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(Radiographics. 2000;20:1341-1352.)
© RSNA, 2000


SCIENTIFIC EXHIBIT

Contrast-enhanced Three-dimensional Fast Spoiled Gradient-Echo Renal MR Imaging: Evaluation of Vascular and Nonvascular Disease1

Steven G. Heiss, MD , Roger Y. Shifrin, MD and F. Graham Sommer, MD

1 From the Department of Radiology, Stanford University Medical Center, 300 Pasteur Dr, Rm H-1307, Stanford, CA 94305-5105. Presented as a scientific exhibit at the 1998 RSNA scientific assembly. Received September 9, 1999; revision requested November 5 and received December 2; accepted December 13. Address correspondence to F.G.S. (e-mail: gsommer@leland.stanford.edu).


    Abstract
 Top
 Abstract
 Introduction
 MR Imaging Technique
 Vascular Imaging
 Renal Infection
 Detection and Characterization...
 Renal Trauma
 Conclusions
 References
 
Breath-hold contrast materialenhanced three-dimensional (3D) fast spoiled gradient-echo (FSPGR) sequences are valuable techniques for evaluation of renal arteries and veins and diagnosis of significant renal arterial stenosis at magnetic resonance (MR) imaging. The excellent spatial and contrast resolution with these techniques, combined with the ability to perform studies in multiple vascular phases, also make them attractive for the diagnosis of a wide range of nonvascular processes that affect the kidneys, including renal infections, renal parenchymal diseases, and renal trauma. Particularly when combined with T1- and T2-weighted MR imaging, the contrast-enhanced techniques are highly effective for characterization of renal masses owing to the ability to portray dynamic contrast enhancement. The ability to display venous structures with contrast-enhanced 3D FSPGR techniques helps staging of renal cell carcinoma. This article presents examples of the wide range of vascular and nonvascular renal diseases that may be effectively imaged with contrast materialenhanced 3D FSPGR techniques and illustrates the usefulness of the techniques for renal MR imaging.

Index Terms: Kidney, infection, 81.20 • Kidney, injuries, 81.41 • Kidney, MR, 81.12143 • Kidney neoplasms, diagnosis, 81.30 • Magnetic resonance (MR), vascular studies, 961.12942 • Renal arteries, stenosis or obstruction, 961.122, 961.12942, 961.721


    Introduction
 Top
 Abstract
 Introduction
 MR Imaging Technique
 Vascular Imaging
 Renal Infection
 Detection and Characterization...
 Renal Trauma
 Conclusions
 References
 
Gadolinium-enhanced renal magnetic resonance (MR) imaging is attractive as an alternative to other techniques for evaluation of native and transplanted kidneys because it can be used in patients with renal failure or iodine allergies (1). In this study, we used a contrast materialenhanced three-dimensional (3D) fast spoiled gradient-echo (FSPGR) technique with radio-frequency and gradient spoiling. Although our sequence was customized to take advantage of the enhanced gradients of our MR imaging system (Signa; GE Medical Systems, Milwaukee, Wis), similar sequences for rapid contrast-enhanced 3D imaging are available with all current MR imaging systems.

Recent developments in 3D FSPGR sequences led to their increased usefulness for renal imaging (24). Multiphasic studies of the kidneys are possible during enhancement with gadolinium-based contrast material; both the renal arteries and veins and the renal parenchyma can be evaluated with high spatial and contrast resolution. Beyond the vascular imaging for which the sequences were originally designed, a new imaging dimension is now possible. The techniques are particularly valuable for imaging of the renal parenchyma (5) and evaluation of contrast enhancement in renal masses (611). An attractive feature of the sequences is that each of the sequential phases may be acquired in a breath-hold interval; thus; respiratory degradation is minimized. Also, with use of contemporary techniques to correctly determine the timing of administration of a bolus of contrast material, a single dose of gadolinium-based contrast material, 0.1 mmol per kilogram of body weight, can be used. Since a true 3D acquisition is used, a wide variety of effective display reformatting techniques, such as maximum intensity projection and volume rendering, can be used in addition to conventional display in the typical coronal acquisition plane.

We find the contrast-enhanced 3D FSPGR technique (3) valuable for a wide range of renal vascular and nonvascular applications.


    MR Imaging Technique
 Top
 Abstract
 Introduction
 MR Imaging Technique
 Vascular Imaging
 Renal Infection
 Detection and Characterization...
 Renal Trauma
 Conclusions
 References
 
In this study, all patients underwent MR imaging with a 1.5-T system with enhanced magnetic field gradients (gradient strength, 22 mT/m; gradient slew rate, 120 mT/m/msec). The contrast-enhanced 3D FSPGR sequence developed at our institution (3) was performed typically in a coronal plane with a 512 x 192 matrix, 3–4-mm section thickness, and 32 phase encodings with zero filling to produce 64 coronal sections. Other parameters include a flip angle of 25°, 0.5 signals acquired, and minimum repetition time of approximately 4.6 msec and echo time of 1.6 msec (3). These factors generally resulted in acquisition with an approximately 30-second breath hold. A precontrast acquisition was performed, and after the bolus of contrast material was administered, three acquisitions were generally performed sequentially, with time allowed for patient respiration between phases. In general, the torso phased array was used for data acquisition in the first vascular phase of the study, and the body coil was used for acquisition in subsequent phases.

