Ultra-High Contrast MRI: The Whiteout Sign Shown with Divided Subtracted Inversion Recovery (dSIR) Sequences in Post-Insult Leukoencephalopathy Syndromes (PILS).

IF 2.2 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Tomography Pub Date : 2024-06-26 DOI:10.3390/tomography10070074
Paul Condron, Daniel M Cornfeld, Miriam Scadeng, Tracy R Melzer, Gil Newburn, Mark Bydder, Eryn E Kwon, Joshua P McGeown, Geoffrey G Handsfield, Taylor Emsden, Maryam Tayebi, Samantha J Holdsworth, Graeme M Bydder
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Abstract

Ultra-high contrast (UHC) MRI describes forms of MRI in which little or no contrast is seen on conventional MRI images but very high contrast is seen with UHC techniques. One of these techniques uses the divided subtracted inversion recovery (dSIR) sequence, which, in modelling studies, can produce ten times the contrast of conventional inversion recovery (IR) sequences. When used in cases of mild traumatic brain injury (mTBI), the dSIR sequence frequently shows extensive abnormalities in white matter that appears normal when imaged with conventional T2-fluid-attenuated IR (T2-FLAIR) sequences. The changes are bilateral and symmetrical in white matter of the cerebral and cerebellar hemispheres. They partially spare the anterior and posterior central corpus callosum and peripheral white matter of the cerebral hemispheres and are described as the whiteout sign. In addition to mTBI, the whiteout sign has also been seen in methamphetamine use disorder and Grinker's myelinopathy (delayed post-hypoxic leukoencephalopathy) in the absence of abnormalities on T2-FLAIR images, and is a central component of post-insult leukoencephalopathy syndromes. This paper describes the concept of ultra-high contrast MRI, the whiteout sign, the theory underlying the use of dSIR sequences and post-insult leukoencephalopathy syndromes.

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超高对比 MRI:用分割减影反转恢复 (dSIR) 序列显示的感染后白质脑病综合征 (PILS) 的 "白化征"。
超高对比度(UHC)核磁共振成像是指在传统核磁共振成像图像中几乎看不到对比度,但使用超高对比度技术后却能看到非常高的对比度的核磁共振成像形式。其中一种技术使用的是分减反转恢复(dSIR)序列,在模型研究中,其对比度是传统反转恢复(IR)序列的十倍。当用于轻度脑外伤(mTBI)病例时,dSIR 序列经常会显示白质的广泛异常,而在使用传统的 T2-流体衰减红外(T2-FLAIR)序列成像时,这些异常看起来是正常的。在大脑和小脑半球的白质中,这种变化是双侧对称的。这些变化会部分波及胼胝体前后中央和大脑半球的外周白质,被称为 "白化征"。除 mTBI 外,在 T2-FLAIR 图像无异常的甲基苯丙胺使用障碍和格林克氏髓鞘病(延迟性缺氧后白质脑病)中也可见到白化征,它是损伤后白质脑病综合征的核心组成部分。本文介绍了超高对比度磁共振成像的概念、白化征、dSIR 序列使用的基础理论以及损伤后白质脑病综合征。
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来源期刊
Tomography
Tomography Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
2.70
自引率
10.50%
发文量
222
期刊介绍: TomographyTM publishes basic (technical and pre-clinical) and clinical scientific articles which involve the advancement of imaging technologies. Tomography encompasses studies that use single or multiple imaging modalities including for example CT, US, PET, SPECT, MR and hyperpolarization technologies, as well as optical modalities (i.e. bioluminescence, photoacoustic, endomicroscopy, fiber optic imaging and optical computed tomography) in basic sciences, engineering, preclinical and clinical medicine. Tomography also welcomes studies involving exploration and refinement of contrast mechanisms and image-derived metrics within and across modalities toward the development of novel imaging probes for image-based feedback and intervention. The use of imaging in biology and medicine provides unparalleled opportunities to noninvasively interrogate tissues to obtain real-time dynamic and quantitative information required for diagnosis and response to interventions and to follow evolving pathological conditions. As multi-modal studies and the complexities of imaging technologies themselves are ever increasing to provide advanced information to scientists and clinicians. Tomography provides a unique publication venue allowing investigators the opportunity to more precisely communicate integrated findings related to the diverse and heterogeneous features associated with underlying anatomical, physiological, functional, metabolic and molecular genetic activities of normal and diseased tissue. Thus Tomography publishes peer-reviewed articles which involve the broad use of imaging of any tissue and disease type including both preclinical and clinical investigations. In addition, hardware/software along with chemical and molecular probe advances are welcome as they are deemed to significantly contribute towards the long-term goal of improving the overall impact of imaging on scientific and clinical discovery.
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