Reduced Field-of-View Diffusion-Weighted Magnetic Resonance Imaging of the Pancreas: Comparison with Conventional Single-Shot Echo-Planar Imaging

被引:38
作者
Kim, Hyungjin [1 ,3 ]
Lee, Jeong Min [1 ,4 ]
Yoon, Jeong Hee [1 ]
Jang, Jin-Young [2 ]
Kim, Sun-Whe [2 ]
Ryu, Ji Kon [5 ]
Kannengiesser, Stephan [6 ]
Ha, Joon Koo [1 ,4 ]
Choi, Byung Ihn [1 ,4 ]
机构
[1] Seoul Natl Univ Hosp, Dept Radiol, Seoul 03080, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Surg, Seoul 03080, South Korea
[3] Air Force Educ & Training Command, Aerosp Med Grp, Jinju 52634, South Korea
[4] Seoul Natl Univ, Coll Med, Inst Radiat Med, Seoul 03080, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Internal Med, Div Gastroenterol, Seoul 03080, South Korea
[6] Siemens Healthcare, Erlangen, Germany
关键词
Reduced field-of-view; Image quality; Apparent diffusion coefficient; Diffusion-weighted imaging; Magnetic resonance imaging; Pancreas; INTRAVOXEL-INCOHERENT-MOTION; FORMING FOCAL PANCREATITIS; SPINAL-CORD; DIFFERENTIAL-DIAGNOSIS; OPTIC-NERVE; RESOLUTION; MRI; CANCER; CARCINOMA; EPI;
D O I
10.3348/kjr.2015.16.6.1216
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objective: To investigate the image quality (IQ) and apparent diffusion coefficient (ADC) of reduced field-of-view (FOV) diffusion-weighted imaging (DWI) of pancreas in comparison with full. FOV DWI. Materials and Methods: In this retrospective study, 2 readers independently performed qualitative analysis of full FOV DWI (FOV, 38 x 38 cm; b-value, 0 and 500 s/mm(2)) and reduced FOV DWI (FOV, 28 x 8.5 cm; b-value, 0 and 400 s/mm(2)). Both procedures were conducted with a two-dimensional spatially selective radiofrequency excitation pulse, in 102 patients with benign or malignant pancreatic diseases (mean size, 27.5 14.4 mm). The study parameters included 1) anatomic structure visualization, 2) lesion conspicuity, 3) artifacts, 4) IQ score, and 5) subjective clinical utility for confirming or excluding initially considered differential diagnosis on conventional imaging. Another reader performed quantitative ADC measurements of focal pancreatic lesions and parenchyma. WiLcoxon signed-rank test was used to compare qualitative scores and ADCs between DWI sequences. Mann Whitney U-test was used to compare ADCs between the lesions and parenchyma. Results: On qualitative analysis, reduced FOV DWI showed better anatomic structure visualization (2.76 +/- 0.79 at b = 0 s/mm(2) and 2.81 +/- 0.64 at b = 400 s/mm(2)), lesion conspicuity (3.11 +/- 0.99 at b = 0 s/mm(2) and 3.15 +/- 0.79 at b = 400 s/mm(2)), IQ score (8.51 +/- 2.05 at b = 0 s/mm(2) and 8.79 +/- 1.60 at b = 400 s/mm(2)), and higher clinical utility (3.41 +/- 0.64), as compared to full FOV DWI (anatomic structure, 2.18 +/- 0.59 at b = 0 s/mm(2) and 2.56 +/- 0.47 at b = 500 s/mm(2); lesion conspicuity, 2.55 1.07 at b = 0 s/mm(2) and 2.89 +/- 0.86 at b = 500 s/mm(2); IQ score, 7.13 +/- 1.83 at b = 0 s/mm(2) and 8.17 +/- 1.31 at b = 500 s/mm(2); clinical utility, 3.14 +/- 0.70) (p < 0.05). Artifacts were significantly improved on reduced FOV DWI (2.65 +/- 0.68) at b = 0 +/- s/mm(2) (full FOV DWI, 2.41 +/- 0.63) (p < 0.001). On quantitative analysis, there were no significant differences between the 2 DWI sequences in ADCs of various pancreatic Lesions and parenchyma (p > 0.05). ADCs of adenocarcinomas (1.061 x 10(-3) mm(2)/s +/- 0.133 at reduced FOV and 1.079 x 10(-3) mm(2)/s +/- 0.135 at full FOV) and neuroendocrine tumors (0.983 x 10(-3) mm(2)/s +/- 0.152 at reduced FOV and 1.004 x 10(-3) mm(2)/s +/- 0.153 at full FOV) were significantly lower than those of parenchyma (1.191 x 10(-3) me/s +/- 0.125 at reduced FOV and 1.218 x 10(-3) mm(2)/s +/- 0.103 at full FOV) (p < 0.05). Conclusion: Reduced FOV DWI of the pancreas provides better overall IQ including better anatomic detail, Lesion conspicuity and subjective clinical utility.
