from Section 2 - Cerebrovascular disease
Published online by Cambridge University Press: 05 March 2013
Basic principles of susceptibility contrast
Magnetic resonance sequences that take advantage of susceptibility effects to demonstrate pathology are powerful and sensitive aids for diagnostic imaging. An important distinction should be highlighted at this point. Although the term susceptibility-weighted imaging (SWI) has been used in the past to refer to T2*-weighted gradient recall echo (GRE) techniques, the more recent convention is to reserve this term for a distinct new sequence utilizing both magnitude and phase information. The bulk of the stroke-related research discussed in this chapter relates to conventional T2*-weighted GRE sequences; susceptibility sequences and SWI are discussed in Ch. 10. In particular, one of the key applications of susceptibility sequences is the identification of hemorrhage and blood products.
The evolution of blood breakdown products undergoes the orderly transition through oxyhemoglobin, deoxyhemoglobin, intracellular methemoglobin, extracellular methemoglobin, and ultimately hemosiderin.[1] The MRI appearance of hemorrhage is determined by the magnetic properties and paramagnetic effects of the hemoglobin breakdown products at different stages of iron oxidation. Deoxyhemoglobin, intracellular methemoglobin, and hemosiderin have many unpaired electrons and these are the paramagnetic breakdown products of hemoglobin.[2–4]
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