Basic Study
Copyright ©The Author(s) 2015.
World J Radiol. Aug 28, 2015; 7(8): 212-219
Published online Aug 28, 2015. doi: 10.4329/wjr.v7.i8.212
Figure 1
Figure 1 The microspheres in scanning electron microscope with a magnification of 150 ×.
Figure 2
Figure 2 The gross appearance and fluoroscopy picture of DC bead (left), Hepasphere (middle), and our microsphere (right).
Figure 3
Figure 3 The angiography of hepatic artery (A) and splenic artery (B).
Figure 4
Figure 4 The liver perfusion scan after our microsphere, Embosphere, or Gelfoam embolization showing blood flow reduced areas (green to blue areas) over the periphery of liver.
Figure 5
Figure 5 Serial non-enhanced computed tomography scans of pig’s liver taken on 4, 12, and 25 d after the microsphere embolization showing its radiopaque characteristic and the gradual fade along with time (white arrow).
Figure 6
Figure 6 Microscopic findings of liver showing intraarterial embolization materials (black arrow) and intact peripheral liver lobules (black arrow heads) after Gelfoam (A), Embosphere (B), or our microsphere (C) embolization (H-E stain, original magnification × 40).
Figure 7
Figure 7 Gross appearance of spleen after Gelfoam (A), Embosphere (B), or our microsphere (C) embolization showing various degree of infarction over the distal end of spleen.
Figure 8
Figure 8 Microscopic findings of spleen showing intraarterial embolization materials (arrow heads) and periarterial reactions after Gelfoam (A), Embosphere (B), or our microsphere (C) embolization (H-E stain, original magnification × 40). Note the degrading Gelfoam and our microsphere and the intact Embosphere at 28 d after the embolization.