单侧原发性颈动脉炎1例报告

Luigi Francesco Saccaro, Beatrice A. Milano, S. Galletta
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摘要

我们报告了第一例孤立性单侧颈动脉炎,发生在一名没有其他疾病的患者的上呼吸道感染之后。我们收集了患者住院和随访期间的临床信息。通过Pubmed搜索,我们发现了讨论TIPIC综合征、颈动脉疼痛或炎症的文章。在审查了这些文章和相应的图像后,这些文章都没有报告与我们相似的临床和放射学发现。一名55岁的男性因单侧颈部疼痛接受咨询,除了上呼吸道感染外,没有相关临床病史,也没有其他体征或症状。入院前的核磁共振成像显示左颈内动脉局灶性外膜炎症的迹象。超声在左颈内动脉起始处发现一个具有低回声和等回声成分的混合斑块。特别是,没有任何晕征提示巨细胞动脉炎。广泛的实验室检查只发现血浆IL-1受体拮抗剂增加。在皮质类固醇和乙酰水杨酸治疗三天后。,颈痛完全消退,泼尼松停止使用。患者于第7天出院,每天服用乙酰水杨酸。三个月时,他仍然没有症状,颈动脉超声与第一次相当,并停止了治疗。我们认为,考虑到颈动脉壁的局灶性、孤立性受累,颈动脉的单纯血管炎症可以适当地定义为“颈动脉炎”,而且这种单侧表现以前从未报道过。推测性地,我们提出了胡萝卜素与该患者上呼吸道感染之间的联系。
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Unilateral Primary Carotiditis: A Case Report
We report the first case of isolated unilateral carotid arteritis, following an upper respiratory tract infection in a patient without other medical conditions. We collected clinical information during the patient’s hospitalization and follow-up. Through a Pubmed search, we identified articles discussing TIPIC syndrome, carotid pain, or inflammation. After reviewing the articles and the corresponding images, none of these reported clinical and radiological findings similar to ours. A 55-year-old man consulted for unilateral neck pain, without relevant clinical history apart from an upper respiratory tract infection, nor other signs or symptoms. An MRI before admission showed signs of focal adventitial inflammation of the left internal carotid artery. Ultrasound identified a mixed plaque with hypoechoic and isoechoic components at the beginning of the left internal carotid. In particular, there was no halo sign suggestive of giant cell arteritis. Extensive laboratory exams only found increased plasma IL-1 receptor antagonist. After three days of corticosteroid and acetylsalicylic acid treatment., cervicalgia completely regressed, and prednisone was stopped. The patient was discharged on day 7 on daily acetylsalicylic acid. At three months, he remained asymptomatic, carotid ultrasound was comparable to the first one, and treatment was stopped. We suggest that a purely vascular inflammation of the carotid could appropriately be defined “carotiditis”, considering the focal, isolated involvement of the carotid wall, and that such a unilateral presentation has never been reported before. Speculatively, we propose an association between carotidis and the upper respiratory tract infection in this patient.
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