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双侧颈内动脉节段性缺如伴海绵体丛代偿及基底动脉缺如:病例报告

Bilateral segmental absence of the internal carotid artery with rete compensation associated with absence of basilar artery: case report.

作者信息

Kim Myoung Soo, Lee Seung-Joon, Lee Chae Heuck, Park Hyo Il

机构信息

Department of Neurosurgery, Seoul Paik Hospital, Inje University College of Medicine, Seoul 100-032, South Korea.

出版信息

Surg Neurol. 2006 Jun;65(6):615-9; discussion 619; author reply 620. doi: 10.1016/j.surneu.2005.07.072.

DOI:10.1016/j.surneu.2005.07.072
PMID:16720187
Abstract

BACKGROUND

Bilateral ICA absence is a rare lesion. Collateral circulation to the middle and anterior cerebral arteries in the absence of one or both ICAs may develop transcranial anastomoses from the external carotid system, a so-called CRM. Very rarely, theses arterial channels are observed in humans.

CASE DESCRIPTION

In the following case study, a 38-year-old man presented himself. He had a headache and scalp laceration after having had an accident. A right external carotid angiography identified anastomoses to distal intracranial vessel through the internal maxillary artery, but the intracranial vessels were only faintly visible. A right ascending pharyngeal arteriography showed an abnormal course and anastomoses with the intracranial vessel. The right ICA was absent. The left external carotid angiography demonstrated a network of tortous arteries in the region of the cavernous and petrous portion of ICA. The plexus of vessels on the left side communicated with the proximal part of the cavernous segment of the ICA. Both vertebral angiographies demonstrated a sudden diminution in caliber at the level of vertebrobasilar junction. There was an anomalous arterial collateral circulation originating from vertebral muscular and meningeal branch. There was also an absence of the basilar artery (BA).

CONCLUSION

This is the first case with CRM associated with bilateral segmental ICA and BA absence. The cause of this bilateral segmental ICA and BA absence may be maldevelopment of vessel connective tissue or extracellular matrix.

摘要

背景

双侧颈内动脉缺如是一种罕见的病变。在一侧或双侧颈内动脉缺如的情况下,大脑中动脉和前动脉的侧支循环可能通过颈外动脉系统形成经颅吻合,即所谓的颈动脉-海绵窦瘘(CRM)。在人类中很少观察到这些动脉通道。

病例描述

在以下病例研究中,一名38岁男性前来就诊。他在发生事故后出现头痛和头皮裂伤。右侧颈外动脉血管造影显示通过上颌内动脉与颅内远端血管存在吻合,但颅内血管仅隐约可见。右侧咽升动脉血管造影显示走行异常并与颅内血管存在吻合。右侧颈内动脉缺如。左侧颈外动脉血管造影显示在颈内动脉海绵窦段和岩骨段区域有一个迂曲动脉网络。左侧血管丛与颈内动脉海绵窦段近端相通。双侧椎动脉血管造影均显示在椎基底动脉交界处水平管径突然变细。存在源自椎动脉肌支和脑膜支的异常动脉侧支循环。基底动脉(BA)也缺如。

结论

这是首例与双侧节段性颈内动脉和基底动脉缺如相关的颈动脉-海绵窦瘘病例。这种双侧节段性颈内动脉和基底动脉缺如的原因可能是血管结缔组织或细胞外基质发育异常。

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