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复杂脑动脉异常:终末颈动脉和大脑中动脉呈网状形成伴双侧A1段开窗

Complex Cerebral Artery Anomaly Rete-like Formation of the Terminal Carotid and Middle Cerebral Arteries with Bilateral A1 Segments Fenestrations.

作者信息

Nestorovic Dragoslav, Nikolic Igor, Savic Andrija, Radanovic Drazen, Miletic Marko, Cvetic Vladimir

机构信息

Center for Radiology, University Clinical Centre of Serbia, Pasterova 2, 11000 Belgrade, Serbia.

Clinic for Neurosurgery, University Clinical Centre of Serbia, Koste Todorovica 4, 11000 Belgrade, Serbia.

出版信息

Diagnostics (Basel). 2025 May 26;15(11):1333. doi: 10.3390/diagnostics15111333.

Abstract

We present a rare case of a 16-year-old male who was admitted with bilateral tinnitus and subsequently underwent magnetic resonance imaging (MRI) and digital subtraction angiography (DSA) for further evaluation. The left internal carotid (ICA) artery had a normal caliber but ended as a stump at the C7 segment, with a network of filiform vessels from both the stump and right posterior communicating artery (PComm). The right PComm was hypertrophic and the right posterior cerebral artery (PCA) was mainly supplied by the right ICA. The right ICA's bifurcation and the initial middle cerebral artery (MCA) segment were absent, while the MCA trunk was hypoplastic. The right PCA and pial branches vascularized the temporal lobe, with collaterals between the PCA and MCA. The left ICA was slightly enlarged with double fenestration at the left A1 segment. The right A1 segment of the anterior cerebral artery had double fenestration and while several diagnoses were considered, no single diagnosis fully explained all clinical findings. A thorough review of the existing literature yielded no comparable cases, highlighting the uniqueness of this presentation. This case emphasizes the complexity of cerebral vascular anomalies and the challenges associated with diagnosing such rare conditions, underscoring the need for careful assessment.

摘要

我们报告一例罕见病例,一名16岁男性因双侧耳鸣入院,随后接受了磁共振成像(MRI)和数字减影血管造影(DSA)以进行进一步评估。左侧颈内动脉(ICA)管径正常,但在C7段以残端结束,残端和右侧后交通动脉(PComm)均有丝状血管网。右侧PComm增粗,右侧大脑后动脉(PCA)主要由右侧ICA供血。右侧ICA分叉及大脑中动脉(MCA)起始段缺如,而MCA主干发育不全。右侧PCA及其软膜分支为颞叶供血,PCA与MCA之间有侧支循环。左侧ICA在左侧A1段轻度增粗并伴有双孔。大脑前动脉右侧A1段有双孔,虽然考虑了多种诊断,但没有单一诊断能完全解释所有临床发现。对现有文献进行全面回顾未发现类似病例,突出了该病例表现的独特性。该病例强调了脑血管异常的复杂性以及诊断此类罕见疾病的挑战,凸显了仔细评估的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/12155128/a263793f2bef/diagnostics-15-01333-g001.jpg

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