J Korean Soc Magn Reson Med.  2011 Apr;15(1):22-31. 10.13104/jksmrm.2011.15.1.22.

Detection of Hepatic Lesion: Comparison of Free-Breathing and Respiratory-Triggered Diffusion-Weighted MR imaging on 1.5-T MR system

Affiliations
  • 1Department of Radiology, Ilsan Paik Hospital, Inje University College of Medicine, Korea. meditererian@hanmail.net

Abstract

PURPOSE
To compare free-breathing and respiratory-triggered diffusion-weighted imaging on 1.5-T MR system in the detection of hepatic lesions.
MATERIALS AND METHODS
This single-institution study was approved by our institutional review board. Forty-seven patients (mean 57.9 year; M:F = 25:22) underwent hepatic MR imaging on 1.5-T MR system using both free-breathing and respiratory-triggered diffusion-weighted imaging (DWI) at a single examination. Two radiologists retrospectively reviewed respiratory-triggered and free-breathing sets (B50, B400, B800 diffusion weighted images and ADC map) in random order with a time interval of 2 weeks. Liver SNR and lesion-to-liver CNR of DWI were calculated measuring ROI.
RESULTS
Total of 62 lesions (53 benign, 9 malignant) that included 32 cysts, 13 hemangiomas, 7 hepatocellular carcinomas (HCCs), 5 eosinophilic infiltration, 2 metastases, 1 eosinophilic abscess, focal nodular hyperplasia, and pseudolipoma of Glisson's capsule were reviewed by two reviewers. Though not reaching statistical significance, the overall lesion sensitivities were increased in respiratory-triggered DWI [reviewer1: reviewer2, 47/62(75.81%):45/62(72.58%)] than free-breathing DWI [44/62(70.97%):41/62(66.13%)]. Especially for smaller than 1 cm hepatic lesions, sensitivity of respiratory-triggered DWI [24/30(80%):21/30(70%)] was superior to free-breathing DWI [17/30(56.7%):15/30(50%)]. The diagnostic accuracy measuring the area under the ROC curve (Az value) of free-breathing and respiratory-triggered DWI was not statistically different. Liver SNR and lesion-to-liver CNR of respiratorytriggered DWI (87.6+/-41.4, 41.2+/-62.5) were higher than free-breathing DWI (38.8+/-13.6, 24.8+/-36.8) (p value <0.001, respectively).
CONCLUSION
Respiratory-triggered diffusion-weighted MR imaging seemed to be better than free-breathing diffusion-weighted MR imaging on 1.5-T MR system for the detection of smaller than 1 cm lesions by providing high SNR and CNR.

Keyword

Diffusion-weighted imaging; Magnetic resonance imaging (MRI); Liver; Single shot EPI

MeSH Terms

Abscess
Carcinoma, Hepatocellular
Diffusion
Eosinophils
Ethics Committees, Research
Focal Nodular Hyperplasia
Hemangioma
Humans
Liver
Neoplasm Metastasis
Retrospective Studies
ROC Curve

Figure

  • Fig. 1 64-year-old man with a tiny cyst. A 0.5 cm cyst (long arrow) was incidentally found during survey of hepatocellular carcinoma (not shown here). It was detected by two reviewers on respiratory-triggered DWI (e to h), but obscure on free-breathing DWI (a to d) and not detected. Note that the lesion was more depictive and brighter on respiratory-triggered DWI.

  • Fig. 2 52-year-old man with hepatocellular carcinoma. Both reviewers detected a 1.4 cm hepatocellular carcinoma (long arrow) on free-breathing DWI (a to d) and respiratory-triggered DWI (e to h). However the lesion demonstrated sharper margin and increased CNR on respiratory-triggered DWI. Note the high signals on high b value, representing water restriction. Enhanced dynamic study showed arterial enhancement and early washout (i). HCC had grown on short-term follow-up CT (j) and treated successfully with radiofrequency ablation. Note a tiny cyst (arrowhead) behind HCC.

  • Fig. 3 57-year-old man with common bile duct (CBD) stone. As well as increased depiction of liver edge and intrahepatic vessels, the edge of CBD was also increased, so a dark signal 0.6 cm sized stone (long arrow) was depicted finely on respiratory-triggered DWI (e to h) compared with free breathing DWI (a to d). It showed dense calcification on CT examination (i) and filling defect (large arrow) on MRCP (j). Note another small stone (arrowhead) in distal CBD on MRCP. Note sharp margin of right diaphragmatic crura (asterisk) on respiratory-triggered DWI.


