理结果相关。材料与方法:回顾性分析了7例经手术和病理证实的颅内MA(与神经纤维瘤病无关)的患者的影像学研究,包括计算机断层扫描(CT)和磁共振成像(MRI)。计算机断层扫描研究是在轴向平面上进行的,无碘造影剂给药。磁共振研究包括轴向T1加权,T2加权,流体衰减反转恢复(FLAIR),造影剂T1加权序列以及冠状或矢状造影剂和造影剂T1加权序列。结果:计算机体层摄影术显示局灶性广泛钙化病变3例,钙化斑片状病变2例,无明显钙化病变2例。磁共振成像显示,T1加权图像主要表现为低血压,T2加权图像表现为高强度。 7例中有6例在FLAIR序列上表现出回旋状高强度,这与皮层中梭形细胞增殖的微血管增生相关,在组织病理学分析中。对比剂给药后,除1外,其余均显示异质性增强。 MRI上的非增强病变在CT上完全钙化。结论:FLAIR序列上的螺旋状高信号是MA的主要MRI特征,病理分析表明,其与皮层中梭形细胞增殖的血管周围的微血管增生有关。普通CT扫描对于证明这些病变的钙化程度至关重要。

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