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紧急状态国家中 Susac 综合征的特征和治疗:来自巴西的多中心病例系列。

Characteristics and management of Susac syndrome in an emergent country: a multi-center case series from Brazil.

机构信息

Neurology Service, Fortaleza General Hospital, Fortaleza, Brazil.

Division of Neurology, Department of Clinical Medicine, Federal University of Ceará, Rua Prof, Rodolfo Teófilo, Costa Mendes, 1608 - 4° andar, Fortaleza, , Ceará, Brazil.

出版信息

Neurol Sci. 2022 Nov;43(11):6449-6460. doi: 10.1007/s10072-022-06320-4. Epub 2022 Aug 9.

Abstract

BACKGROUND

Susac syndrome (SS) is a rare endotheliopathy with an estimated prevalence of 0.14-0.024 per 100,000. It is an important differential diagnosis in demyelinating disorders. There are few case series and no large randomized controlled trials, and most reports come from developed countries. We report six cases of SS in three centers in Brazil and discuss management challenges in emergent countries.

METHODS

This is a retrospective case series of patients diagnosed with SS in three medical centers in Brazil between April 2018 and July 2021. The European Susac consortium (EuSaC) criteria were used for diagnosis of SS. Demographic data and clinical interventions were described and outcomes were assessed subjectively and by applying the modified Rankin Scale (mRS) on last follow-up.

RESULTS

Six patients were diagnosed with SS (3 males, 3 females). Mean age at presentation was 36 years (range 17 to 54). The most common initial symptom was confusion, followed by visual impairment and hearing loss. Characteristic snowball lesions on magnetic resonance imaging (MRI) were present in four patients (66%). Retinal artery abnormalities were present in half (3/6) of patients, and sensorineural hearing loss was present in four patients (66%). Outcome was favorable (mRS ≤ 2) in five patients (86%). Patients treated early had a more favorable outcome.

CONCLUSION

Emergent countries face challenges in the diagnosis and management of patients with SS, such as access to advanced tests (fluorescein angiography, serial MRI) and treatment drugs (rituximab, mycophenolate). Further research should consider particularities of patients with SS in emergent countries.

摘要

背景

Susac 综合征(SS)是一种罕见的血管内皮病,估计发病率为每 10 万人中有 0.14-0.024 人。它是脱髓鞘疾病的重要鉴别诊断。目前仅有少数病例系列研究,且没有大型随机对照试验,大多数报告来自发达国家。我们报告了巴西三个中心的六例 SS 病例,并讨论了新兴国家的管理挑战。

方法

这是巴西三个医学中心 2018 年 4 月至 2021 年 7 月期间诊断为 SS 的患者的回顾性病例系列研究。采用欧洲 Susac 联合会(EuSaC)标准诊断 SS。描述了人口统计学数据和临床干预措施,并根据最后一次随访时的改良 Rankin 量表(mRS)进行了主观和客观评估。

结果

六例患者被诊断为 SS(3 例男性,3 例女性)。发病时的平均年龄为 36 岁(范围 17 至 54 岁)。最常见的首发症状是意识混乱,其次是视力障碍和听力损失。四名患者(66%)存在特征性的磁共振成像(MRI)雪球样病变。半数患者(3/6)存在视网膜动脉异常,四名患者(66%)存在感觉神经性听力损失。五例患者(86%)的预后良好(mRS≤2)。早期治疗的患者预后更好。

结论

新兴国家在 SS 患者的诊断和管理方面面临挑战,例如获得高级检查(荧光素血管造影、连续 MRI)和治疗药物(利妥昔单抗、霉酚酸酯)的机会有限。进一步的研究应考虑新兴国家 SS 患者的特殊性。

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