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Case 18 - Tumefactive demyelinating lesion

Published online by Cambridge University Press:  18 December 2013

Nafi Aygun
Affiliation:
The Johns Hopkins University
Gaurang Shah
Affiliation:
University of Michigan Health System
Dheeraj Gandhi
Affiliation:
University of Maryland Medical Center
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Summary

Imaging description

Demyelinating lesions are usually small and multiple. Occasionally demyelinating lesions can mimic neoplasms clinically, radiologically, and even histologically – hence the name tumefactive demyelinating lesion (TDL). TDLs usually present as large white matter lesions in the periventricular or subcortical regions [1]. In particular, solitary TDLs are often misdiagnosed as tumor, leading to unnecessary biopsy, surgery, and delay in treatment.

While TDLs show a spectrum of imaging abnormalities, certain features are commonly seen, and these help in differentiating TDLs from other lesions [2,3]. On CT, TDLs show hypoattenuation [4]. On post-contrast MRI, incomplete ring enhancement is a relatively characteristic feature, which may be present up to 70% of patients (Figs. 18.1, 18.2). The T2 signal is variable, but most lesions show a markedly increased T2 signal centrally and relatively decreased signal peripherally. Up to 50% of TDLs do not have mass effect or edema, which is a critical observation in differential diagnosis. When mass effect and/or edema present they are usually less pronounced than what would be expected from a high-grade glioma of similar size, although occasionally marked mass effect can be seen. Diffusion-weighted imaging (DWI) signal is also variable across the lesions, with central parts showing increased diffusivity and peripheral potions showing relative restricted diffusion (Fig. 18.1).

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Pearls and Pitfalls in Head and Neck and Neuroimaging
Variants and Other Difficult Diagnoses
, pp. 55 - 57
Publisher: Cambridge University Press
Print publication year: 2013

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References

Cianfoni, A, Niku, S, Imbesi, SG. Metabolite findings in tumefactive demyelinating lesions utilizing short echo time proton magnetic resonance spectroscopy. AJNR Am J Neuroradiol 2007; 28: 272–7.Google ScholarPubMed
Saini, J, Chatterjee, S, Thomas, B, Kesavadas, C. Conventional and advanced magnetic resonance imaging in tumefactive demyelination. Acta Radiol. 2011; 52: 1159–68.CrossRefGoogle ScholarPubMed
Kiriyama, T, Kataoka, H, Taoka, T, et al. Characteristic neuroimaging in patients with tumefactive demyelinating lesions exceeding 30mm. J Neuroimaging 2011; 21: e69–77.CrossRefGoogle Scholar
Kim, DS, Na, DG, Kim, KH, et al. Distinguishing tumefactive demyelinating 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
Blasel, S, Pfeilschifter, W, Jansen, V, et al. Metabolism and regional cerebral blood volume in autoimmune inflammatory demyelinating lesions mimicking malignant gliomas. J Neurol. 2011; 258: 113–22.CrossRefGoogle ScholarPubMed

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