Houman Mohamed-Habib, Bellakhal Syrine, Ben Salem Thouraya, Hamzaoui Amira, Braham Amel, Lamloum Mounir, Monia Smiti-Khanfir, Ben Ghorbel Imed
Department of Internal Medicine, La Rabta University Hospital, Faculty of Medicine of Tunis, university el Manar, 1007 Tunis, Tunisia.
Clin Neurol Neurosurg. 2013 Oct;115(10):2015-8. doi: 10.1016/j.clineuro.2013.06.009. Epub 2013 Jul 3.
The aim of the present study was to analyze demographic, clinical and genetic features of Behçet's disease patients with neurological involvement through a monocentric study of a homogenous group of hospitalized patients observed in the same department and to compare them with those of other ethnic and geographic groups.
Four hundred and thirty Behçet's disease (BD) patients were retrospectively studied. Diagnosis of BD was made according to the international study group for Behçet's disease criteria. Patients with neurological findings suggestive of involvement of the nervous system by BD were further studied according to clinical examination, laboratory tests and neuroradiological investigations.
Neurological involvement was observed in 121 patients (28.1%). The mean age at neuro-Behçet's disease (NBD) onset was 29.7 years. Average disease duration of BD before neurological manifestations onset was 6.4 years. Male to female ratio was 1.8. Of the 121 NBD patients, parenchymal involvement occurred in 74 patients (61%). Among them 26 (21.4%) presented with brainstem involvement, 24 (19.8%) with hemispheric involvement and 2 (1.6%) with spinal cord involvement. Non-parenchymal NBD occurred in 47 patients (39%). Involvement of the main vascular structures (Vasculo-NBD) was the most common non-parenchymal NBD lesion found in 35 patients (28.9%) consisting of cerebral vein thrombosis (CVT) in 24 cases and cerebral arterial thrombosis in 11 cases. Forty-nine (40.5%) patients with NBD have been followed-up for a median of 3 years (range 1-19 years). Forty-one of them recovered well without significant residual disability, 5 patients made no improvement and are left with severe neurological impairments and 3 died. Male gender and CNS parenchymal lesions occurrence were significantly associated with a poorer prognosis.
Clinical and epidemiological features of NBD are various. In our Tunisian cohort of NBD patients the main characteristic features were male predominance, a relatively high prevalence of CVT, a low prevalence of intra-cranial hypertension and a significant lower frequency of HLA-B51 haplotype.
本研究旨在通过对同一科室观察的一组同质化住院患者进行单中心研究,分析神经受累的白塞病患者的人口统计学、临床和遗传特征,并将其与其他种族和地理群体的特征进行比较。
对430例白塞病(BD)患者进行回顾性研究。BD的诊断依据国际白塞病研究组标准。根据临床检查、实验室检查和神经放射学检查,对提示神经系统受累的BD患者进行进一步研究。
121例患者(28.1%)出现神经受累。神经白塞病(NBD)发病的平均年龄为29.7岁。神经系统表现出现前BD的平均病程为6.4年。男女比例为1.8。在121例NBD患者中,74例(61%)出现实质受累。其中26例(21.4%)表现为脑干受累,24例(19.8%)表现为半球受累,2例(1.6%)表现为脊髓受累。47例(39%)患者出现非实质NBD。主要血管结构受累(血管性NBD)是最常见的非实质NBD病变,35例(28.9%)患者出现,其中24例为脑静脉血栓形成(CVT),11例为脑动脉血栓形成。49例(40.5%)NBD患者接受了中位3年(范围1 - 19年)的随访。其中41例恢复良好,无明显残留残疾,5例无改善,遗留严重神经功能障碍,3例死亡。男性和中枢神经系统实质病变的发生与较差的预后显著相关。
NBD的临床和流行病学特征各不相同。在我们的突尼斯NBD患者队列中,主要特征为男性占主导、CVT患病率相对较高、颅内高压患病率较低以及HLA - B51单倍型频率显著较低。