Object Early postoperative MRI within 72 hours after brain tumor surgery is commonly used to assess residual contrast-enhancing tumor. The 72-hour window is commonly accepted because previous 1.5-T MRI studies have not found confounding postoperative reactive contrast enhancement in this time frame. The sensitivity to detect contrast enhancement increases with the field strengths. Therefore, the authors aimed to assess whether the 72-hour window is also appropriate for the MRI scanner with a field strength of 3 T. Methods The authors retrospectively analyzed findings on early postsurgical MR images acquired in 46 patients treated for high-grade gliomas. They performed 3-T MRI within 7 days before surgery and within 72 hours thereafter. The appearance of enhancement was categorized as postoperative reactive enhancement or tumoral enhancement by comparison with the pattern and location of presurgical enhancing tumor. Results Postoperative reactive enhancement was present in 15 patients (32.6%). This enhancement, not seen on presurgical MRI, had a marginal or leptomeningeal/dural pattern. In 13 patients (28.3%) postsurgical enhancement was found within the first 72 postoperative hours, with the earliest seen 22:57 hours after surgery. Subsequent MR scans in patients with postoperative reactive enhancement did not reveal tumor recurrence in these regions. Conclusions Postoperative reactive enhancement earlier than 72 hours after brain tumor surgery can be expected in about one-third of the cases in which a 3-T scanner is used. This might be due to the higher enhancement-to-brain contrast at higher field strengths. Therefore, the time window of 72 hours does not prevent reactive enhancement, which, however, can be recognized as such comparing it with presurgical enhancing tumor.

Intraoperative MRI (iMRI) allows a more detailed appreciation of the extent of resection than does conventional neurosurgery and results in longer overall survival in patients with malignant glioma. However, it is unknown whether the intraoperative application of contrast agent influences the early postsurgical MRI. The preceding iMRI could alter the signals of MR sequences in the early postsurgical MRI, especially in sequences influenced by T1 contrast. Hereby, we investigate such iMRI-induced influences on the fluid-attenuated inversion recovery (FLAIR) sequence. We retrospectively analyzed postsurgical T2w, T1w, and FLAIR images by visual inspection and by signal measurements in 46 patients with malignant gliomas after tumor resection. Of these, n = 25 patients were operated with conventional microsurgery, and n = 21 patients were operated with contrast-enhanced iMRI-guided microsurgery. We measured signal intensity in the resection cavity, in the cerebrospinal fluid (CSF) of the ventricles, and in the normal brain tissue contralateral to the tumor-bearing hemisphere on axial FLAIR images and T1-weighted and T2-weighted images. In 18 patients, the FLAIR sequence revealed hyperintense signal changes of the CSF in the subarachnoid or ventricular spaces. Seventeen of these 18 patients had received intraoperative MRI. In both FLAIR and T1-weighted images, the signal of the CSF in the ventricles was significantly higher in patients with iMRI than in patients without iMRI. The intraoperative application of contrast agent that is used for iMRI significantly influences postsurgical MRI within the first 72 h. We found hyperintense signal changes of the CSF in the FLAIR sequence in the subarachnoid and intraventricular spaces mimicking subarachnoid hemorrhage. The findings may result in a misdiagnosis of subarachnoid hemorrhage (SAH) in these patients.