Predicting intraoperative meningioma consistency using features from standard MRI sequences: a preoperative evaluation
- PMID: 40542946
- PMCID: PMC12182493
- DOI: 10.1007/s00701-025-06582-9
Predicting intraoperative meningioma consistency using features from standard MRI sequences: a preoperative evaluation
Abstract
Background: Symptomatic meningiomas may require surgical resection to save or improve neurological function. The extent of tumor resection depends on multiple factors, including the tumor's consistency, its location, and the patient's overall condition. This prospective study aims to explore new criteria in combination with previously proposed tumor features on MRI to establish a rapid approach to tumor consistency characterization pre-operatively.
Methods: Forty-eight patients with meningiomas were prospectively included and underwent a dedicated MRI protocol prior to surgery. Qualitative and quantitative MRI characteristics of the tumor were correlated to a previously proposed surgical tumor consistency grading.
Results: Soft tumors were associated with homogeneous contrast enhancement, high T2 signal, absence of peritumoral edema (PTE), the presence of tumor cysts, and a uniformly dark appearance on fractional anisotropy (FA) maps. In contrast, firmer tumors were characterized by heterogeneous contrast enhancement, low T2 signal, the presence of PTE, absence of tumor cysts and a heterogeneous appearance on FA maps, requiring supranormal ultrasonic aspirator settings. Tumor signal quantification on T2 and Apparent Diffusion Coefficient maps (ADC) correlated moderately to tumor consistency. T1 sequences did not contribute in determining tumor consistency.
Conclusion: An array of simple qualitative meningioma characteristics on MRI can assist in swift discrimination of soft and hard tumors preoperatively. These have been displayed in a figure that can easily be implemented clinically for optimal surgical planning.
Keywords: Consistency; MRI; Meningioma; Tumor.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval: All procedures involving human participants in this study were conducted according to the ethical standards of the 1964 Declaration of Helsinki and its later amendments, or comparable ethical standards. The study was approved by the Regional Research Ethics Committee (REC reference number 20446 (2017/1875)) of Helse Sør-Øst and the Institutional Review Board (IRB) of Oslo University Hospital (PVO reference number 20/00819). Consent to participate: All patient’s informed written consent to participate in this study was collected. Consent for publication: Informed consent was obtained from all individual participants in the study. Competing interest: The authors declare no competing interests. The authors declare no competing interests.
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