Departments of1Radiology.
2Neurosurgery, and.
J Neurosurg. 2018 Jul;129(1):91-99. doi: 10.3171/2017.2.JNS1744. Epub 2017 Sep 29.
OBJECTIVE Over the last half century, there have been isolated case reports of purely arterial malformations. In this study, the authors report a consecutive series of patients with pure arterial malformations, emphasizing the clinical and radiological features of these lesions. METHODS Pure arterial malformations were defined as dilated, overlapping, and tortuous arteries with a coil-like appearance and/or a mass of arterial loops without any associated venous component. Demographic characteristics of the patients, cardiovascular risk factors, presentation, radiological characteristics, and follow-up data were collected. Primary outcomes were new neurological symptoms including disability, stroke, and hemorrhage. RESULTS Twelve patients meeting the criteria were identified. Ten patients were female (83.3%) and 2 were male (16.6%). Their mean age at diagnosis was 26.2 ± 11.6 years. The most common imaging indication was headache (7 patients [58.3%]). In 3 cases the pure arterial malformation involved the anterior cerebral arteries (25.0%); in 4 cases the posterior communicating artery/posterior cerebral artery (33.3%); in 2 cases the middle cerebral artery (16.6%); and in 1 case each, the superior cerebellar artery, basilar artery/anterior inferior cerebellar artery, and posterior inferior cerebellar artery. The mean maximum diameter of the malformations was 7.2 ± 5.0 mm (range 3-16 mm). Four lesions had focal aneurysms associated with the pure arterial malformation, and 5 were partially calcified. In no cases was there associated intracranial hemorrhage or infarction. One patient underwent treatment for the pure arterial malformation. All 12 patients had follow-up (mean 29 months, median 19 months), and there were no cases of disability, stroke, or hemorrhage. CONCLUSIONS Pure arterial malformations are rare lesions that are often detected incidentally and probably have a benign natural history. These lesions can affect any of the intracranial arteries and are likely best managed conservatively.
在过去的半个世纪中,已经有孤立的纯动脉畸形病例报告。在本研究中,作者报告了一系列连续的纯动脉畸形患者,强调了这些病变的临床和影像学特征。
纯动脉畸形定义为扩张、重叠、扭曲的动脉,呈线圈样外观和/或一团动脉环,无任何伴行静脉成分。收集患者的人口统计学特征、心血管危险因素、表现、影像学特征和随访数据。主要结局是新发神经症状,包括残疾、卒中和出血。
确定了符合标准的 12 名患者。10 名患者为女性(83.3%),2 名患者为男性(16.6%)。他们的诊断时平均年龄为 26.2±11.6 岁。最常见的影像学指征是头痛(7 例[58.3%])。3 例纯动脉畸形累及大脑前动脉(25.0%);4 例累及后交通动脉/大脑后动脉(33.3%);2 例累及大脑中动脉(16.6%);1 例分别累及小脑上动脉、基底动脉/小脑前下动脉和小脑后下动脉。畸形的最大直径平均值为 7.2±5.0mm(范围 3-16mm)。4 个病变与纯动脉畸形相关的局灶性动脉瘤,5 个部分钙化。无颅内出血或梗死。1 例患者接受了纯动脉畸形治疗。12 例患者均有随访(平均 29 个月,中位数 19 个月),无残疾、卒中和出血病例。
纯动脉畸形是罕见病变,通常是偶然发现的,可能具有良性自然史。这些病变可影响颅内任何动脉,可能最好保守治疗。