Ding Yun-Long, Niu Jia-Li, Ma Li, Gu Zhi-Qun, Zhai Ting-Ting, Liu Yan
Department of Neurology.
Department of Clinical Pharmacy, Jingjiang People's Hospital, the Seventh Affiliated Hospital of Yangzhou University, Jiangsu.
Medicine (Baltimore). 2019 Nov;98(44):e17779. doi: 10.1097/MD.0000000000017779.
Absence or hypoplasia of the internal carotid artery (ICA) are rare developmental anomalies. Usually, patients with ICA agenesis are asymptomatic due to collateral circulation, but they may present with seizures, headache, or transient ischemic attack. We report a patient with right ICA absence in whom "paroxysmal right eye amaurosis" was the main symptom.
A 76-year-old male patient suffered from "paroxysmal right eye amaurosis for 3 years". Three years prior, the patient had suffered sudden one-minute right eye amaurosis without any obvious cause. The attack reoccurred 1-2 times/year until one week before admission when he experienced two sudden right eye amaurosis.
Congenital absence of the right ICA was diagnosed. In this patient with congenital absence of the right ICA, the ipsilateral anterior cerebral artery (ACA) was compensated by the anterior communicating artery (ACOM), and the ipsilateral middle cerebral artery (MCA) emerged from the carotid siphon of the contralateral ICA.
The patient was given antiplatelet treatment consisting of aspirin and atorvastatin after admission and instructed to maintain the treatment after discharge.
No symptom onset was observed during follow-up.
Here, we report the patient's clinical manifestations and imaging findings and analyze the cause of the condition to provide a clinical reference for the study of congenital absence of the ICA.
颈内动脉(ICA)缺如或发育不全是罕见的发育异常。通常,ICA发育不全的患者由于侧支循环而无症状,但可能出现癫痫发作、头痛或短暂性脑缺血发作。我们报告了一名以“阵发性右眼黑矇”为主要症状的右侧ICA缺如患者。
一名76岁男性患者患有“阵发性右眼黑矇3年”。3年前,患者无明显诱因突然出现右眼黑矇1分钟。发作每年复发1 - 2次,直到入院前一周,他又经历了两次突然的右眼黑矇。
诊断为先天性右侧ICA缺如。在这名先天性右侧ICA缺如的患者中,同侧大脑前动脉(ACA)由前交通动脉(ACOM)代偿,同侧大脑中动脉(MCA)起源于对侧ICA的颈动脉虹吸部。
患者入院后给予阿司匹林和阿托伐他汀抗血小板治疗,并在出院后指导其维持治疗。
随访期间未观察到症状发作。
在此,我们报告患者的临床表现和影像学检查结果,并分析病情原因,为先天性ICA缺如的研究提供临床参考。