TY - JOUR
T1 - Evaluation of diffusivity in pituitary adenoma
T2 - 3D turbo field echo with diffusion-sensitized drivenequilibrium preparation
AU - Hiwatashi, Akio
AU - Togao, Osamu
AU - Yamashita, Koji
AU - Kikuchi, Kazufumi
AU - Obara, Makoto
AU - Yoshiura, Takashi
AU - Honda, Hiroshi
N1 - Publisher Copyright:
© 2016 The Authors.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2016
Y1 - 2016
N2 - Objective: Diffusivity of pituitary adenoma has not been investigated fully. The purpose of this study was to evaluate the feasibility of turbo field echo with diffusion-sensitized driven-equilibrium (DSDE-TFE) preparation for pituitary adenoma in the sella turcica and unaffected anterior lobe of the pituitary gland. Methods: This retrospective study included 23 adult patients with pituitary adenomas. Among them, 6 each were prolactin-producing adenomas and growth hormoneproducing adenomas (GH) and the remaining 11 were non-functioning adenomas (NON). The apparent diffusion coefficients (ADCs) were measured in the pituitary adenoma and in the unaffected pituitary gland using coronal reformatted plane. Results: All pituitary adenomas were clearly visualized on DSDE-TFE and ADC maps without obvious geometrical distortion. There were no statistically significant differences in ADC of the all pituitary adenoma (1.506 0.61×10-3mm2 s-1) and the unaffected anterior lobe of the pituitary gland (1.49±0.37×10-3mm2 s-1, p=0.99). The ADC in prolactin-producing adenomas (2.04± 0.7×10-3mm2 s-1) was significantly higher than that in GH (1.26±0.47×10-3mm2 s-1; p<0.05) and NON (1.33±0.42×10-3mm2 s-1; p=0.04). There was no statistically significant difference between GH and NON (p=0.97). The intraclass correlation coefficient for ADC was 0.985 in adenomas and 0.635 in unaffected glands. Conclusion: With its insensitivity to field inhomogeneity and high spatial resolution, DSDE-TFE proved a feasible method for evaluating the diffusivity in the pituitary gland and adenoma. Advances in knowledge: DSDE-TFE could enable us to assess ADC of pituitary adenoma in the sella turcica with high resolution and few susceptibility artefacts.
AB - Objective: Diffusivity of pituitary adenoma has not been investigated fully. The purpose of this study was to evaluate the feasibility of turbo field echo with diffusion-sensitized driven-equilibrium (DSDE-TFE) preparation for pituitary adenoma in the sella turcica and unaffected anterior lobe of the pituitary gland. Methods: This retrospective study included 23 adult patients with pituitary adenomas. Among them, 6 each were prolactin-producing adenomas and growth hormoneproducing adenomas (GH) and the remaining 11 were non-functioning adenomas (NON). The apparent diffusion coefficients (ADCs) were measured in the pituitary adenoma and in the unaffected pituitary gland using coronal reformatted plane. Results: All pituitary adenomas were clearly visualized on DSDE-TFE and ADC maps without obvious geometrical distortion. There were no statistically significant differences in ADC of the all pituitary adenoma (1.506 0.61×10-3mm2 s-1) and the unaffected anterior lobe of the pituitary gland (1.49±0.37×10-3mm2 s-1, p=0.99). The ADC in prolactin-producing adenomas (2.04± 0.7×10-3mm2 s-1) was significantly higher than that in GH (1.26±0.47×10-3mm2 s-1; p<0.05) and NON (1.33±0.42×10-3mm2 s-1; p=0.04). There was no statistically significant difference between GH and NON (p=0.97). The intraclass correlation coefficient for ADC was 0.985 in adenomas and 0.635 in unaffected glands. Conclusion: With its insensitivity to field inhomogeneity and high spatial resolution, DSDE-TFE proved a feasible method for evaluating the diffusivity in the pituitary gland and adenoma. Advances in knowledge: DSDE-TFE could enable us to assess ADC of pituitary adenoma in the sella turcica with high resolution and few susceptibility artefacts.
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U2 - 10.1259/bjr.20150755
DO - 10.1259/bjr.20150755
M3 - Article
C2 - 27187598
AN - SCOPUS:84989306630
SN - 0007-1285
VL - 89
JO - British Journal of Radiology
JF - British Journal of Radiology
IS - 1063
M1 - 20150755
ER -