Evidence map›Paper›PMID 39570401›Full record

ArticleNeuroradiology2025

T2/FLAIR mismatch and diffusion restriction as novel pathophysiological markers in MRI evaluation of central tegmental tract hyperintensity in pediatric patients.

Emre Utkan Buyukceran, Seda Kaynak Sahap, Sinan Genc, Suat Fitoz

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

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Emre Utkan BuyukceranDepartment of Radiology, Igdir State Hospital, Igdir, Turkey. utkan.buyukceran91@gmail.com.ORCID http://orcid.org/0000-0001-6912-7737
Seda Kaynak SahapDepartment of Pediatric Radiology, Faculty of Medicine, Ankara University, Ankara, Turkey.ORCID http://orcid.org/0000-0003-1283-9543
Sinan GencDepartment of Pediatric Radiology, Dr. Behçet Uz Health Research Center For Paediatric Diseases And Surgery, İzmir, Turkey.ORCID http://orcid.org/0000-0003-2634-7515
Suat FitozDepartment of Pediatric Radiology, Faculty of Medicine, Ankara University, Ankara, Turkey.ORCID http://orcid.org/0000-0002-0180-0013

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCentral tegmental tract hyperintensity (CTTH) on T2-weighted imaging is an uncommon neuroimaging finding in pediatric patients with unclear clinical significance. CTTH may represent either a physiological or pathological process. This study evaluates the relationship between CTTH and MRI sequences (FLAIR, DWI) to explore its diagnostic value.

methodsWe retrospectively analyzed 3462 pediatric brain MRI scans conducted between July 2011 and January 2022, identifying 104 patients with bilateral CTTH. DWI, FLAIR sequences, and follow-up scans were visually assessed for T2/FLAIR mismatch and diffusion restriction. Clinical data were obtained from electronic patient records. Statistical analysis was performed using SPSS, with significance set at p < .05.

resultsA total of 104 pediatric patients with CTTH were included, ranging from 1 month to 16 years old (mean age: 31.34 months). Epilepsy, metabolic diseases, and cerebral palsy were the most common clinical diagnoses. Diffusion restriction was observed in 40.8% of patients, while 39.6% had FLAIR hyperintensity. T2/FLAIR mismatch, defined for the first time in CTTH, was found in 60.4% of patients. A significant correlation was found between T2/FLAIR mismatch and clinical diagnoses (p = .020), as well as between diffusion restriction and T2/FLAIR mismatch (p = .017).

conclusionCTTH in pediatric patients may arise from two distinct processes: a transient, developmental phenomenon or a pathological process marked by irreversible myelin degeneration. T2/FLAIR mismatch and diffusion restriction provide valuable diagnostic markers, offering insights into the severity and chronicity of CTTH. Further studies are needed to validate these findings and their clinical implications.

Indexed as

Brain DiseasesDiffusion Magnetic Resonance ImagingMagnetic Resonance ImagingNeuroimagingAdolescentChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesCentral tegmental tract hyperintensityCTTHDiffusion-weighted imagingDWIFLAIR sequencesPathophysiological markersPediatric neuroimagingT2/FLAIR mismatchT2-weighted imaging

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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.