Ruptured aneurysm originating from an infundibular dilatation of the posterior communicating artery associated with a hyperplastic anterior choroidal artery: A case report

IF 0.4 Q4 CLINICAL NEUROLOGY
Ryota Kimura , Ichiro Nakagawa , Hisashi Kawai , Yoshinari Okumura
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引用次数: 0

Abstract

Background

A hyperplastic anterior choroidal artery (AChA) resulting from incomplete distal annexation between the primitive AChoA and the posterior cerebral artery, increases the risk of cerebral aneurysms at the branching site of the AChA and other distant locations. It has also been reported that infundibular dilatation (IFD) rarely progresses into a saccular aneurysm with a risk of rupture.

Case report

A 59-year-old man presented with sudden onset of headache and vomiting due to the rupture of an aneurysm originating from an IFD of the posterior communicating artery (PcomA) associated with a hyperplastic AChA. The aneurysm was successfully treated using coil embolization.

Conclusion

To the best of our knowledge, this is the first reported case of a ruptured aneurysm originating from an IFD of the PcomA associated with a hyperplastic AChA, accompanied by a review of previous case reports. Neurosurgeons should be aware of this anomaly to prevent critical events.

后交通动脉扩张引起的动脉瘤破裂伴前脉络膜动脉增生1例
原始脉络膜前动脉与大脑后动脉之间远端不完全合并导致的脉络膜前动脉(AChA)增生,增加了AChA分支部位和其他远处部位发生脑动脉瘤的风险。也有报道称,漏斗扩张(IFD)很少发展为囊状动脉瘤,并有破裂的风险。病例报告:一名59岁男性患者因后交通动脉IFD (PcomA)动脉瘤破裂并伴有增生性AChA而突然出现头痛和呕吐。动脉瘤采用线圈栓塞成功治疗。结论:据我们所知,这是第一例由PcomA的IFD引起的动脉瘤破裂并伴有增生性AChA的病例,并对以往的病例报告进行了回顾。神经外科医生应该意识到这种异常,以防止严重事件的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
236
审稿时长
15 weeks
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