Abstract

White matter signal changes in magnetic resonance imaging (MRI) are frequent and the correct clinical assessment is very important for the further clinical management of the patient. The first problem in the sequence of dealing with these patients is to determine, if a signal change is truly abnormal or a sign of normal aging. The abundance of unspecific signal changes in the brains of normal persons has lead to the creation of the term unknown bright objects (UBO) for these findings. If a white matter lesion is deemed truly abnormal, it should be categorised into one of the major categories such as microvascular, demyelinating, inflammatory, neoplastic or metabolic. Thereafter, a further classification can be attempted. The mainstay of the MRI diagnostics of white matter lesions are dark fluid T 2-weighted sequences such as fluid attenuated inversion recovery (FLAIR). In contrast to conventional T2, these images maintain a high sensitivity for white matter damage in the vicinity of the CSF spaces. T 1-weighted images prior to contrast administration have been shown to demonstrate the clinical significant lesion load whereas the contrast enhanced scan may aid in differential diagnosis and in the evaluation of lesion activity. T 2*-weighted imaging is useful to identify previous microbleeds, which usually occur in microvascular conditions and portend the risk of further bleeding. Proton spectroscopy, chemical shift imaging and diffusion weighted imaging have been shown to be very useful in some entities of white matter disease, both for differential diagnosis and the assessment of disease activity. They should hence be part of any advanced imaging protocol in patients with white matter disease. © Georg Thieme Verlag KG Stuttgart.

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