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双侧颈内动脉发育不全:一例病例研究及文献综述

Bilateral internal carotid artery agenesis: a case study and review of the literature.

作者信息

Cali R L, Berg R, Rama K

机构信息

FACS, Detroit, MI 48236.

出版信息

Surgery. 1993 Feb;113(2):227-33.

PMID:8430372
Abstract

Bilateral internal carotid artery agenesis is a rare lesion, with only 18 cases previously reported. Blood supply to the anterior cerebral circulation is most commonly through enlarged basilar and posterior communicating arteries. Occasionally collateral flow is through abnormal transsellar anastomoses or anastomoses between the external carotid and intracranial systems. Associated intracranial aneurysms occur in 25% of patients, accounting for a significant incidence of intracranial hemorrhage as the initial symptom. Diagnosis is best made by cerebral arteriography with computed tomography to verify the congenital nature of the abnormality by demonstrating the absence of carotid canals. This is the second case to begin with transient ischemic attacks suggestive of carotid territory ischemia but originating from the vertebral system. Angiographic findings included absent internal carotid arteries, small common carotid arteries, and bilateral high-grade stenoses at the origins of large vertebral arteries. This is the first such case to be treated with reimplantation of the vertebral artery with resolution of symptoms.

摘要

双侧颈内动脉缺如是一种罕见的病变,此前仅报道过18例。大脑前循环的血液供应最常见的是通过扩大的基底动脉和后交通动脉。偶尔,侧支血流通过异常的经蝶窦吻合或颈外动脉与颅内系统之间的吻合。25%的患者会出现相关的颅内动脉瘤,这是颅内出血作为首发症状的显著发生率。诊断最好通过脑动脉造影和计算机断层扫描来进行,通过显示颈动脉管的缺失来证实异常的先天性本质。这是第二例以短暂性脑缺血发作开始的病例,提示颈动脉区域缺血,但起源于椎体系。血管造影结果包括颈内动脉缺如、颈总动脉细小以及双侧椎动脉起始处高度狭窄。这是首例通过椎动脉再植术治疗且症状缓解的此类病例。

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