Volume 23, Issue 3 pp. 431-436
Case Report

Structural and Metabolic Features of Two Different Variants of Multiple Sclerosis: A PET/MRI Study

Julie Bolcaen MSc

Julie Bolcaen MSc

From the Department of Nuclear Medicine, Ghent University Hospital, Ghent, Belgium (JB, KM, IG); Department of Radiology, Ghent University Hospital, Ghent, Belgium (MA, EA); Department of Neurosurgery, Ghent University Hospital, Ghent, Belgium (GH); and Department of Pathology, Ghent University Hospital, Ghent, Belgium (CVB)

Search for more papers by this author
Marjan Acou MD

Marjan Acou MD

From the Department of Nuclear Medicine, Ghent University Hospital, Ghent, Belgium (JB, KM, IG); Department of Radiology, Ghent University Hospital, Ghent, Belgium (MA, EA); Department of Neurosurgery, Ghent University Hospital, Ghent, Belgium (GH); and Department of Pathology, Ghent University Hospital, Ghent, Belgium (CVB)

Search for more papers by this author
Koen Mertens MSc

Koen Mertens MSc

From the Department of Nuclear Medicine, Ghent University Hospital, Ghent, Belgium (JB, KM, IG); Department of Radiology, Ghent University Hospital, Ghent, Belgium (MA, EA); Department of Neurosurgery, Ghent University Hospital, Ghent, Belgium (GH); and Department of Pathology, Ghent University Hospital, Ghent, Belgium (CVB)

Search for more papers by this author
Giorgio Hallaert MD

Giorgio Hallaert MD

From the Department of Nuclear Medicine, Ghent University Hospital, Ghent, Belgium (JB, KM, IG); Department of Radiology, Ghent University Hospital, Ghent, Belgium (MA, EA); Department of Neurosurgery, Ghent University Hospital, Ghent, Belgium (GH); and Department of Pathology, Ghent University Hospital, Ghent, Belgium (CVB)

Search for more papers by this author
Caroline Van den Broecke MD

Caroline Van den Broecke MD

From the Department of Nuclear Medicine, Ghent University Hospital, Ghent, Belgium (JB, KM, IG); Department of Radiology, Ghent University Hospital, Ghent, Belgium (MA, EA); Department of Neurosurgery, Ghent University Hospital, Ghent, Belgium (GH); and Department of Pathology, Ghent University Hospital, Ghent, Belgium (CVB)

Search for more papers by this author
Eric Achten MD, PhD

Eric Achten MD, PhD

From the Department of Nuclear Medicine, Ghent University Hospital, Ghent, Belgium (JB, KM, IG); Department of Radiology, Ghent University Hospital, Ghent, Belgium (MA, EA); Department of Neurosurgery, Ghent University Hospital, Ghent, Belgium (GH); and Department of Pathology, Ghent University Hospital, Ghent, Belgium (CVB)

Search for more papers by this author
Ingeborg Goethals MD, PhD

Ingeborg Goethals MD, PhD

From the Department of Nuclear Medicine, Ghent University Hospital, Ghent, Belgium (JB, KM, IG); Department of Radiology, Ghent University Hospital, Ghent, Belgium (MA, EA); Department of Neurosurgery, Ghent University Hospital, Ghent, Belgium (GH); and Department of Pathology, Ghent University Hospital, Ghent, Belgium (CVB)

Search for more papers by this author
First published: 28 December 2012
Citations: 29
Ingeborg Goethals, Department of Nuclear Medicine, Ghent University Hospital, De Pintelaan 185, 9000 Ghent, Belgium. E-mail: [email protected].

J Neuroimaging 2013;23:431-436.

Abstract

ABSTRACT

BACKGROUND

Multimodality imaging such as proton magnetic resonance spectroscopy (MRS) and positron emission tomography (PET) have provided information specific to the underlying mechanisms of many brain diseases, including multiple sclerosis (MS).

PURPOSE

To determine the structural and metabolic characterization of two particular variants of MS, namely tumefactive MS and Balo's concentric sclerosis (BCS).

METHODS

Conventional MR imaging, diffusion and perfusion MR, MR spectroscopy and PET imaging with F-18 fluorodeoxyglucose (FDG) and F-18 fluoromethylcholine (FCho) were performed.

RESULTS

In a case with pathologically proven tumefactive MS, magnetic resonance imaging (MRI) showed a pseudotumoral lesion with incomplete ring enhancement, peripheral diffusion restriction, and high choline and lactate peaks on MRS. On follow-up, the lesion showed significant growth. In a case of BCS, MRI showed an onion-like lesion without contrast enhancement or diffusion restriction, and only a moderate increase in choline on MRS. The lesion remained stable on follow-up. On PET, there was no uptake of F-18 FDG in either type of MS lesion. Conversely, uptake of F-18 FCho was moderate in tumefactive MS, whereas no F-18 FCho uptake was noted in the lesion with, on MRI, typical features of BCS.

CONCLUSIONS

Our findings illustrate that metabolic features may differ between variants of MS possibly signifying different disease activity.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.