2022
DOI: 10.1148/radiol.213310
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Abbreviated Screening MRI for Women with a History of Breast Cancer: Comparison with Full-Protocol Breast MRI

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Cited by 25 publications
(13 citation statements)
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“…For example, Cheng et al discovered that ZnGa 2 O 4 :Cr 3+ (ZGCs) could be activated repeatedly by 18 F-FDG and exhibited long-lasting luminescence after excitation, allowing for in vivo imaging with high sensitivity and long decay time. 478 (Ba 0.55 Y 0.3 F 2 :Eu 3+ ) that could be excited by 18 F-FDG for in vivo imaging. 539 The use of Cherenkov radiation for effective energy transfer between fluorophores and radionuclides requires close proximity due to the strong absorption of Cherenkov radiation by biological tissues.…”
Section: Cerenkov Luminescence Imagingmentioning
confidence: 99%
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“…For example, Cheng et al discovered that ZnGa 2 O 4 :Cr 3+ (ZGCs) could be activated repeatedly by 18 F-FDG and exhibited long-lasting luminescence after excitation, allowing for in vivo imaging with high sensitivity and long decay time. 478 (Ba 0.55 Y 0.3 F 2 :Eu 3+ ) that could be excited by 18 F-FDG for in vivo imaging. 539 The use of Cherenkov radiation for effective energy transfer between fluorophores and radionuclides requires close proximity due to the strong absorption of Cherenkov radiation by biological tissues.…”
Section: Cerenkov Luminescence Imagingmentioning
confidence: 99%
“…538 18 Ffluorodeoxyglucose ( 18 F-FDG) is a clinically approved radiopharmaceutical used for tumor imaging, which has a short halflife of approximately 110 min. Cherenkov luminescence imaging using 18 F-FDG as the light source enables deep-tissue in vivo imaging. For example, Cheng et al discovered that ZnGa 2 O 4 :Cr 3+ (ZGCs) could be activated repeatedly by 18 F-FDG and exhibited long-lasting luminescence after excitation, allowing for in vivo imaging with high sensitivity and long decay time.…”
Section: Cerenkov Luminescence Imagingmentioning
confidence: 99%
See 1 more Smart Citation
“…Currently, MRI-based breast cancer screening is highly valued by clinicians and researchers [10,11,12,13,14]. Typically, only T1-weighted pre-and post-contrast MRI and DWI or T2 are included in the screening protocols, and while some abbreviated MRI protocols have also explored obtaining more MRI parameters, this is time-consuming and costly [3,15,16,17,18]. Unfortunately, this may lead to missing characteristic information of unscanned MRI sequences, such as T2-weighted MRI, that may sometimes be valuable for breast lesion characterization [19,3,20].…”
Section: Introductionmentioning
confidence: 99%
“…[1] For women with high risk of breast cancer, magnetic resonance imaging (MRI) has been proven to be an important tool for the examination of suspicious breast lesions, [2] as MRI provides multi-directional and multi-sequence imaging along with high soft tissue discrimination ability and can define the nature of the lesions through the blood supply situation around the mass. [3] More importantly, as a functional method of imaging, MRI can reflect the diffusion of water molecules in living tissues by the apparent diffusion coefficient (ADC). Diffusion-weighted imaging (DWI) has been widely used for diagnosis, prognosis, efficacy monitoring and evaluation of recurrence and metastasis.…”
Section: Introductionmentioning
confidence: 99%