Reference

1. Elsayes KM, Leyendecker JR, Menias CO, et al. MRI characterization of 124 CT-indeterminate focal hepatic lesions: evaluation of clinical utility. HPB (Oxford). 2007. 9:208–215.
2. Ward J. New MR techniques for the detection of liver metastases. Cancer Imaging. 2006. 6:33–42.
3. Muller MF, Prasad P, Siewert B, Nissenbaum MA, Raptopoulos V, Edelman RR. Abdominal diffusion mapping with use of a whole-body echo-planar system. Radiology. 1994. 190:475–478.
4. Ichikawa T, Haradome H, Hachiya J, Nitatori T, Araki T. Diffusion-weighted MR imaging with a single-shot echoplanar sequence: detection and characterization of focal hepatic lesions. AJR Am J Roentgenol. 1998. 170:397–402.
5. Namimoto T, Yamashita Y, Sumi S, Tang Y, Takahashi M. Focal liver masses: characterization with diffusion-weighted echo-planar MR imaging. Radiology. 1997. 204:739–744.
6. Vossen JA, Buijs M, Liapi E, Eng J, Bluemke DA, Kamel IR. Receiver operating characteristic analysis of diffusion-weighted magnetic resonance imaging in differentiating hepatic hemangioma from other hypervascular liver lesions. J Comput Assist Tomogr. 2008. 32:750–756.
7. Bruegel M, Holzapfel K, Gaa J, et al. Characterization of focal liver lesions by ADC measurements using a respiratory triggered diffusion-weighted single-shot echo-planar MR imaging technique. Eur Radiol. 2008. 18:477–485.
8. Kwee TC, Takahara T, Koh DM, Nievelstein RA, Luijten PR. Comparison and reproducibility of ADC measurements in breathhold, respiratory triggered, and free-breathing diffusion-weighted MR imaging of the liver. J Magn Reson Imaging. 2008. 28:1141–1148.
9. Nasu K, Kuroki Y, Sekiguchi R, Nawano S. The effect of simultaneous use of respiratory triggering in diffusion-weighted imaging of the liver. Magn Reson Med Sci. 2006. 5:129–136.
10. Gourtsoyianni S, Papanikolaou N, Yarmenitis S, Maris T, Karantanas A, Gourtsoyiannis N. Respiratory gated diffusion-weighted imaging of the liver: value of apparent diffusion coefficient measurements in the differentiation between most commonly encountered benign and malignant focal liver lesions. Eur Radiol. 2008. 18:486–492.
11. Kandpal H, Sharma R, Madhusudhan KS, Kapoor KS. Respiratory-triggered versus breath-hold diffusion-weighted MRI of liver lesions: comparison of image quality and apparent diffusion coefficient values. AJR Am J Roentgenol. 2009. 192:915–922.
12. Holzapfel K, Bruegel M, Eiber M, et al. Characterization of small (≤10mm) focal liver lesions: Value of respiratory-triggered echo-planar diffusion-weighted MR imaging. Eur J Radiol. 2009.
13. Quan XY, Sun XJ, Yu ZJ, Tang M. Evaluation of diffusion weighted imaging of magnetic resonance imaging in small focal hepatic lesions: a quantitative study in 56 cases. Hepatobiliary Pancreat Dis Int. 2005. 4:406–409.
14. Koh DM, Scurr E, Collins DJ, et al. Colorectal hepatic metastases: quantitative measurements using single-shot echo-planar diffusion-weighted MR imaging. Eur Radiol. 2006. 16:1898–1905.
15. Nasu K, Kuroki Y, Nawano S, et al. Hepatic metastases: diffusion-weighted sensitivity-encoding versus SPIO-enhanced MR imaging. Radiology. 2006. 239:122–130.
16. Xu PJ, Yan FH, Wang JH, Lin J, Ji Y. Added value of breathhold diffusion-weighted MRI in detection of small hepatocellular carcinoma lesions compared with dynamic contrast-enhanced MRI alone using receiver operating characteristic curve analysis. J Magn Reson Imaging. 2009. 29:341–349.
17. Bruegel M, Gaa J, Waldt S, et al. Diagnosis of hepatic metastasis: comparison of respiration-triggered diffusionweighted echo-planar MRI and five t2-weighted turbo spin-echo sequences. AJR Am J Roentgenol. 2008. 191:1421–1429.
18. Parikh T, Drew SJ, Lee VS, et al. Focal liver lesion detection and characterization with diffusion-weighted MR imaging: comparison with standard breath-hold T2-weighted imaging. Radiology. 2008. 246:812–822.
19. Nasu K, Kuroki Y, Fujii H, Minami M. Hepatic pseudo-anisotropy: a specific artifact in hepatic diffusion-weighted images obtained with respiratory triggering. MAGMA. 2007. 20:205–211.
20. Bruix J, Sherman M, Llovet JM, et al. Clinical management of hepatocellular carcinoma. Conclusions of the Barcelona-2000 EASL conference. European Association for the Study of the Liver. J Hepatol. 2001. 35:421–430.
21. Bruix J, Sherman M. Practice Guidelines Committee, American Association for the Study of Liver Diseases. Management of Hepatocellular carcinoma. Hepatology. 2005. 42:1208–1236.
Full Text Links
  • JKSMRM
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr