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原发性中枢神经系统血管炎——诊断、鉴别诊断及治疗的最新进展

Primary central nervous system vasculitis - An update on diagnosis, differential diagnosis and treatment.

作者信息

Kraemer Markus, Berlit Peter

机构信息

Department of Neurology, Alfried Krupp Hospital, Alfried-Krupp-Strasse 21, 45130 Essen, Germany; Department of Neurology, Medical Faculty, Heinrich Heine University, Moorenstrasse 5, 40225 Düsseldorf, Germany.

Department of Neurology, Alfried Krupp Hospital, Alfried-Krupp-Strasse 21, 45130 Essen, Germany; German Society of Neurology, Reinhardtstrasse 27 C, 10117 Berlin, Germany.

出版信息

J Neurol Sci. 2021 May 15;424:117422. doi: 10.1016/j.jns.2021.117422. Epub 2021 Mar 27.

Abstract

IMPORTANCE

Primary angiitis of the central nervous system (PACNS) is a rare condition which is often misdiagnosed. In order to avoid mistakes in the management, a step by step approach is necessary.

OBSERVATIONS

The most common presenting symptoms of PACNS are encephalopathy-related cognitive and affective abnormalities, headaches and multifocal symptoms associated with recurrent episodes of ischemia or hemorrhage. Seizures and spinal cord lesions may also occur. Diagnostic work up includes MRI, CSF examination, angiography and brain biopsy. Since all reported signs and findings lack specificity, the exclusion of differential diagnoses is essential before immunosuppressive therapy is started. Important differential diagnoses include reversible cerebral vasoconstriction syndrome, cerebral involvement of systemic vasculitides or rheumatic diseases, moyamoya angiopathy and infectious vasculopathies Effective treatment has been reported with glucocorticoids in combination with cyclophosphamide or rituximab; however, randomized clinical trials of PACNS treatment do not exist.

CONCLUSIONS AND RELEVANCE

PACNS is an important but rare differential diagnosis in daily neurological practice. The strict adherence to diagnostic criteria and the avoidance of inappropriate therapies in non-inflammatory vasculopathies and infectious diseases are essential.

摘要

重要性

中枢神经系统原发性血管炎(PACNS)是一种罕见疾病,常被误诊。为避免治疗失误,采取逐步诊断方法很有必要。

观察结果

PACNS最常见的症状是与脑病相关的认知和情感异常、头痛以及与缺血或出血反复发作相关的多灶性症状。也可能出现癫痫发作和脊髓病变。诊断检查包括磁共振成像(MRI)、脑脊液检查、血管造影和脑活检。由于所有报告的体征和发现都缺乏特异性,在开始免疫抑制治疗前排除鉴别诊断至关重要。重要的鉴别诊断包括可逆性脑血管收缩综合征、系统性血管炎或风湿性疾病的脑部受累、烟雾病和感染性血管病。已有报道使用糖皮质激素联合环磷酰胺或利妥昔单抗进行有效治疗;然而,尚无PACNS治疗的随机临床试验。

结论与意义

PACNS在日常神经科实践中是一个重要但罕见的鉴别诊断。严格遵循诊断标准并避免在非炎性血管病和传染病中进行不恰当治疗至关重要。

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