Diffuse low-grade oligodendrogliomas extend beyond MRI-defined abnormalities
Citation Manager Formats
Make Comment
See Comments
This article requires a subscription to view the full text. If you have a subscription you may use the login form below to view the article. Access to this article can also be purchased.
Abstract
Background: Imaging determinations of the spatial extent of diffuse low-grade gliomas (DLGGs) are of paramount importance in evaluating the risk-to-benefit ratio of surgical resection. However, it is not clear how accurately preoperative conventional MRI can delineate DLGGs.
Methods: We report a retrospective histologic and imaging correlation study in 16 adult patients who underwent serial stereotactic biopsies for the diagnosis of untreated supratentorial well-defined and non–contrast-enhanced DLGG, in whom biopsy samples were taken within and beyond (OutBSs) MRI-defined abnormalities.
Results: Thirty-seven OutBSs that extended from 10 to 26 mm beyond MRI-defined abnormalities were studied. Immunostaining revealed MIB-1–positive cells (i.e., cycling cells) in all but 2 of the OutBSs. None of the MIB-1–positive cells coexpressed glial fibrillary acidic protein, and all of them coexpressed OLIG2. MIB-1–positive cells were cycling isolated tumor cells, because 1) their morphologic characteristics reflected those of tumor cells, 2) the number of MIB-1–positive cells per square centimeter was significantly higher than that of controls, 3) the number of MIB-1–positive cells per square centimeter was positively correlated with the tumor growth fraction (p = 0.012), and 4) the number of MIB-1–positive cells per square centimeter in OutBSs decreased with distance from the tumor (p = 0.003).
Conclusions: This study demonstrates, using a multiscale correlative approach, that conventional MRI underestimates the actual spatial extent of diffuse low-grade gliomas (DLGGs), even when they are well delineated. These results suggest that an extended resection of a margin beyond MRI-defined abnormalities, whenever feasible in noneloquent brain areas, might improve the outcome of DLGGs.
Glossary
- BS=
- biopsy sample;
- DLGG=
- diffuse low-grade glioma;
- FLAIR=
- fluid-attenuated inversion recovery;
- GFAP=
- glial fibrillary acidic protein;
- H1-MRSI=
- proton magnetic resonance spectroscopic imaging;
- InBS=
- biopsy sample taken inside MRI-defined abnormalities;
- ITC=
- isolated tumor cell;
- MR=
- magnetic resonance;
- NFP=
- neurofilament protein;
- OutBS=
- biopsy sample taken outside MRI-defined abnormalities.
AAN Members
We have changed the login procedure to improve access between AAN.com and the Neurology journals. If you are experiencing issues, please log out of AAN.com and clear history and cookies. (For instructions by browser, please click the instruction pages below). After clearing, choose preferred Journal and select login for AAN Members. You will be redirected to a login page where you can log in with your AAN ID number and password. When you are returned to the Journal, your name should appear at the top right of the page.
AAN Non-Member Subscribers
Purchase access
For assistance, please contact:
AAN Members (800) 879-1960 or (612) 928-6000 (International)
Non-AAN Member subscribers (800) 638-3030 or (301) 223-2300 option 3, select 1 (international)
Sign Up
Information on how to subscribe to Neurology and Neurology: Clinical Practice can be found here
Purchase
Individual access to articles is available through the Add to Cart option on the article page. Access for 1 day (from the computer you are currently using) is US$ 39.00. Pay-per-view content is for the use of the payee only, and content may not be further distributed by print or electronic means. The payee may view, download, and/or print the article for his/her personal, scholarly, research, and educational use. Distributing copies (electronic or otherwise) of the article is not allowed.
Letters: Rapid online correspondence
REQUIREMENTS
You must ensure that your Disclosures have been updated within the previous six months. Please go to our Submission Site to add or update your Disclosure information.
Your co-authors must send a completed Publishing Agreement Form to Neurology Staff (not necessary for the lead/corresponding author as the form below will suffice) before you upload your comment.
If you are responding to a comment that was written about an article you originally authored:
You (and co-authors) do not need to fill out forms or check disclosures as author forms are still valid
and apply to letter.
Submission specifications:
- Submissions must be < 200 words with < 5 references. Reference 1 must be the article on which you are commenting.
- Submissions should not have more than 5 authors. (Exception: original author replies can include all original authors of the article)
- Submit only on articles published within 6 months of issue date.
- Do not be redundant. Read any comments already posted on the article prior to submission.
- Submitted comments are subject to editing and editor review prior to posting.
You May Also be Interested in
Long-term Safety and Efficacy of Avalglucosidase Alfa in Patients With Late-Onset Pompe Disease
Dr. Marianne de Visser and Dr. Maudy Theunissen
► Watch
Topics Discussed
Alert Me
Recommended articles
-
Articles
Diagnostic performance of spectroscopic and perfusion MRI for distinction of brain tumorsM. A. Weber, S. Zoubaa, M. Schlieter et al.Neurology, June 26, 2006 -
Article
Developmental venous anomaly in adult patients with diffuse gliomaA clinically relevant coexistence?Alexandre Roux, Myriam Edjlali, Sayuri Porelli et al.Neurology, November 30, 2018 -
Articles
Temporal lobe abnormalities on brain MRI in healthy volunteersA prospective case-control studyA. Labate, A. Gambardella, U. Aguglia et al.Neurology, January 20, 2010 -
Article
Three-tesla functional MR language mappingComparison with direct cortical stimulation in gliomasGrégory Kuchcinski, Charles Mellerio, Johan Pallud et al.Neurology, January 14, 2015