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1 neuroendocrine tumors, which are known to be hypervascular.
3 es typically were irregular, hypoechoic, and hypervascular and demonstrated indistinct margins or an
5 ts with advanced hepatocellular carcinoma, a hypervascular and VEGF-rich tumor type, were treated wit
6 ncreatitis showed in the majority of cases a hypervascular appearance in the early arterial phase of
8 Clear cell RCCs and oncocytomas tended to be hypervascular, chromophobe lesions and angiomyolipomas t
9 hat recapitulates the extensive invasive and hypervascular features of glioblastoma (GBM) is a major
11 sociated architectural distortion) and has a hypervascular, hemorrhagic, and heterogeneous appearance
12 endothelial growth factor (VEGF)-transfected hypervascular human melanoma xenografts and their nontra
14 CT scan of the abdomen confirmed multiple hypervascular lesions and central areas of necrosis with
15 ry endolymphatic sac tumors are destructive, hypervascular lesions that arise from the temporal bone
17 ely evaluate, for the depiction of simulated hypervascular liver lesions in a phantom, the effect of
19 with various iodinated solutions to simulate hypervascular liver lesions was scanned with a 64-sectio
20 etection of statistically significantly more hypervascular liver metastases than do HAP plus PVP imag
22 n; age range, 35-77 years) with 60 malignant hypervascular liver tumors (mean diameter, 20.1 mm +/- 1
23 hnique improves the conspicuity of malignant hypervascular liver tumors during the late hepatic arter
24 nge, 51-77 years) known or suspected to have hypervascular liver tumors underwent dual-energy 64-sect
29 imaging cirrhosis is the characterization of hypervascular nodules smaller than 2 cm, which often hav
32 nts with biopsy-proved liver metastases from hypervascular primary tumors other than hepatocellular c
34 ted with a mixed enhancement pattern of both hypervascular soft-tissue components and low-attenuation
39 and 1.7-fold higher oxygen saturation in the hypervascular tumors as compared with the control tumor
40 -Lindau (VHL) develop renal cell cancers and hypervascular tumors of the brain, adrenal glands, and p
41 nt for inoperable hepatic tumors, especially hypervascular tumors such as hepatocellular carcinoma.
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