## Abstract ## Purpose: To prospectively evaluate whether dose reduction and the application of a prebolus technique can effectively alleviate signal saturation effects in T1 dynamic contrast enhanced (T1‐DCE) magnetic resonance imaging (MRI) data in breast tumors and lead to increased diagnostic
Accelerated dynamic MR imaging with a parallel imaging technique for hypervascular hepatocellular carcinomas: Usefulness of a test bolus in examination and subtraction imaging
✍ Scribed by Nobuyuki Takahashi; Hiroshi Yoshioka; Masayuki Yamaguchi; Yukihisa Saida; Yuji Itai
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 636 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1053-1807
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✦ Synopsis
Abstract
Purpose
To assess the impact of the accelerated dynamic MR imaging (ADMRI) approach using parallel imaging for detecting hypervascular hepatocellular carcinomas (HCCs) and to evaluate the usefulness of a test bolus in examination and subtraction imaging in this setting.
Materials and Methods
Thirty patients with 135 HCCs underwent ADMRI using a two‐dimensional gradient‐recalled echo sequence with parallel imaging. Seventeen patients were evaluated without a test bolus and 13 patients with a test bolus. The detectability of HCCs was calculated between the groups with and without a test bolus. ADMRI was evaluated regarding the signal‐to‐noise ratio (SNR) of the lesion and the liver, the contrast‐to‐noise ratio (CNR) of the lesion vs. the liver, and the feasibility of subtraction images.
Results
ADMRI with and without a test bolus had almost equal sensitivity (92.5% and 92.6%). No significant difference was seen in the SNR of lesions and the CNR of lesions vs. livers between both groups. With a test bolus, ADMRI could depict the peak enhancement of nodules on the 2nd or 3rd dynamic phases and optimized the timing of peak lesion enhancement. Subtraction images could be obtained regarding minimal slice misregistration.
Conclusion
ADMRI had high detectability of HCCs with and without a test bolus. J. Magn. Reson. Imaging 2003;18:80–89. © 2003 Wiley‐Liss, Inc.
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