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超声检查方案如何改善巨细胞动脉炎脑血管并发症的及时诊断。

How the ultrasound protocol may improve the timely diagnosis of cerebrovascular complications in giant cell arteritis.

作者信息

Maranini Beatrice, Pugliatti Maura, Govoni Marcello

机构信息

Rheumatology Unit, Department of Medical Sciences, University of Ferrara, Azienda Ospedaliero- Universitaria, Ferrara.

Unit of Neurology, Department of Neurosciences and Rehabilitation, University of Ferrara, Azienda Ospedaliero-Universitaria, Ferrara.

出版信息

Reumatismo. 2025 Jul 8. doi: 10.4081/reumatismo.2025.1831.

DOI:10.4081/reumatismo.2025.1831
PMID:40631891
Abstract

Giant cell arteritis (GCA) is a granulomatous inflammatory vasculitis of medium and large vessels, with a predilection for the external carotid and ophthalmic arteries and, to a lesser extent, for the vertebral arteries. In early phases of the disease, symptoms may be nonspecific, such as malaise, fever, and weight loss. Overt typical GCA symptoms are temporal headache, scalp tenderness, jaw claudication, and sudden vision loss. Inflammatory vessel involvement in GCA results in partial or complete occlusion of the arterial lumen, leading to complications such as acute ischemic optic neuropathy, transient ischemic attack, and ischemic stroke. The latter is a rare but severe complication of GCA, and it has been reported in 2.8-7% of patients diagnosed with GCA. The majority of ischemic strokes are related to inflammation of vertebral and, less frequently, basilar and internal carotid arteries. Stroke in GCA patients affects vertebrobasilar circulation in 50 to 100% of cases, compared to only 20% observed in cerebrovascular accidents in the general population. Prompt diagnosis of GCA cranial involvement is pivotal, since early start of high-dose corticosteroid treatment and/or immunosuppressive drugs (e.g., tocilizumab and methotrexate) is highly effective in preventing further evolution and recurrence of such complications. In this viewpoint, we have briefly pinpointed the current possible value of vertebral ultrasound from both the rheumatologist's and neurologist's point of view.

摘要

巨细胞动脉炎(GCA)是一种累及中、大动脉的肉芽肿性炎症性血管炎,好发于颈外动脉和眼动脉,较少累及椎动脉。在疾病早期,症状可能不具特异性,如不适、发热和体重减轻。典型的GCA明显症状有颞部头痛、头皮压痛、颌部间歇性运动障碍和突然失明。GCA中炎症性血管受累会导致动脉管腔部分或完全闭塞,从而引发急性缺血性视神经病变、短暂性脑缺血发作和缺血性中风等并发症。后者是GCA一种罕见但严重的并发症,在确诊为GCA的患者中发生率为2.8%-7%。大多数缺血性中风与椎动脉炎症有关,较少与基底动脉和颈内动脉炎症有关。GCA患者中风在50%至100%的病例中影响椎基底循环,而在普通人群的脑血管意外中这一比例仅为20%。及时诊断GCA累及颅脑至关重要,因为早期开始高剂量皮质类固醇治疗和/或免疫抑制药物(如托珠单抗和甲氨蝶呤)在预防此类并发症的进一步发展和复发方面非常有效。从这个角度出发,我们从风湿病学家和神经科医生的角度简要指出了目前椎动脉超声检查可能具有的价值。

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