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Contrast enhancement of intracranial lesions at 1.5 T: comparison among 2D spin echo, black-blood (BB) Cube, and BB Cube-FLAIR sequences.

Authors :
Im S
Ashikaga R
Yagyu Y
Wakayama T
Miyoshi M
Hyodo T
Imaoka I
Kumano S
Ishii K
Murakami T
Source :
European radiology [Eur Radiol] 2015 Nov; Vol. 25 (11), pp. 3175-86. Date of Electronic Publication: 2015 May 01.
Publication Year :
2015

Abstract

Objectives: The purpose of this study was to investigate the usefulness of T1W black-blood Cube (BB Cube) and T1W BB Cube fluid-attenuated inversion recovery (BB Cube-FLAIR) sequences for contrast-enhanced brain imaging, by evaluating flow-related artefacts, detectability, and contrast ratio (CR) of intracranial lesions among these sequences and T1W-SE.<br />Methods: Phantom studies were performed to determine the optimal parameters of BB Cube and BB Cube-FLAIR. A clinical study in 23 patients with intracranial lesions was performed to evaluate the usefulness of these two sequences for the diagnosis of intracranial lesions compared with the conventional 2D T1W-SE sequence.<br />Results: The phantom study revealed that the optimal parameters for contrast-enhanced T1W imaging were TR/TE = 500 ms/minimum in BB Cube and TR/TE/TI = 600 ms/minimum/300 ms in BB Cube-FLAIR imaging. In the clinical study, the degree of flow-related artefacts was significantly lower in BB Cube and BB Cube-FLAIR than in T1W-SE. Regarding tumour detection, BB Cube showed the best detectability; however, there were no significant differences in CR among the sequences.<br />Conclusions: At 1.5 T, contrast-enhanced BB Cube was a better imaging sequence for detecting brain lesions than T1W-SE or BB Cube-FLAIR.<br />Key Points: • Cube is a single-slab 3D FSE imaging sequence. • We applied a black-blood (BB) imaging technique to T1W Cube. • At 1.5 T, contrast-enhanced T1W BB Cube was valuable for detecting brain lesions.

Details

Language :
English
ISSN :
1432-1084
Volume :
25
Issue :
11
Database :
MEDLINE
Journal :
European radiology
Publication Type :
Academic Journal
Accession number :
25929942
Full Text :
https://doi.org/10.1007/s00330-015-3757-5