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159 - Tumefactive Demyelinating Lesion

from Section 6 - Primarily Intra-Axial Masses

Published online by Cambridge University Press:  05 August 2013

Zoran Rumboldt
Affiliation:
Medical University of South Carolina
Zoran Rumboldt
Affiliation:
Medical University of South Carolina
Mauricio Castillo
Affiliation:
University of North Carolina, Chapel Hill
Benjamin Huang
Affiliation:
University of North Carolina, Chapel Hill
Andrea Rossi
Affiliation:
G. Gaslini Children's Research Hospital
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Summary

Specific Imaging Findings

Mass-like features of multiple sclerosis and other demyelinating processes are referred to as tumefactive demyelinating lesions (TDLs). TDLs are typically located in the cerebral white matter ranging from 1 to over 10 cm in size. They may be unifocal; however, additional lesions are usually either present or occur over time. Edema surrounds most TDLs, but is usually very mild, and mass effect is typically even less prominent. The lesions are T1 hypointense in the center and their periphery may be brighter on magnetization transfer imaging. Almost all TDLs enhance with contrast, which may co-localize with a T2 hypointense rim. Incomplete rim enhancement (“open ring”), along with mixed T2 iso- and hyperintensity of the enhancing components, absence of cortical involvement, and absence of mass effect are highly specific for TDL, but not always present. Vessel-like structures, presumably veins, running through the lesion are typical but only occasionally seen. Other characteristic features are bright peripheral rim on DWI (dark on ADC maps) and relatively low rCBV on perfusion studies. CT hypodensity of the enhanced regions on MRI (the MRI enhancing rim is not discernible on non-enhanced CT) is also very specific. Marked elevation of glutamate and glutamine (Glx, at 2.1–2.5 ppm) are characteristically present on short echo time (TE around 30 ms) MR spectroscopy. Nonspecific findings are commonly observed with intermediate echo times.

Type
Chapter
Information
Brain Imaging with MRI and CT
An Image Pattern Approach
, pp. 329 - 330
Publisher: Cambridge University Press
Print publication year: 2012

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References

1. Kim, DS, Na, DG, Kim, HK, et al.Distinguishing tumefactive demyelination lesions from glioma or central nervous system lymphoma: added value of unenhanced CT compared with conventional contrast-enhanced MR imaging. Radiology 2009;251:467–75.CrossRefGoogle ScholarPubMed
2. Lucchinetti, CF, Gavrilova, RH, Metz, I, et al.Clinical and radiographic spectrum of pathologically confirmed tumefactive multiple sclerosis. Brain 2008;131:1759–75.CrossRefGoogle ScholarPubMed
3. Jain, R, Ellika, S, Lehman, NL, et al.Can permeability measurements add to blood volume measurements in differentiating tumefactive demyelinating lesions from high grade gliomas using perfusion CT?J Neurooncol 2010;97:383–8.CrossRefGoogle ScholarPubMed
4. Cianfoni, A, Niku, S, Imbesi, SG. Metabolite findings in tumefactive demyelinating lesions utilizing short echo time proton magnetic resonance spectroscopy. AJNR 2007;28:272–7.Google ScholarPubMed
5. Given, CA 2nd, Stevens, BS, Lee, C. The MRI appearance of tumefactive demyelinating lesions. AJR 2004;182:195–9.CrossRefGoogle ScholarPubMed

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