2000
DOI: 10.1148/radiology.216.1.r00jl26163
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Islet Cell Tumor of the Pancreas: Biphasic CT versus MR Imaging in Tumor Detection

Abstract: Biphasic (especially PVP) CT and MR imaging have similar effectiveness in the detection of islet cell tumors if fat-saturated T1-weighted and delayed enhanced T1-weighted MR imaging are included.

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Cited by 253 publications
(110 citation statements)
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“…In a comparison study between MRI and CT as well as angiography for detection of metastatic lesions, MRI was shown to be superior [31] . As with CT, multiphasic CE MRI is recommended, with fat-suppressed CE T1-weighted (T1W) imaging providing the best accuracy, with an area under the receiveroperating curve (AUROC) of 0.98 [32] . This has been corroborated by a more recent study by Herwick et al [33] .…”
Section: Magnetic Resonance Imagingmentioning
confidence: 99%
“…In a comparison study between MRI and CT as well as angiography for detection of metastatic lesions, MRI was shown to be superior [31] . As with CT, multiphasic CE MRI is recommended, with fat-suppressed CE T1-weighted (T1W) imaging providing the best accuracy, with an area under the receiveroperating curve (AUROC) of 0.98 [32] . This has been corroborated by a more recent study by Herwick et al [33] .…”
Section: Magnetic Resonance Imagingmentioning
confidence: 99%
“…An improvement in MRI technique is the use of diffusion weighted MRI (DWI-MRI) for abdominal imaging. DWI is an MRI technique that detects changes in the molecular diffusion of water in biologic tissues and the valuable role of DWI in the detection of pancreatic tumors has been reported in several studies (Figure 4a,4b & 5) [33][34][35][36].…”
Section: Mrimentioning
confidence: 99%
“…We believe, however, that their sensitivities are similar and exceed 80%. 8 CT and MRI have the advantage of the detection of small liver metastases although they may be difficult to identify on contrast-enhanced CT and gadoliniumenhanced MRI. 9 The use of liver-specific contrast agents such as mangafodipir-DPDP may improve their detection.…”
Section: Neuroendocrine Tumoursmentioning
confidence: 99%
“…3 Genetic studies have also defined new and clinically distinct endocrine neoplasia syndromes, for example: several familial paraganglioma syndromes resulting from mutations in the succinate dehydrogenase subunit genes [4][5][6] ; multiple endocrine neoplasia type 4, 7 and hyperparathyroidism-jaw tumour syndrome. 8 As a rule, genetic testing and interpretation of the results is easier in the autosomal dominant neoplasia syndromes, where one abnormal allele is sufficient for disease. In contrast, genetic testing in inherited metabolic syndromes (for example, congenital adrenal hyperplasia) is complex and less useful.…”
Section: Shern L Chew Consultant Physician and Professor Of Endocrinmentioning
confidence: 99%