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Apparent diffusion coefficient in pancreatic cancer: Characterization and histopathological correlations
Author(s) -
Muraoka Noriaki,
Uematsu Hidemasa,
Kimura Hirohiko,
Imamura Yoshiaki,
Fujiwara Yasuhiro,
Murakami Makoto,
Yamaguchi Akio,
Itoh Harumi
Publication year - 2008
Publication title -
journal of magnetic resonance imaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.563
H-Index - 160
eISSN - 1522-2586
pISSN - 1053-1807
DOI - 10.1002/jmri.21340
Subject(s) - effective diffusion coefficient , pancreatic cancer , fibrosis , medicine , diffusion mri , pathology , nuclear medicine , cancer , necrosis , magnetic resonance imaging , radiology
Purpose To clarify the components primarily responsible for diffusion abnormalities in pancreatic cancerous tissue. Materials and Methods Subjects comprised 10 patients with surgically confirmed pancreatic cancer. Diffusion‐weighted (DW) echo‐planar imaging (b value = 0, 500 s/mm 2 ) was employed to calculate the apparent diffusion coefficient (ADC). ADC values of cancer and noncancerous tissue were calculated. Furthermore, ADC values of the cancer were compared with histopathological results. Results The mean (±standard deviation) ADC value was significantly lower for tumor (1.27 ± 0.52 × 10 −3 mm 2 /s) than for noncancerous tissue (1.90 ± 0.41 × 10 −3 mm 2 /s, P < 0.05). Histopathological examination showed similar proportions of fibrotic area, cellular component, necrosis, and mucin in each case. Regarding the density of fibrosis in cancer, three cases were classified in the loose fibrosis group and the remaining seven cases were classified in the dense fibrosis group. The mean ADC value was significantly higher in the loose fibrosis group (1.88 ± 0.39 × 10 −3 mm 2 /s) than in the dense fibrosis group (1.01 ± 0.29 × 10 −3 mm 2 /s, P < 0.05). In quantitative analysis, ADC correlated well with the proportion of collagenous fibers ( r = −0.87, P < 0.05). Conclusion Collagenous fibers may be responsible for diffusion abnormalities in pancreatic cancer. J. Magn. Reson. Imaging 2008;27:1302–1308. © 2008 Wiley‐Liss, Inc.