Evidence map›Paper›PMID 39079712›Full record

ArticleAJNR. American journal of neuroradiology2025

Alternative Venous Pathways: A Potential Key Imaging Feature for Early Diagnosis of Sturge-Weber Syndrome Type 1.

Carmen R Cerron-Vela, Amirreza Manteghinejad, Simon M Clifford, Savvas Andronikou

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Article in AJNR. American journal of neuroradiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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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

4 authors.

Carmen R Cerron-VelaFrom the Children's Hospital of Philadelphia, Philadelphia, Pennsylvania cerronvelc@chop.edu.ORCID 0000-0002-7881-6021
Amirreza ManteghinejadFrom the Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0002-3847-5496
Simon M CliffordFrom the Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0002-2793-4159
Savvas AndronikouFrom the Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0002-1015-9790

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeSturge-Weber syndrome (SWS) is a rare congenital disorder characterized by cortical atrophy and calcifications on late-stage imaging. Understanding the evolution of brain lesions is crucial for effective early interventions, yet the timeline remains unclear. We aimed to evaluate early brain MRI findings and their progression longitudinally on follow-up MRI in children diagnosed with SWS. MATERIALS AND

methodsWe retrospectively included all children with a confirmed diagnosis of SWS between 2009 and 2023 who had at least 2 available MRIs performed before the age of 2 years. A pediatric radiologist and a pediatric neuroradiologist evaluated all the MRI scans for pial enhancement, choroid plexus enlargement, atrophy, calcifications, a prominent subarachnoid varicose network, transmedullary veins, subependymal veins, and deep extraventricular veins. Descriptive analysis was used for demographic data and brain lesion prevalence. Cumulative incidence curves were used to show the timeline of emerging lesions. K-means clustering was used to categorize the lesions based on their prevalence at 1, 2, 3, 6, 12, 18, and 24 months after birth.

resultsNine patients met the inclusion criteria. Median ages at the first and last MRIs were 35 days (interquartile range [IQR]: 11-123) and 294 days (IQR: 208-465), respectively. The most prevalent lesions at the first MRI were subarachnoid varicose network (88.9%) and transmedullary veins (77.8%), while prevalence of atrophy and calcifications differed most between the first and last MRIs. The results of the elbow method and K-means clustering showed that we can divide SWS lesions into 3 groups based on their timeline of emergence. The first cluster contained subarachnoid varicose network, transmedullary veins, subependymal veins, and choroid plexus enlargement. The second cluster contained deep extraventricular veins, pial enhancement, accelerated myelination, and atrophy. The last cluster contained calcifications.

conclusionsOur findings suggest that dilated venous channels emerge early as a compensatory mechanism, preceding atrophy and calcification. Additionally, these dilated channels precede the appearance of abnormal contrast enhancement of the pia, often termed leptomeningeal angioma. This underscores the importance of early recognition and monitoring of these initial imaging indicators in clinical practice.

Indexed as

Early DiagnosisMagnetic Resonance ImagingSturge-Weber SyndromeBrainCerebral VeinsChild, PreschoolFemaleHumansInfantInfant, NewbornMaleRetrospective Studies

Identifiers

PMID39079712
PMCPMC11735450

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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.