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Clinical and Imaging Characteristics of Diffuse Intracranial Dolichoectasia
W Brinjikji1,2, D M Nasr3, K D Flemming3
1From the Departments of Radiology (W.B., H.J.C., G.L., D.F.K.) brinjikji.waleed@mayo.edu.
Insights
Diffuse intracranial dolichoectasia, affecting multiple brain arteries, is a distinct condition with a worse prognosis than vertebrobasilar dolichoectasia. This phenotype is associated with systemic arteriopathy and higher aneurysm rupture rates.
Area of Science:
- Neurology
- Vascular Biology
- Medical Phenotyping
Background:
- Vertebrobasilar dolichoectasia (VBD) can coexist with anterior circulation disease.
- A subset of patients exhibits multivessel intracranial dolichoectasia, suggesting a distinct phenotype.
Purpose of the Study:
- To define and characterize diffuse intracranial dolichoectasia (DID).
- To compare clinical and angiographic features of DID with isolated VBD.
Main Methods:
- Retrospective review of patients with DID and VBD.
- Comparison of demographics, vascular risk factors, aneurysm prevalence, and outcomes.
- DID defined as aneurysmal dilation involving ≥2 intracranial vascular beds.
Main Results:
- Patients with DID were older and had higher rates of abdominal aortic aneurysms, visceral aneurysms, and smoking.
- DID was associated with increased aneurysm growth and rupture.
- Poorer neurological function and higher aneurysm-related death rates were observed in DID patients.
Conclusions:
- Diffuse intracranial dolichoectasia represents a distinct vascular phenotype.
- DID is linked to systemic arteriopathy and has a significantly worse natural history than VBD.
- Associated saccular and abdominal aortic aneurysms highlight a systemic vascular issue.
Background And Purpose:
Among patients with vertebrobasilar dolichoectasia is a subset of patients with disease affecting the anterior circulation as well. We hypothesized that multivessel intracranial dolichoectasia may represent a distinct phenotype from single-territory vertebrobasilar dolichoectasia. The purpose of this study was to characterize clinical characteristics and angiographic features of this proposed distinct phenotype termed "diffuse intracranial dolichoectasia" and compare them with those in patients with isolated vertebrobasilar dolichoectasia.
Materials And Methods:
We retrospectively reviewed a consecutive series of patients with diffuse intracranial dolichoectasia and compared their demographics, vascular risk factors, additional aneurysm prevalence, and clinical outcomes with a group of patients with vertebrobasilar dolichoectasia. "Diffuse intracranial dolichoectasia" was defined as aneurysmal dilation of entire vascular segments involving ≥2 intracranial vascular beds. Categoric and continuous variables were compared by using χ2 and Student t tests, respectively.
Results:
Twenty-five patients had diffuse intracranial dolichoectasia, and 139 had vertebrobasilar dolichoectasia. Patients with diffuse intracranial dolichoectasia were older than those with vertebrobasilar dolichoectasia (70.9 ± 14.2 years versus 60.4 ± 12.5 years, P = .0002) and had a higher prevalence of abdominal aortic aneurysms (62.5% versus 14.3%, P = .01), other visceral aneurysms (25.0% versus 0%, P < .0001), and smoking (68.0% versus 15.9%, P < .0001). Patients with diffuse intracranial dolichoectasia were more likely to have aneurysm growth (46.2% versus 21.5%, P = .09) and rupture (20% versus 3.5%, P = .007) at follow-up. Patients with diffuse intracranial dolichoectasia were less likely to have good neurologic function at follow-up (24.0% versus 57.6%, P = .004) and were more likely to have aneurysm-related death (24.0% versus 7.2%, P = .02).
Conclusions:
The natural history of patients with diffuse intracranial dolichoectasia is significantly worse than that in those with isolated vertebrobasilar dolichoectasia. Many patients with diffuse intracranial dolichoectasia had additional saccular and abdominal aortic aneurysms. These findings suggest that diffuse intracranial dolichoectasia may be a distinct vascular phenotype secondary to a systemic arteriopathy affecting multiple vascular beds.
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