引用
收藏
页码:1216 / 1225
页数:10
相关论文
共 34 条
[1]   Angiographic imaging with 2D RF pulses [J].
Alley, MT ;
Pauly, JM ;
Sommer, FG ;
Pelc, NJ .
MAGNETIC RESONANCE IN MEDICINE, 1997, 37 (02) :260-267
[2]  
Anaye A, 2009, J PANCREAS, V10, P528
[3]   Clinical Evaluation of Reduced Field-of-View Diffusion-Weighted Imaging of the Cervical and Thoracic Spine and Spinal Cord [J].
Andre, J. B. ;
Zaharchuk, G. ;
Saritas, E. ;
Komakula, S. ;
Shankaranarayan, A. ;
Banerjee, S. ;
Rosenberg, J. ;
Nishimura, D. G. ;
Fischbein, N. J. .
AMERICAN JOURNAL OF NEURORADIOLOGY, 2012, 33 (10) :1860-1866
[4]  
Balci Numan Cem, 2009, Top Magn Reson Imaging, V20, P43, DOI 10.1097/RMR.0b013e3181b48667
[5]   Diffusion-Weighted Magnetic Resonance Imaging in the Upper Abdomen: Technical Issues and Clinical Applications [J].
Bittencourt, Leonardo K. ;
Matos, Celso ;
Coutinho, Antonio C., Jr. .
MAGNETIC RESONANCE IMAGING CLINICS OF NORTH AMERICA, 2011, 19 (01) :111-+
[6]   Signal characteristic and enhancement patterns of pancreatic adenocarcinoma: evaluation with dynamic gadolinium enhanced MRI [J].
Chandarana, H. ;
Babb, J. ;
Macari, M. .
CLINICAL RADIOLOGY, 2007, 62 (09) :876-883
[7]   Technical aspects of MR diffusion imaging of the body [J].
Dietrich, Olaf ;
Biffar, Andreas ;
Baur-Melnyk, Andrea ;
Reiser, Maximilian F. .
EUROPEAN JOURNAL OF RADIOLOGY, 2010, 76 (03) :314-322
[8]   Contiguous-Slice Zonally Oblique Multislice (CO-ZOOM) Diffusion Tensor Imaging: Examples of In Vivo Spinal Cord and Optic Nerve Applications [J].
Dowell, Nicholas G. ;
Jenkins, Thomas M. ;
Ciccarelli, Olga ;
Miller, David H. ;
Wheeler-Kingshott, Claudia A. M. .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2009, 29 (02) :454-460
[9]   Pancreatic Diffusion-Weighted Imaging (DWI): Comparison Between Mass-Forming Focal Pancreatitis (FP), Pancreatic Cancer (PC), and Normal Pancreas [J].
Fattahi, Rana ;
Balci, N. Cem ;
Perman, William H. ;
Hsueh, Eddy C. ;
Alkaade, Samer ;
Havlioglu, Necat ;
Burton, Frank R. .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2009, 29 (02) :350-356
[10]   Diffusion-Weighted Imaging in the Differential Diagnosis of Cystic Lesions of the Pancreas [J].
Inan, Nagihan ;
Arslan, Arzu ;
Akansel, Gur ;
Anik, Yonca ;
Demirci, Ali .
AMERICAN JOURNAL OF ROENTGENOLOGY, 2008, 191 (04) :1115-1121