Evidence map›Paper›PMID 40782678›Full record

ArticlePediatric neurology2025

Absence of Deep and Basal Veins Is Common and Clinically Relevant in Sturge-Weber Syndrome.

Fatimah M Albazron, E Mark Haacke, Ajay Kumar, Sagar Buch, Yang Xuan, Jeong-Won Jeong, Aimee F Luat, Michael E Behen, Nore Gjolaj, Csaba Juhász

Abstract read
In one paragraph

Article in Pediatric neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Fatimah M AlbazronDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit Michigan; Translational Imaging Laboratory, Wayne State University School of Medicine, Detroit, Michigan.
E Mark HaackeDepartment of Radiology, Wayne State University School of Medicine, Detroit, Michigan; Department of Neurology, Wayne State University School of Medicine, Detroit, Michigan; Department of Biomedical Engineering, Wayne State University, Detroit, Michigan; Wayne State University MR Core Research Facility, Detroit, Michigan.
Ajay KumarDivision of Neuroradiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Pediatrics, Wayne State University School of Medicine, Detroit, Michigan.
Sagar BuchDepartment of Neurology, Wayne State University School of Medicine, Detroit, Michigan.
Yang XuanWayne State University MR Core Research Facility, Detroit, Michigan.
Jeong-Won JeongTranslational Imaging Laboratory, Wayne State University School of Medicine, Detroit, Michigan; Department of Neurology, Wayne State University School of Medicine, Detroit, Michigan; Department of Pediatrics, Wayne State University School of Medicine, Detroit, Michigan.
Aimee F LuatDepartment of Pediatrics, Wayne State University School of Medicine, Detroit, Michigan; Department of Pediatrics, Central Michigan University, Mt Pleasant, Michigan; Children's Hospital of Michigan, Detroit, Michigan.
Michael E BehenTranslational Imaging Laboratory, Wayne State University School of Medicine, Detroit, Michigan; Department of Neurology, Wayne State University School of Medicine, Detroit, Michigan; Department of Pediatrics, Wayne State University School of Medicine, Detroit, Michigan.
Nore GjolajDepartment of Pediatrics, Wayne State University School of Medicine, Detroit, Michigan.
Csaba JuhászTranslational Imaging Laboratory, Wayne State University School of Medicine, Detroit, Michigan; Department of Neurology, Wayne State University School of Medicine, Detroit, Michigan; Department of Pediatrics, Wayne State University School of Medicine, Detroit, Michigan. Electronic address: csaba.juhasz@wayne.edu.

Funding

Longitudinal Neuroimaging in Sturge-Weber SyndromeR01NS041922 · NINDS · WAYNE STATE UNIVERSITY · PI JUHASZ, CSABA · 2003 to 2024
$6.2M
NINDS NIH HHS R01 NS041922
6 · The paper itself

Abstract

backgroundCommon intracranial vascular abnormalities in Sturge-Weber syndrome (SWS) include leptomeningeal venous malformations (LVMs) and enlarged deep veins. A few small studies have reported absent deep veins in some patients. We used susceptibility-weighted imaging (SWI), a magnetic resonance imaging (MRI) sequence sensitive to detecting small veins, to evaluate deep cerebral veins and the basal vein of Rosenthal (BVR) and assess the radiological correlates and clinical impact of their absence.

methodsFifty young subjects, including 30 patients with unilateral SWS and 20 healthy controls, underwent 3T brain MRI prospectively. The presence or absence of the internal cerebral vein (ICV), its two main tributaries, and the BVR were evaluated on SWI in all 50 subjects and correlated with other brain abnormalities and clinical symptoms in the SWS group.

resultsAlthough deep veins and the BVR were identified bilaterally in all control subjects, absent veins were observed in 70% of patients with SWS: in the SWS-affected hemisphere, absent ICV in 15 (50%), thalamostriate vein in 11 (37%), septal vein in seven (23%), and BVR in nine (30%) patients. Absent contralateral veins were also observed. Absent veins were associated with enlarged and collateral veins. Absent BVR and ICV were associated with extensive LVM, brain atrophy, and worse motor functions (P < 0.05); absent BVR was also associated with stroke-like episodes.

conclusionsAbsence of deep and/or basal cerebral veins is common in SWS and is associated with venous vascular anomalies, parenchymal damage, and motor impairment. Absent BVR may also increase the risk for stroke-like episodes.

Indexed as

BrainCerebral VeinsSturge-Weber SyndromeAdolescentAdultChildChild, PreschoolFemaleHumansMagnetic Resonance ImagingMaleProspective StudiesYoung AdultBasal veinsDeep cerebral veinsMagnetic resonance imagingMotor functionsStroke-like episodesSturge-Weber syndromeSusceptibility-weighted imaging

Identifiers

PMID40782678
PMCPMC12762158

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.