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

IF 2.4 3区 医学 Q2 CLINICAL NEUROLOGY Neuroradiology Pub Date : 2024-11-21 DOI:10.1007/s00234-024-03509-6
Emre Utkan Buyukceran, Seda Kaynak Sahap, Sinan Genc, Suat Fitoz
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Abstract

Introduction: Central 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.

Methods: We 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.

Results: A 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).

Conclusion: CTTH 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.

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T2/FLAIR错配和弥散限制作为新的病理生理标记,用于对儿科患者的中央被盖束高密度进行磁共振成像评估。
简介T2加权成像上的中央被盖束高密度(CTTH)是儿科患者中一种不常见的神经影像学发现,其临床意义尚不明确。CTTH 可能代表生理或病理过程。本研究评估了 CTTH 与 MRI 序列(FLAIR、DWI)之间的关系,以探讨其诊断价值:我们回顾性分析了 2011 年 7 月至 2022 年 1 月期间进行的 3462 例小儿脑部 MRI 扫描,发现 104 例双侧 CTTH 患者。我们对 DWI、FLAIR 序列和随访扫描进行了视觉评估,以确定是否存在 T2/FLAIR 不匹配和弥散受限。临床数据来自电子病历。使用 SPSS 进行统计分析,显著性以 p 为标准:共纳入 104 名 CTTH 儿童患者,年龄从 1 个月到 16 岁不等(平均年龄:31.34 个月)。癫痫、代谢性疾病和脑瘫是最常见的临床诊断。40.8%的患者出现弥散受限,39.6%出现FLAIR高密度。60.4%的患者发现了T2/FLAIR不匹配,这在CTTH中尚属首次。T2/FLAIR不匹配与临床诊断(p = .020)以及弥散受限与T2/FLAIR不匹配(p = .017)之间存在明显相关性:结论:儿童患者的 CTTH 可能源于两种不同的过程:一种是短暂的发育现象,另一种是以不可逆转的髓鞘变性为特征的病理过程。T2/FLAIR错配和弥散受限提供了有价值的诊断标记,有助于了解CTTH的严重程度和慢性程度。还需要进一步的研究来验证这些发现及其临床意义。
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来源期刊
Neuroradiology
Neuroradiology 医学-核医学
CiteScore
5.30
自引率
3.60%
发文量
214
审稿时长
4-8 weeks
期刊介绍: Neuroradiology aims to provide state-of-the-art medical and scientific information in the fields of Neuroradiology, Neurosciences, Neurology, Psychiatry, Neurosurgery, and related medical specialities. Neuroradiology as the official Journal of the European Society of Neuroradiology receives submissions from all parts of the world and publishes peer-reviewed original research, comprehensive reviews, educational papers, opinion papers, and short reports on exceptional clinical observations and new technical developments in the field of Neuroimaging and Neurointervention. The journal has subsections for Diagnostic and Interventional Neuroradiology, Advanced Neuroimaging, Paediatric Neuroradiology, Head-Neck-ENT Radiology, Spine Neuroradiology, and for submissions from Japan. Neuroradiology aims to provide new knowledge about and insights into the function and pathology of the human nervous system that may help to better diagnose and treat nervous system diseases. Neuroradiology is a member of the Committee on Publication Ethics (COPE) and follows the COPE core practices. Neuroradiology prefers articles that are free of bias, self-critical regarding limitations, transparent and clear in describing study participants, methods, and statistics, and short in presenting results. Before peer-review all submissions are automatically checked by iThenticate to assess for potential overlap in prior publication.
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