颈内动脉重复伴同侧持久镫骨动脉及对侧异常颈内动脉1例。

Journal of neuroendovascular therapy Pub Date : 2025-01-01 Epub Date: 2024-12-25 DOI:10.5797/jnet.cr.2024-0091
Hidetaka Hayashi, Hiro Kiyosue, Yoshitaka Tamura, Mari Yonemura, Sachiko Uchiumi, Yuika Watanabe, Aya Kanemitsu, Hiroyuki Uetani, Seitaro Oda, Toshinori Hirai
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引用次数: 0

摘要

目的:颅外脑动脉重复是一种罕见的解剖变异,最常见于椎动脉。然而,颈内动脉(ICA)的重复是极其罕见的。我们提出了一个独特的病例,患者诊断为右侧面动脉瘤,其中右侧重复的ICA,同侧持续性镫骨动脉(PSA),和对侧异常的ICA偶然发现。病例介绍:一名56岁女性,右下颚无痛性肿块。体格检查发现一个圆形搏动肿块。增强CT显示一25毫米囊状动脉瘤起源于右侧面动脉,同时伴有右侧重复的ICA和左侧异常的ICA。右侧重复ICA外侧肢和左侧异常ICA外侧肢穿过鼓室进入颈动脉管。右棘孔的缺失表明PSA的存在。血管造影证实了重复的ICA,异常的ICA和PSA。右侧重复ICA的侧肢产生枕骨动脉和一个小分支,PSA,进入中颅窝。成功栓塞面动脉瘤。后续MR血管造影显示动脉瘤稳定闭塞,重复的ICA同时发出来自外侧肢体的PSA和来自内侧肢体的咽支。结论:本病例为胎儿时期宫颈动脉系统的发育提供了有价值的见解,特别是连接第三弓和背主动脉的侧支通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Duplicated Cervical Internal Carotid Artery with Ipsilateral Persistent Stapedial Artery and Contralateral Aberrant Internal Carotid Artery: A Case Report.

Objective: Duplication of extracranial cerebral arteries is a rare anatomical variant, most commonly observed in the vertebral artery. However, duplication of the cervical internal carotid artery (ICA) is extremely rare. We present a unique case of a patient diagnosed with a right facial artery aneurysm, in whom a right duplicated ICA, ipsilateral persistent stapedial artery (PSA), and contralateral aberrant ICA were incidentally identified.

Case presentation: A 56-year-old woman presented with a painless mass in the right lower jaw. Physical examination revealed a round, pulsatile mass. Contrast-enhanced CT demonstrated a 25 mm saccular aneurysm originating from the right facial artery, along with a right duplicated ICA and a left aberrant ICA. The lateral limb of the right duplicated ICA and the left aberrant ICA were seen traversing the tympanic cavity and entering the carotid canal. The absence of the right foramen spinosum indicated the presence of a PSA. Angiography confirmed the duplicated ICA, aberrant ICA, and PSA. The lateral limb of the right duplicated ICA gave rise to the occipital artery and a small branch, the PSA, which entered the middle cranial fossa. The facial artery aneurysm was successfully embolized. Follow-up MR angiography showed stable occlusion of the aneurysm, with the duplicated ICA giving off both the PSA from the lateral limb and a pharyngeal branch from the medial limb.

Conclusion: This case provides valuable insights into the development of the cervical arterial system during the fetal period, particularly the collateral pathways connecting the third arch to the dorsal aorta.

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