Maamar M, Rahmani M, Aidi S, Benabdeljlil M, El Hassani My R, Jiddane M, Hicham Ch, El Alaoui-Faris M
Service de Neurologie A et de Neuropsychologie, Hôpital des Spécialités, CHU Ibn Sina, Rabat, Morocco.
Rev Neurol (Paris). 2007 Sep;163(8-9):809-16. doi: 10.1016/s0035-3787(07)91463-0.
Sneddon's syndrome is a rare disease defined by the presence of ischemic cerebrovascular events associated with livedo reticularis. We report a retrospective study of fifteen cases, thirteen women and two men, mean age of 37.93+/-9.77 years. All patients presented one or more cerebral infarcts. Six patients had dementia. Brain magnetic resonance imaging showed several cortical infarcts with white matter involvement. Cerebral angiography performed in all patients, showed a distal arteriopathy in twelve and thrombosis of the right carotid internal artery in one. One patient had antiphospholipid antibodies. Ten patients were treated with antiplatelet agents and five with anticoagulants. The course was favorable in eight patients and stationary in three. Four patients had several recurrent infarcts, one when anticoagulants were discontinued, one taking an anti-sludge-platelet agent and two who were not initially taking any treatment.
斯内登综合征是一种罕见疾病,其定义为存在与网状青斑相关的缺血性脑血管事件。我们报告了一项对15例患者的回顾性研究,其中13名女性和2名男性,平均年龄为37.93±9.77岁。所有患者均出现一处或多处脑梗死。6例患者患有痴呆症。脑部磁共振成像显示多处皮质梗死并累及白质。所有患者均进行了脑血管造影,其中12例显示远端动脉病变,1例显示右颈内动脉血栓形成。1例患者存在抗磷脂抗体。10例患者接受抗血小板药物治疗,5例接受抗凝治疗。8例患者病情好转,3例病情稳定。4例患者出现多次复发性梗死,1例在停用抗凝剂时出现,1例在服用抗血小板聚集剂时出现,2例最初未接受任何治疗。