Department of Pediatrics, Division of Pediatric Neurology, Ankara City Hospital, Children's' Hospital, Ankara, Turkey.
Department of Pediatrics, Division of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara, Turkey.
Mult Scler Relat Disord. 2023 Nov;79:104948. doi: 10.1016/j.msard.2023.104948. Epub 2023 Aug 26.
To evaluate clinical characteristics, imaging features and etiological profile of Radiologically Isolated Syndrome (RIS) along with clinical and radiological follow-up.
Demographic, clinical and radiological data of patients younger than 18 years fulfilling the criteria for RIS were retrospectively analyzed. RIS was defined by the detection of lesions meeting the revised 2010 McDonald Criteria for dissemination in space on magnetic resonance imaging (MRI) in the absence of any symptoms of demyelinating disease or an alternative cause for the MRI findings.
There were total 69 patients (38 girls, 31 boys). The median age at index MRI was 15.7 years, and median follow-up time was 28 months. The most common reason for neuroimaging was headache (60.9%). A first clinical event occurred with median 11 months in 14/69 (20%) of cases. Those with oligoclonal bands (OCB) in cerebrospinal fluid (CSF) and follow-up longer than 3 years were more likely to experience a clinical event (p<0.05): 25% of those with OCB manifested clinical symptoms within the first year and 33.3% within the first two years compared to 6.3% and 9.4%, respectively in those without OCB. Radiological evolution was not associated with any variables: age, sex, reason for neuroimaging, serum 25-hydroxyvitamin D level, elevated IgG index, OCB positivity, total number and localization of lesions, presence of gadolinium enhancement, achievement of 2005 criteria for DIS and duration of follow-up.
Children and adolescents with RIS and CSF OCB should be followed-up for at least 3 years in order to detect any clinical symptoms suggestive of a demyelinating event. Because disease-modifying treatments are not approved in RIS and no consensus report justifies their use especially in pediatric RIS, close follow-up of OCB-positive patients is needed for early recognition of any clinical event and timely initiation of specific treatment.
评估放射孤立综合征(RIS)的临床特征、影像学特征和病因谱,并进行临床和影像学随访。
回顾性分析符合 RIS 诊断标准且年龄小于 18 岁的患者的人口统计学、临床和影像学数据。RIS 定义为磁共振成像(MRI)上发现符合修订后的 2010 年 McDonald 空间分布扩展标准的病灶,但无脱髓鞘疾病的任何症状或 MRI 发现的其他原因。
共有 69 例患者(38 名女孩,31 名男孩)。首诊 MRI 时的中位年龄为 15.7 岁,中位随访时间为 28 个月。最常见的神经影像学检查原因是头痛(60.9%)。14/69(20%)例患者首发临床事件的中位时间为 11 个月。脑脊液寡克隆带(OCB)阳性和随访时间超过 3 年的患者更有可能发生临床事件(p<0.05):OCB 阳性患者中有 25%在第一年出现临床症状,33.3%在第二年出现症状,而 OCB 阴性患者中分别为 6.3%和 9.4%。影像学演变与任何变量均无相关性:年龄、性别、神经影像学检查原因、血清 25-羟维生素 D 水平、升高的 IgG 指数、OCB 阳性、病灶总数和定位、钆增强的存在、达到 2005 年 DIS 标准和随访时间。
具有 RIS 和 CSF OCB 的儿童和青少年应至少随访 3 年,以检测任何提示脱髓鞘事件的临床症状。由于疾病修正治疗在 RIS 中未获批准,且没有共识报告证明其在儿科 RIS 中的使用合理性,因此需要对 OCB 阳性患者进行密切随访,以早期发现任何临床事件并及时开始特定治疗。