Hou Dianbin, Mei Yu, Ji Yongqiang, Wu Hongliang, Zhang Huilong, Sun Zhongwen, Li Wenjuan, Li Bing, Ren Chao, Guan Lina, Liu Chuanyu
Department of Neurology.
Department of Nephrology.
Medicine (Baltimore). 2019 Jan;98(1):e13986. doi: 10.1097/MD.0000000000013986.
Congenital internal carotid artery hypoplasia (CICAH) is rarely reported. This study aimed to discuss the epidemiological characteristics, clinical manifestation, imaging and treatment of CICAH.
The case was male who showed barylalia and limited abilities of the left limbs as their main clinical manifestation. This patient was diagnosed CICAH by digital subtraction angiography (DSA) and computed tomography (CT).
CICAH.
The patient underwent anti platelet aggregation, lipid-lowering, improving cerebral circulation.
The patient was in a stable condition after management of cerebrovascular risk.
Given the asymptomatic and congenital nature of carotid agenesis, no treatment is necessary or possible to re-establish the internal carotid artery (ICA). However, with the high risk of aneurysm and cerebrovascular insufficiency, management of cerebrovascular risk is important. Urgent radiological assessment is necessary for patients with suspicious neurological symptoms.
先天性颈内动脉发育不全(CICAH)鲜有报道。本研究旨在探讨CICAH的流行病学特征、临床表现、影像学表现及治疗方法。
该病例为男性,主要临床表现为言语不清和左肢活动能力受限。该患者通过数字减影血管造影(DSA)和计算机断层扫描(CT)被诊断为CICAH。
CICAH。
患者接受了抗血小板聚集、降脂、改善脑循环治疗。
经过脑血管风险管理后,患者病情稳定。
鉴于颈动脉发育不全的无症状性和先天性,无需也无法进行治疗以重建颈内动脉(ICA)。然而,由于动脉瘤和脑血管供血不足的风险较高,脑血管风险的管理很重要。对于有可疑神经症状的患者,紧急进行放射学评估是必要的。