Marrodan Mariano, Correale Jorge, Alessandro Lucas, Amaya Mariela, Fracaro Maria Eugenia, Köhler Alejandro Alfredo, Fiol Marcela
Department of Neurology, Institute for Neurological Research Dr. Raúl Carrea, FLENI, Buenos Aires, Argentina.
Department of Neurology, Marcial Quiroga Hospital, San Juan, Argentina.
Mult Scler Relat Disord. 2017 Jul;15:42-46. doi: 10.1016/j.msard.2017.04.007. Epub 2017 May 3.
Susac Syndrome is an autoimmune endotheliopathy affecting capillaries and precapillary arterioles of the brain, inner ear and retina. The classic symptom triad includes visual disturbances, hypoacusia, and encephalopathy, but is rarely fully manifest at onset. The syndrome typically follows an active fluctuating monophasic course. Typical imaging findings on brain magnetic resonance show central fiber microischemias/microinfarctions of the corpus callosum known as "snow balls", as well as lineal infarcts and upper callosal fiber involvement. Fluorescein angiography and tonal audiometry are important tools to confirm diagnosis, even in patients who are asymptomatic for visual or auditory disturbances. We describe 8 patients with Susac Syndrome treated at our center and compare findings to those of other published case series.
Eight adults with Susac Syndrome diagnosed between January 2007 and August 2016 at our center, in Buenos Aires, Argentina are described. Magnetic Brain Resonance, fluorescein angiography, tonal audiometry, a complete serologic battery and lumbar puncture were performed to all patients.
The majority of patients were males, and average age at diagnosis was 37.5 years (range: 22-52 yrs). Two patients presented full clinical triad at onset, while the remaining developed visual and/or auditory disturbances later during the course of disease. All cases manifested varied neurological symptoms including pyramidal and/or sensory tract symptoms, amnesic disorders, ataxia and vertigo. Psychiatric manifestations such as disinhibition, aggressive behavior, paranoid ideation and hallucinations were also present. Seven patients suffered at least one relapse. Typical central corpus callosum fiber ischemias/infarcts, also known as snowball lesions were visible in all patients. Spokes, icicles, periventricular lesions and internal capsule "string of beads" patterns were observed on diffusion weighted images. Four cases presented fornix microischemias/microinfarctions, 5 juxtacortical involvement and 3 infratentorial infarcts. Leptomeningeal involvement was evident in only 1 patient after rabies vaccination. Fluorescein angiography was abnormal in 7 cases. Tonal audiometry revealed unilateral hypoacusia in 5 patients, 3 with low frequency hearing loss. Immunosuppressive treatment was indicated in all cases. Patient follow up ranged between 6 months and 9 years, only 1 patient was lost to follow up after three years.
Susac Syndrome is probably both underdiagnosed and misdiagnosed. Early and aggressive immunosuppressive treatment is indicated in order to prevent potential disabilities.
Susac综合征是一种自身免疫性内皮病,可影响脑、内耳和视网膜的毛细血管及毛细血管前小动脉。典型的症状三联征包括视觉障碍、听力减退和脑病,但在发病时很少完全显现。该综合征通常呈活动性波动的单相病程。脑部磁共振成像的典型表现为胼胝体中央纤维微缺血/微梗死,即所谓的“雪球”,以及线性梗死和胼胝体上部纤维受累。荧光素血管造影和纯音听力测定是确诊的重要手段,即使对于无视觉或听觉障碍症状的患者也是如此。我们描述了在我们中心接受治疗的8例Susac综合征患者,并将结果与其他已发表的病例系列进行比较。
描述了2007年1月至2016年8月在阿根廷布宜诺斯艾利斯我们中心诊断的8例成年Susac综合征患者。对所有患者均进行了脑部磁共振成像、荧光素血管造影、纯音听力测定、全套血清学检查和腰椎穿刺。
大多数患者为男性,诊断时的平均年龄为37.5岁(范围:22 - 52岁)。2例患者在发病时出现了完整的临床三联征,其余患者在病程后期出现了视觉和/或听觉障碍。所有病例均表现出各种神经系统症状,包括锥体束和/或感觉束症状、失忆障碍、共济失调和眩晕。还存在精神症状,如脱抑制、攻击行为、偏执观念和幻觉。7例患者至少复发一次。所有患者均可见典型的胼胝体中央纤维缺血/梗死,即雪球样病变。在扩散加权图像上观察到辐条样、冰柱样、脑室周围病变和内囊“串珠”样模式。4例患者出现穹窿微缺血/微梗死,5例患者出现皮质下受累,3例患者出现幕下梗死。仅1例患者在接种狂犬病疫苗后出现软脑膜受累。7例患者荧光素血管造影异常。纯音听力测定显示5例患者单侧听力减退,3例为低频听力损失。所有病例均给予免疫抑制治疗。患者随访时间为6个月至9年,仅1例患者在3年后失访。
Susac综合征可能存在诊断不足和误诊的情况。为预防潜在残疾,需尽早积极进行免疫抑制治疗。