海绵内颈内动脉重复。

Q3 Medicine Acta neurologica Taiwanica Pub Date : 2019-06-15
Giacomo Rebella, Antonio Castaldi, Umberto G Rossi
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引用次数: 0

摘要

情况下。除药理学控制的轻度高血压外,无明显既往病史。在神经学检查中,患者表现出警觉,定向,没有力量,敏感性和协调性的缺陷。证实为表现性暂时性失语,怀疑为短暂性脑缺血发作(TIA)。颅脑ct血管造影(CTA)显示左侧颈内动脉(ICA)发育不全,海绵内段出现局灶性重复(图1,箭头)。威利斯圈呈规则状,左侧大脑中动脉由椎基底动脉系统通过口径增大的左侧后交通动脉支持,并由对侧ICA通过前交通动脉支持。因此,患者接受了数字减影血管造影(DSA)侧位视图,证实了左侧海绵内ICA的节段性重复(图2,箭头)。血管在海绵窦内有轻微的弯曲,其汇合处下游的颅内分支在视觉上有轻微的延迟。几小时后,她的症状完全消退,与临床和影像学资料一致,诊断为TIA。事实上,短暂性脑缺血事件很可能是由于ICA发育不全和上述海绵管内束异常导致颅内血流分布的改变和减少,导致左脑半球血流减少所致。患者开始抗血小板药物治疗,出院后进行临床、实验室和影像学随访。颅内束ICA的重复是非常罕见的(1,2)。大多数病例局限于腰线上段。据我们所知,这是文献中描述的第一例海绵管内ICA的真正重复。先天性变异或获得性病理的ICA患者大多无症状,但当症状出现时,必须对患者进行检查(1-3)。CTA被认为是颅内血管解剖的一线无创诊断方法。目前,对于颅内束无并发症重复ICA的患者,药物治疗仍是首选。
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Duplication of Intracavernous Internal Carotid Artery.

ation. No significant past medical history except for pharmacologically controlled mild hypertension. During the neurological examination the patient appeared alert, oriented and showed no deficit of strength, sensitivity and coordination. An expressive temporary aphasia was confirmed and Transient Ischemic Attacks (TIA) was suspected. Cranial Computed Tomography Angiography (CTA) showed hypoplasia of left Internal Carotid Artery (ICA) with a focal duplication in the intracavernous segment (Figure 1, arrowhead). Circle of Willis appears to be regular, with the left middle cerebral artery supported by the vertebrobasilar system through the left posterior communicating artery of increased caliber, and by the contralateral ICA via anterior communicating artery. Consequently, patient underwent Digital Subtraction Angiography (DSA) lateral view that confirmed the segmental duplication of the left intracavernous ICA (Figure 2, arrowhead). Vessels had a lightly winding course within the cavernous sinus and the intracranial branches downstream of their confluence presented a slight delay in visualization. After few hours her symptoms completely regressed and, in agreement with clinical and imaging data, diagnosis of TIA was made. The transient ischemic event was, in fact, most likely caused by low flow to the left cerebral hemisphere due to hypoplasia of the ICA and aforementioned abnormalities of its intracavernous tract that caused alteration and reduction of intracranial flow distribution. Medical treatment with anti-platelet drugs was started and patient was discharged with a clinical, laboratory and imaging follow-up program. Duplications of ICA in the intracranial tract are very rare(1,2). Most of the cases are localized in the supraclinoid segment. To our knowledge this is the first case described in literature of true duplication of ICA in the intracavernous tract. Patients with congenital variants or acquired pathology of ICA are mostly asymptomatic, but when symptoms appear, patients must be investigated(1-3). CTA is considered the first line non-invasive diagnostic method for intracranial vascular anatomy. At present, medical treatment remains the choice in patients with no-complicated duplications of ICA in the intracranial tract.

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来源期刊
Acta neurologica Taiwanica
Acta neurologica Taiwanica Medicine-Neurology (clinical)
CiteScore
1.30
自引率
0.00%
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0
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