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Liver metastases: imaging considerations for protocol development with Multislice CT (MSCT)

Conventional, single-slice helical computed tomography (SSCT) allowed for scanning the majority of the liver during the critical portal venous phase. This was often referred to as the ‘optimal temporal window’. The introduction of current day multislice CT (MSCT) now allows us to acquire images in a...

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Autor principal: Silverman, Paul M
Formato: Texto
Lenguaje:English
Publicado: e-MED 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693768/
https://www.ncbi.nlm.nih.gov/pubmed/17098650
http://dx.doi.org/10.1102/1470-7330.2006.0024
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author Silverman, Paul M
author_facet Silverman, Paul M
author_sort Silverman, Paul M
collection PubMed
description Conventional, single-slice helical computed tomography (SSCT) allowed for scanning the majority of the liver during the critical portal venous phase. This was often referred to as the ‘optimal temporal window’. The introduction of current day multislice CT (MSCT) now allows us to acquire images in a much shorter time and more precisely than ever before. This yields increased conspicuity between low attenuation lesions and the enhanced normal liver parenchyma and optimal imaging for the vast majority of hepatic hypovascular metastases. Most importantly, these scanners, when compared to conventional non-helical scanners, avoid impinging upon the ‘equilibrium’ phase when tumors can become isodense/invisible. MSCT also allows for true multiphase scanning during the arterial and late arterial phases for detection of hypervascular metastases. The MSCT imaging speed has increased significantly over the past years with the introduction of 32- and 64-detector systems and will continue to increase in the future volumetric CT. This provides a number of important gains that are discussed in detail.
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spelling pubmed-16937682008-11-08 Liver metastases: imaging considerations for protocol development with Multislice CT (MSCT) Silverman, Paul M Cancer Imaging Article Conventional, single-slice helical computed tomography (SSCT) allowed for scanning the majority of the liver during the critical portal venous phase. This was often referred to as the ‘optimal temporal window’. The introduction of current day multislice CT (MSCT) now allows us to acquire images in a much shorter time and more precisely than ever before. This yields increased conspicuity between low attenuation lesions and the enhanced normal liver parenchyma and optimal imaging for the vast majority of hepatic hypovascular metastases. Most importantly, these scanners, when compared to conventional non-helical scanners, avoid impinging upon the ‘equilibrium’ phase when tumors can become isodense/invisible. MSCT also allows for true multiphase scanning during the arterial and late arterial phases for detection of hypervascular metastases. The MSCT imaging speed has increased significantly over the past years with the introduction of 32- and 64-detector systems and will continue to increase in the future volumetric CT. This provides a number of important gains that are discussed in detail. e-MED 2006-11-08 /pmc/articles/PMC1693768/ /pubmed/17098650 http://dx.doi.org/10.1102/1470-7330.2006.0024 Text en Copyright © 2006 International Cancer Imaging Society
spellingShingle Article
Silverman, Paul M
Liver metastases: imaging considerations for protocol development with Multislice CT (MSCT)
title Liver metastases: imaging considerations for protocol development with Multislice CT (MSCT)
title_full Liver metastases: imaging considerations for protocol development with Multislice CT (MSCT)
title_fullStr Liver metastases: imaging considerations for protocol development with Multislice CT (MSCT)
title_full_unstemmed Liver metastases: imaging considerations for protocol development with Multislice CT (MSCT)
title_short Liver metastases: imaging considerations for protocol development with Multislice CT (MSCT)
title_sort liver metastases: imaging considerations for protocol development with multislice ct (msct)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693768/
https://www.ncbi.nlm.nih.gov/pubmed/17098650
http://dx.doi.org/10.1102/1470-7330.2006.0024
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