# Neurovascular Issues in Neurofibromatosis Type I: Focus on Intracranial Stenosis

**Authors:** Marialuisa Zedde, Rosario Pascarella

PMC · DOI: 10.3390/life16020234 · 2026-02-01

## TL;DR

This paper reviews neurovascular complications in Neurofibromatosis Type I, focusing on intracranial stenosis and highlighting the need for better diagnosis and treatment.

## Contribution

The paper synthesizes current knowledge on intracranial stenosis in NF1, emphasizing differences between pediatric and adult populations.

## Key findings

- Intracranial vasculopathy affects 0.4% to 6.4% of NF1 patients, with higher stenotic lesion rates in children.
- Vascular abnormalities in adults are less understood, with 3.5% of adult NF1 patients affected.
- Routine use of MRA is lacking, leading to underdiagnosis of vascular issues in NF1 patients.

## Abstract

Background/Objectives: Neurofibromatosis type 1 (NF1) is a genetic disorder characterized by various clinical manifestations, including significant neurovascular complications. This review aims to synthesize current knowledge regarding intracranial stenoses and associated vascular abnormalities in patients with NF1, emphasizing the differences between pediatric and adult populations. Methods: A narrative review was conducted, analyzing the existing literature on the epidemiology, clinical manifestations, and management of neurovascular issues related to NF1. Data were collected from a range of studies, including retrospective analyses and case series, focusing on the incidence and outcomes of intracranial vascular abnormalities. Results: The study found that intracranial vasculopathy affects between 0.4% and 6.4% of NF1 patients, with children experiencing higher rates of stenotic lesions. However, vascular issues in adults are less understood, with 3.5% of adult patients presenting vascular abnormalities. The review highlights a significant underdiagnosis of these conditions due to the lack of routine use of magnetic resonance angiography (MRA) in standard evaluations. The management of NF1-related vascular conditions, particularly in adults, remains poorly defined, particularly regarding the efficacy of antithrombotic therapies. Conclusions: The management of neurovascular complications in NF1 requires urgent attention, with a need for standardized screening protocols and further research to elucidate the natural history and optimal treatment strategies for these patients. Enhanced diagnostic practices, including routine neuroimaging, are essential to improve outcomes and reduce the risk of significant vascular events.

## Linked entities

- **Diseases:** Neurofibromatosis type 1 (MONDO:0018975)

## Full-text entities

- **Genes:** NF1 [NCBI Gene 531372], Ccl2 (C-C motif chemokine ligand 2) [NCBI Gene 20296] {aka HC11, JE, MCAF, MCP-1, MCP1, SMC-CF}, RNF213 (ring finger protein 213) [NCBI Gene 57674] {aka ALO17, C17orf27, KIAA1618, MYMY2, MYSTR, NET57}, ACTA2 (actin alpha 2, smooth muscle) [NCBI Gene 59] {aka ACTSA, SMDYS}, Nf1 (neurofibromin 1) [NCBI Gene 18015] {aka Dsk9, E030030H24Rik, Mhdadsk9, Nf-1}, Ccr2 (C-C motif chemokine receptor 2) [NCBI Gene 12772] {aka Cc-ckr-2, Ccr2a, Ccr2b, Ckr2, Ckr2a, Ckr2b}, Mapk1 (mitogen-activated protein kinase 1) [NCBI Gene 26413] {aka 9030612K14Rik, ERK, Erk2, MAPK2, PRKM2, Prkm1}, NF1 (neurofibromin 1) [NCBI Gene 4763] {aka NFNS, VRNF, WSS}, NF1 (neurofibromin 1) [NCBI Gene 280877]
- **Diseases:** Lisch nodules (MESH:C567588), neurocutaneous disorder (MESH:D020752), head and neck cancers (MESH:D006258), hemorrhagic stroke (MESH:D000083302), Aneurysms (MESH:D000783), Vasculopathy (MESH:D000090122), aplasia (MESH:C536482), tumor (MESH:D009369), vessel abnormalities (MESH:C536223), chromosomal abnormalities (MESH:D002869), Vascular Abnormalities (MESH:D014652), cerebral ischemia (MESH:D002545), dissection (MESH:D000784), ruptures (MESH:D012421), paramedian diencephalic syndrome (MESH:D007027), visual deficiencies (MESH:D014786), optic nerve glioma (MESH:D020339), vessel ectasia (MESH:D004108), inflammation (MESH:D007249), conditions (MESH:D020763), headaches (MESH:D006261), injury to (MESH:D014947), brachial artery aneurysm (MESH:D002532), fibromuscular hyperplasia (MESH:D005352), ectasia of the cerebral arteries (MESH:D002539), gliomas (MESH:D005910), congenital anomalies (MESH:D000013), Siderosis (MESH:D012806), orbitofacial masses (MESH:C536030), aneurysmal formations (MESH:D058426), arteriopathy (MESH:D020212), arm swelling (MESH:D001134), sensorineural hearing loss (MESH:D006319), autosomal dominant disorder (MESH:D030342), PHACE syndrome (MESH:C537892), Intracranial stenosis (MESH:D003251), Neurofibromatosis Type I (MESH:D009456), cerebellar stroke (MESH:D002526), vascular complications (MESH:D003925), vascular malformation (MESH:D054079), Stroke (MESH:D020521), acquired abnormalities (MESH:D000163), hemorrhage (MESH:D006470), aortic stenosis (MESH:D001024), venous thrombosis (MESH:D020246), bone lesions (MESH:D001847), macrophage dysfunction (MESH:D055501), pulmonary artery stenosis (MESH:D000071079), cerebrovascular abnormalities (MESH:D002561), cardiovascular disorders (MESH:D002318), arterial stenosis (MESH:D012078), ischemic strokes (MESH:D002544), ischemic damage (MESH:D017202), neurovascular abnormalities (MESH:D013901), cerebral vasculopathy (MESH:C566007), arterial stenosis/occlusion (MESH:D001157), hypertension (MESH:D006973), sphenoid wing dysplasia (MESH:D008579), arterial hypertension (MESH:D000081029), aneurysmal subarachnoid hemorrhage (MESH:D013345)
- **Chemicals:** antiplatelet (-), lipid (MESH:D008055)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913]
- **Mutations:** p.(Arg1276*), p.Arg1809Cys, A1 ACA, c.3826C>T

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941482/full.md

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Source: https://tomesphere.com/paper/PMC12941482