Grygiel-Górniak B, Puszczewicz M, Czaplicka E
Department of Rheumatology and Internal Medicine, Poznan University of Medical Sciences, Poznan, Poland.
Eur Rev Med Pharmacol Sci. 2015;19(9):1729-35.
Susac syndrome is an uncommon autoimmune microangiopathy characterized mainly by neurological disorders and, to date, 304 clinical cases have been described. The background of this syndrome is an immune-mediated endotheliopathy that affects the microvasculature of the brain, retina, and inner ear resulting in encephalopathy, hearing loss, and branch retinal artery occlusions. However, the cause and the pathogenesis of this microangiopathy remain unclear. Magnetic resonance imaging, retinal fluorescein angiography, and audiography findings enable the diagnosis of this syndrome. In this review, we have demonstrated the epidemiology and pathology of Susac syndrome with detailed description of clinical signs, diagnostic procedures and therapeutic possibilities.
Susac综合征是一种罕见的自身免疫性微血管病,主要特征为神经功能障碍,迄今为止,已报道了304例临床病例。该综合征的背景是一种免疫介导的内皮病变,影响脑、视网膜和内耳的微血管,导致脑病、听力丧失和视网膜分支动脉阻塞。然而,这种微血管病的病因和发病机制仍不清楚。磁共振成像、视网膜荧光血管造影和听力检查结果有助于诊断该综合征。在本综述中,我们阐述了Susac综合征的流行病学和病理学,并详细描述了临床症状、诊断方法和治疗可能性。