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1.
Radiographics ; 39(3): 690-708, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31059393

RESUMO

The US Liver Imaging Reporting and Data System (LI-RADS) was released in 2017 and is the newest of the four American College of Radiology (ACR) LI-RADS algorithms. US LI-RADS provides standardized terminology, technical recommendations, and a reporting framework for US examinations performed for screening or surveillance in patients at risk for developing hepatocellular carcinoma (HCC). The appropriate patient population for screening and surveillance includes individuals who are at risk for developing HCC but do not have known or suspected cancer. This includes patients with cirrhosis from any cause and subsets of patients with chronic hepatitis B virus infection in the absence of cirrhosis. In an HCC screening or surveillance study, US LI-RADS recommends assigning two scores that apply to the entire study: the US category, which determines follow-up, and a visualization score, which communicates the expected level of sensitivity of the examination but does not affect management. Three US categories are possible: US-1 negative, a study with no evidence of HCC; US-2 subthreshold, a study in which an observation less than 10 mm is depicted that is not definitely benign; and US-3 positive, a study in which an observation greater than or equal to 10 mm or a new thrombus in vein is identified, for which diagnostic contrast material-enhanced imaging is recommended. Three visualization scores are possible: A (no or minimal limitations), B (moderate limitations), and C (severe limitations). ©RSNA, 2019.


Assuntos
Algoritmos , Sistemas de Dados , Hepatopatias/diagnóstico por imagem , Fígado/diagnóstico por imagem , Ultrassonografia , Idoso , Carcinoma Hepatocelular/diagnóstico por imagem , Carcinoma Hepatocelular/patologia , Carcinoma Hepatocelular/prevenção & controle , Detecção Precoce de Câncer , Feminino , Humanos , Hepatopatias/classificação , Hepatopatias/patologia , Neoplasias Hepáticas/diagnóstico por imagem , Neoplasias Hepáticas/patologia , Neoplasias Hepáticas/prevenção & controle , Masculino , Pessoa de Meia-Idade , Vigilância da População , Ultrassonografia/instrumentação , Ultrassonografia/métodos
2.
Radiol Clin North Am ; 41(4): 695-708, 2003 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12899486

RESUMO

The value of all noninvasive prenatal tests must be viewed with the perspective of the consequences of invasive testing. Regarding second trimester noninvasive testing, biochemical screening is more accurate in establishing risk than maternal age alone. One or more major ultrasound abnormalities, nuchal thickening, or a shortened humerus should raise concern for Down syndrome regardless of the patient's a priori risk based on age or biochemical markers. Isolated minor ultrasound markers should not be used in calculating risk in low-risk patients regarding Down syndrome unless the biochemical profile already places the patient at risk or in a borderline risk zone. If the ultrasound finding is hyperechoic bowel, problems other than aneuploidy may be the cause, including cystic fibrosis, infection, or hemorrhage, and these problems must be considered if hyperechoic bowel is an isolated finding. Improved risk adjustment seems to be applicable to a priori high-risk patients with completely normal sonograms. Genetic sonograms with specific risk adjustment schemata may be used to adjust a priori risk (either maternal age or biochemical screening results) at centers in which this has proven to be accurate, but whether this is statistically sound remains to be determined. The goal of second trimester ultrasound screening is to identify at-risk fetuses better and offer invasive testing to a more select group of patients. As the value of first trimester screening becomes more evident and practical, and if the risk of chorionic villus sampling becomes an acceptable norm, the patient population that reaches the second trimester of pregnancy will be select. Therefore, we can anticipate that second trimester screening and invasive testing may be needed only in a minority of cases, and the practice standards of prenatal testing and sonography (including minor ultrasound markers) will change entirely.


Assuntos
Aneuploidia , Transtornos Cromossômicos/diagnóstico por imagem , Ultrassonografia Pré-Natal , Amniocentese , Amostra da Vilosidade Coriônica , Transtornos Cromossômicos/sangue , Transtornos Cromossômicos/diagnóstico , Cromossomos Humanos Par 13/genética , Cromossomos Humanos Par 18/genética , Cromossomos Humanos Par 21/genética , Cordocentese , Feminino , Humanos , Gravidez , Primeiro Trimestre da Gravidez/sangue , Primeiro Trimestre da Gravidez/genética , Segundo Trimestre da Gravidez/sangue , Segundo Trimestre da Gravidez/genética , Trissomia/diagnóstico
3.
Ultrasound Q ; 26(2): 83-99, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20498564

RESUMO

Doppler ultrasound is routinely used in the clinical setting to evaluate blood flow in many major vessels of the body. Spectral Doppler is used to display the normal and abnormal signature waveforms that are unique to each vessel. It is important for the sonographer and the radiologist to recognize both what is normal and what is abnormal in a spectral Doppler display. In this review, we briefly explain the physics behind Doppler ultrasound and some of the most common mathematical equations applied in a routine clinical examination. We also describe and demonstrate normal versus abnormal spectral Doppler signature waveforms of vessels in the neck, abdomen, pelvis, and fetus.


Assuntos
Vasos Sanguíneos/diagnóstico por imagem , Ultrassonografia Doppler em Cores/métodos , Ultrassonografia de Intervenção/métodos , Abdome/irrigação sanguínea , Abdome/diagnóstico por imagem , Aorta Abdominal/diagnóstico por imagem , Velocidade do Fluxo Sanguíneo/fisiologia , Artérias Carótidas/diagnóstico por imagem , Feminino , Humanos , Rim/irrigação sanguínea , Rim/diagnóstico por imagem , Masculino , Artéria Mesentérica Superior/diagnóstico por imagem , Pelve/irrigação sanguínea , Pelve/diagnóstico por imagem , Fluxo Sanguíneo Regional/fisiologia , Sensibilidade e Especificidade , Útero/irrigação sanguínea , Útero/diagnóstico por imagem
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