J Korean Neurosurg Soc.  2016 Jul;59(4):405-409. 10.3340/jkns.2016.59.4.405.

Experience with 7.0 T MRI in Patients with Supratentorial Meningiomas

Affiliations
  • 1Department of Neurosurgery, Seoul National University College of Medicine, Seoul, Korea. paeksh@snu.ac.kr
  • 2Department of Neurosurgery, Konkuk University Medical Center, Seoul, Korea.
  • 3Neuroscience Research Institute, Gachon University of Medicine and Science, Incheon, Korea.
  • 4Department of Neurosurgery, Seoul National University Hospital, Seoul, Korea.

Abstract

Meningiomas are typically diagnosed by their characteristic appearance on conventional magnetic resonance imaging (MRI). However, detailed image findings regarding peri- and intra-tumoral anatomical structures, tumor consistency and vascularity are very important in pre-surgical planning and surgical outcomes. At the 7.0 T MRI achieving ultra-high resolution, it could be possible to obtain more useful information in surgical strategy. Four patients who were radiologically diagnosed with intracranial meningioma in 1.5 T MRI underwent a 7.0 T MRI. Three of them underwent surgery afterwards, and one received gamma knife radiosurgery. In our study, the advantages of 7.0 T MRI over 1.5 T MRI were a more detailed depiction of the peri- and intra-tumoral vasculature and a clear delineation of tumor-brain interface. In the safety issues, all patients received 7.0 T MRI without any adverse event. One disadvantage of 7.0 T MRI was the reduced image quality of skull base lesions. 7.0 T MRI in patients with meningiomas could provide useful information in surgical strategy, such as the peri-tumoral vasculature and the tumor-brain interface.

Keyword

7.0 T MRI; Meningioma

MeSH Terms

Humans
Magnetic Resonance Imaging*
Meningioma*
Radiosurgery
Skull Base

Figure

  • Fig. 1 A : A trans-axial T2-weighted image on 1.5 T MRI shows a left parieto-occipital, extra-axial mass. B : A left external carotid angiogram shows the arterial supply of the tumor from the middle meningeal artery. C : The intra-tumoral vasculature (closed arrow) and peri-tumoral vasculature (open arrow) are well delineated in 7.0 T MRI.

  • Fig. 2 A : T2-weighted axial image in case 1 shows focal peritumoral edema. In this area, a cerebrospinal fluid cleft is present, and the tumor-brain interface seems to be intact on 1.5 T MRI (closed arrow). B : Intraoperatively, some areas in which the tumor-brain interface was less obvious (open arrow). C : Serial T2-weighted images in 7.0 T MRI provide a more detailed description about the tumor-brain interface. On 7.0 T MRI, the cerebrospinal fluid cleft is not present around the peri-tumoral edema (arrow), and this result is consistent with intraoperative findings.

  • Fig. 3 A : The 1.5 T MRI shows an extra-axial mass in the right frontal lobe. B : The right external carotid angiogram shows that enlarged middle meningeal arteries supply the center of a convex meningioma. C : A T2-weighted axial image on 7.0 T MRI shows more detailed intra-tumoral vasculature than 1.5 T MRI. D : The vessel appearance in T2-weighted sagittal 7.0 T MRI closely resembles angiography.

  • Fig. 4 A : An axial contrast-enhanced T1-weighted image on 1.5 T MRI shows a cortical draining vein (open arrows). B : A T2-weighted image on 7.0 T MRI provides detailed peri-tumoral vasculature, including cortical draining veins (closed arrows) and a vein attached to the tumor capsule (arrowhead).

  • Fig. 5 A : Coronal contrast-enhanced T1-weighted image on 1.5 T MRI shows a well-enhanced mass, which invades the cavernous sinus and encases the internal carotid artery. B : An image of the anatomy below the level of the sylvian fissure is compromised by artifacts in 7.0 T MRI.


Reference

1. Abduljalil AM, Robitaille PM. Macroscopic susceptibility in ultra high field MRI. J Comput Assist Tomogr. 1999; 23:832–841. PMID: 10589555.
Article
2. Abduljalil AM, Schmalbrock P, Novak V, Chakeres DW. Enhanced gray and white matter contrast of phase susceptibility-weighted images in ultra-high-field magnetic resonance imaging. J Magn Reson Imaging. 2003; 18:284–290. PMID: 12938122.
Article
3. Bitzer M, Wöckel L, Luft AR, Wakhloo AK, Petersen D, Opitz H, et al. The importance of pial blood supply to the development of peritumoral brain edema in meningiomas. J Neurosurg. 1997; 87:368–373. PMID: 9285600.
Article
4. Cha S, Johnson G, Wadghiri YZ, Jin O, Babb J, Zagzag D, et al. Dynamic, contrast-enhanced perfusion MRI in mouse gliomas : correlation with histopathology. Magn Reson Med. 2003; 49:848–855. PMID: 12704767.
Article
5. Giombini S, Solero CL, Lasio G, Morello G. Immediate and late outcome of operations for Parasagittal and falx meningiomas. Report of 342 cases. Surg Neurol. 1984; 21:427–435. PMID: 6710323.
Article
6. Ide M, Jimbo M, Kubo O, Yamamoto M, Imanaga H. Peritumoral brain edema associated with meningioma--histological study of the tumor margin and surrounding brain. Neurol Med Chir (Tokyo). 1992; 32:65–71. PMID: 1376862.
7. Kollia K, Maderwald S, Putzki N, Schlamann M, Theysohn JM, Kraff O, et al. First clinical study on ultra-high-field MR imaging in patients with multiple sclerosis : comparison of 1.5T and 7T. AJNR Am J Neuroradiol. 2009; 30:699–702. PMID: 19147714.
Article
8. Lupo JM, Banerjee S, Hammond KE, Kelley DA, Xu D, Chang SM, et al. GRAPPA-based susceptibility-weighted imaging of normal volunteers and patients with brain tumor at 7 T. Magn Reson Imaging. 2009; 27:480–488. PMID: 18823730.
Article
9. Moenninghoff C, Maderwald S, Theysohn JM, Kraff O, Ladd ME, El Hindy N, et al. Imaging of adult astrocytic brain tumours with 7 T MRI : preliminary results. Eur Radiol. 2010; 20:704–713. PMID: 19763581.
Article
10. Norris DG. High field human imaging. J Magn Reson Imaging. 2003; 18:519–529. PMID: 14579394.
Article
11. Thomas DL, De Vita E, Roberts S, Turner R, Yousry TA, Ordidge RJ. High-resolution fast spin echo imaging of the human brain at 4.7 T : implementation and sequence characteristics. Magn Reson Med. 2004; 51:1254–1264. PMID: 15170847.
Article
Full Text Links
  • JKNS
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr