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DOI: 10.1055/s-0045-1813663
Incremental Role of Spinal Diffusion-Weighted Imaging in the Detection of Leptomeningeal Metastasis for Pediatric Intracranial Malignancies: Results from a Prospective Study
Authors
Funding None.
Abstract
Background
Screening for leptomeningeal disease (LMD) in pediatric brain tumors on the magnetic resonance imaging protocol is often limited by artifacts, making diagnosis challenging.
Objectives
To prospectively evaluate the incremental role of diffusion-weighted imaging (DWI) in screening of LMD in pediatric brain tumors.
Materials and Methods
This prospective study included pediatric patients with primary brain tumors having a propensity for cerebrospinal fluid (CSF) metastasis. The spine was screened with T2-weighted (T2W), DWI, and post-contrast T1W (T1W PC) sequences, and LMD was confirmed with CSF analysis and follow-up.
Results
The study included 69 patients. LMD was positive in 27 patients and 105 lesions. Smooth LMD was detected in 18 patients on T1W PC. Out of 85 nodular LMD lesions, 81 were detected on DWI. Six lesions on the T1W PC and 16 on T2W were false positives (artifacts). The sensitivity and specificity were: for T1W PC: 93 and 86%; T2W: 63 and 62%; and for DWI: 63 and 100%. The combined sensitivity, specificity, positive predictive value, and negative predictive value of all three sequences were 93, 100, 100, and 95%.
Conclusion
The T1W PC sequence is the most reliable sequence for detecting LMD. Using DWI in conjunction with T1W PC and T2W excludes artifacts, resulting in a higher specificity.
Patient Consent
Waiver of consent was obtained from the institutional ethics committee as this was a retrospective study with less than minimal risk.
Publication History
Article published online:
01 December 2025
© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
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