摘要
Abstract
Primary angiitis of the central nervous system(PACNS)is a rare immune-inflammatory disease confined to the small and medium blood vessels of the central nervous system,with unclear etiology and pathogenesis.The inci-dence of PACNS in the general population has not been accurately defined,and its clinical management is challenged by diagnostic difficulty,a high recurrence rate,and limited evidence supporting therapeutic interventions.The disease pre-dominantly occurs in people aged 40-60 years,with headache,cognitive impairment,and neurological deficits as the main clinical manifestations,which are non-specific.There are no characteristic indicators in laboratory tests,and cerebrospinal fluid examination can only rule out infection.Imaging findings include multiple infarctions and segmental vascular steno-sis.Brain tissue biopsy is the gold standard for diagnosis.Clinically,the Calabrese and Mallek diagnostic criteria are of-ten used,combined with supplementary criteria for stratified diagnosis.Treatment is based on glucocorticoids,with strati-fied induction,maintenance,and intensive therapy according to the type of involved blood vessels and disease severity,combined with immunosuppressants such as cyclophosphamide and mycophenolate mofetil.Biologics may be considered for refractory or recurrent cases.Long-term immunosuppressive therapy may reduce the risk of recurrence.Antiplatelet drugs,thrombolysis,and endovascular therapy can be used as needed.Currently,the diagnosis and treatment of PACNS still rely on diagnosis of exclusion and expert consensus,lacking high-level evidence.Future efforts should focus on exploring specific diagnostic markers and precise treatment regimens to promote standardized diagnosis and treatment.关键词
原发性中枢神经系统血管炎/免疫炎症/循证医学Key words
Primary angiitis of the central nervous system/Immune inflammation/Evidence-based medicine分类
医药卫生
