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Cranial Magnetic Resonance Imaging Findings in Patients with Neuro-Behcet's Syndrome

机译:神经-贝塞特氏综合征患者的颅核磁共振成像结果

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OBJECTIVE: Behcet’s disease is a multisystemic, vascular-inflammatory disease of unknown origin. Impairment of the central nervoussystem is rare, and young adults can present with brain stem syndrome or hemiparesis. In this study, we aimed to determine the cranialmagnetic resonance imaging (MRI) patterns in patients diagnosed as parenchymal or nonparenchymal neuro-Behcet’s syndromewho did not have headache.METHODS: Thirty-eight patients admitted to the Haydarpasa Numune Training and Research Hospital, Department of1st Neurology and GATA Haydarpasa Training Hospital Neurology Department, Istanbul between 2003 and 2009 in the acute periodand with the diagnosis of neuro-Behcet’s syndrome were investigated. All the patients were examined by routine hematologicaland biochemical blood tests, vasculitis tests, cranial MRI, and magnetic resonance venography if needed. Patients with headache andthose without cranial MRI lesions were excluded.RESULTS: Eighteen patients, with a mean age of 34.6 ± 9.7 and age range of 17-51, were investigated. Eleven of the patients weremale and seven were female. In 14 patients, the diagnosis of Behcet’s disease was present for 11.5 years, while four patients werenewly diagnosed after admission. The most common complaints were hemiparesis, dysarthria and diplopia due to the cranial nerveinvolvement. Twelve of the patients were admitted with the first attack, five with the second attack and one with the third attack inthe acute period. Sixteen patients with parenchymal neuro-Behcet’s syndrome had a total of 41 lesions, and the brain stem was themost common localization (55.6%). Of the two patients with nonparenchymal neuro-Behcet’s syndrome, thrombosis was observedin the superior sagittal sinus in one and in the transverse sinus in the other.CONCLUSION: Cranial MRI is a sensitive diagnostic technique for neuro-Behcet’s syndrome. MRI is a noninvasive diagnostic tool to confirmthe involvement of the central nervous system and has an important role in confirming the stage of the illness in Behcet’s disease.
机译:目的:白塞病是一种多系统性血管炎性疾病,来源不明。中枢神经系统的损伤很少见,年轻人会出现脑干综合症或偏瘫。在这项研究中,我们旨在确定被诊断为没有头痛的实质性或非实质性神经-贝塞特氏综合征的患者的颅骨磁共振成像(MRI)模式。方法:38例入选了Haydarpasa Numune训练和研究医院第一科的患者神经病学和GATA Haydarpasa培训医院神经病学部门,伊斯坦布尔,于2003年至2009年之间,在急性期进行了诊断并诊断为神经性贝塞特综合症。所有患者均接受常规血液学和生化血液检查,血管炎检查,颅MRI和磁共振静脉造影检查。结果:18例平均年龄为34.6±9.7,年龄范围为17-51岁的患者被排除在外。患者中有11名是男性,而7名是女性。在14例患者中,白塞病的诊断持续了11.5年,而入院后又新诊断出4例患者。最常见的主诉是由于颅神经受累引起的偏瘫,构音障碍和复视。在急性期中,有12名患者首次发作入院,第二次发作入院5例,第三次发作入院。实质性神经-贝塞特综合征的16例患者共有41个病灶,其中脑干是最常见的部位(55.6%)。在两名非实质性神经-贝塞特氏综合症患者中,其中一个在上矢状窦中观察到血栓形成,而在另一侧在横窦中观察到血栓形成。 MRI是确认中枢神经系统受累的一种非侵入性诊断工具,在确定Behcet病的疾病阶段中具有重要作用。

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