2013
DOI: 10.1016/j.mri.2013.01.003
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Diffusion-weighted imaging (DWI) of the spleen in patients with liver cirrhosis and portal hypertension

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Cited by 24 publications
(28 citation statements)
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“…Patients with liver fi-brosis usually develop portal hypertension, causing splenomegaly, which can result in increased heterogeneity of the spleen parenchyma on ADC maps as well as changes in water diffusion. 12 DW-MRI is a non-invasive technique of great usefulness in the detection and differentiation of pathological lesions in the whole body, including the abdomen. However, there are some limitations to this method.…”
Section: Discussionmentioning
confidence: 99%
“…Patients with liver fi-brosis usually develop portal hypertension, causing splenomegaly, which can result in increased heterogeneity of the spleen parenchyma on ADC maps as well as changes in water diffusion. 12 DW-MRI is a non-invasive technique of great usefulness in the detection and differentiation of pathological lesions in the whole body, including the abdomen. However, there are some limitations to this method.…”
Section: Discussionmentioning
confidence: 99%
“…Several authors have proposed to use the spleen as a reference organ for ADC measurements of liver parenchyma [29,62] in order to decrease variability of liver ADC measurements despite the fact that patients with cirrhosis and portal hypertension frequently suffer from splenomegaly (enlargement of the spleen) [63] . Klasen et al [63] demonstrated that patients with liver cirrhosis and portal hypertension had significantly higher spleen ADCs.…”
Section: Spleenmentioning
confidence: 99%
“…Klasen et al [63] demonstrated that patients with liver cirrhosis and portal hypertension had significantly higher spleen ADCs. Spleen T2-relaxation times are 79 ± 15 ms and 61 ± 9 ms at 1.5T and 3.0T respectively [50] and some studies [24,64] did use echo times significantly higher than the T2-relaxation time.…”
Section: Spleenmentioning
confidence: 99%
“…The technique may be useful in determining pathology in the liver (degree of cirrhosis/fibrosis), kidneys (lesion characterization, renal failure, pyelonephritis), pancreas (pancreatitis and pancreatic cancer), bowel (Crohn's disease), and uterus (endometriosis) [2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18] . In a recent meta-analysis, Li et al [19] has shown a potential future role for this type of sequence to assess for cancers within the liver.…”
Section: Introductionmentioning
confidence: 99%