Gadopentetate dimeglumine (Magnevist; Berlex Laboratories, Wayne, NJ) was administered, generally at a dose of 0.1 mmol/kg with a power injector at 2–3 mL/sec with a saline solution flush and imaging delay from 5 seconds in small children to 15 seconds in adults. Early in our experience, we performed a timing bolus injection to determine the appropriate delay time. Later, we found that estimation of the expected optimal delay produced equally good results, as long as multiple acquisitions were performed (generally three phases). Image reformatting was performed with a workstation (Sun; Sun Microsystems, Palo Alto, Calif) and commercially available software (advantage windows version 2.0; GE Medical Systems).


    Vascular Imaging
 Top
 Abstract
 Introduction
 MR Imaging Technique
 Vascular Imaging
 Renal Infection
 Detection and Characterization...
 Renal Trauma
 Conclusions
 References
 
The ability to perform a multiphasic study of the renal vasculature with high spatial resolution by using a contrast-enhanced 3D FSPGR sequence led to successful application of the technique to evaluation of native kidneys in renal transplant donors (2,12) and transplanted kidneys in recipients (13,14) (Figs 1, 2). Correlative studies show an accuracy with contrast-enhanced 3D FSPGR techniques similar to that with computed tomographic (CT) angiography for the evaluation of renal transplant donors (10). Evaluation of the renal parenchyma in normal and transplanted kidneys is facilitated with the multiphasic study, which clearly depicts the renal medulla and cortex in various phases, including precontrast, corticomedullary, and tubular nephrographic phases (Fig 3).



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Figure 1a.   Normal renal transplant vasculature in a healthy renal transplant donor. (a, b) Oblique sliding thin-slab maximum intensity projection images from contrast-enhanced 3D FSPGR imaging depict each renal artery. (c) Curved-planar reformatted image in a later phase shows normal renal veins. (d) Volume-rendered image shows the renal arteries.

 


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Figure 1b.   Normal renal transplant vasculature in a healthy renal transplant donor. (a, b) Oblique sliding thin-slab maximum intensity projection images from contrast-enhanced 3D FSPGR imaging depict each renal artery. (c) Curved-planar reformatted image in a later phase shows normal renal veins. (d) Volume-rendered image shows the renal arteries.

 


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Figure 1c.   Normal renal transplant vasculature in a healthy renal transplant donor. (a, b) Oblique sliding thin-slab maximum intensity projection images from contrast-enhanced 3D FSPGR imaging depict each renal artery. (c) Curved-planar reformatted image in a later phase shows normal renal veins. (d) Volume-rendered image shows the renal arteries.

 


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Figure 1d.   Normal renal transplant vasculature in a healthy renal transplant donor. (a, b) Oblique sliding thin-slab maximum intensity projection images from contrast-enhanced 3D FSPGR imaging depict each renal artery. (c) Curved-planar reformatted image in a later phase shows normal renal veins. (d) Volume-rendered image shows the renal arteries.

 


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Figure 2a.   Renal transplant vasculature in a 1-year-old renal transplant recipient. Full-thickness (a) and oblique sliding thin-slab (3-cm section thickness) (b) maximum intensity projection images from contrast-enhanced 3D FSPGR imaging show the renal artery.

 


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Figure 2b.   Renal transplant vasculature in a 1-year-old renal transplant recipient. Full-thickness (a) and oblique sliding thin-slab (3-cm section thickness) (b) maximum intensity projection images from contrast-enhanced 3D FSPGR imaging show the renal artery.

 


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Figure 3a.   Normal renal enhancement patterns in a patient with normal function and kidneys: Precontrast (a) and postcontrast corticomedullary phase (b) and tubular nephrographic phase (c) images from dynamic contrast-enhanced 3D FSPGR show normal renal enhancement.

 


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Figure 3b.   Normal renal enhancement patterns in a patient with normal function and kidneys: Precontrast (a) and postcontrast corticomedullary phase (b) and tubular nephrographic phase (c) images from dynamic contrast-enhanced 3D FSPGR show normal renal enhancement.

 


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Figure 3c.   Normal renal enhancement patterns in a patient with normal function and kidneys: Precontrast (a) and postcontrast corticomedullary phase (b) and tubular nephrographic phase (c) images from dynamic contrast-enhanced 3D FSPGR show normal renal enhancement.

 
Many recent studies illustrate the effectiveness of contrast-enhanced 3D FSPGR techniques in the diagnosis and grading of significant stenoses of either native or transplanted renal arteries (Fig 4) (1518). To optimally visualize renal arterial stenosis, we often reformat arterial phase images to create maximum intensity projection, oblique sliding thin-slab maximum intensity projection, and volume-rendered images (Figs 2, 4). We also found the contrast-enhanced 3D FSPGR images to be effective for the evaluation of arteriovenous fistulas and malformations and venous thrombosis. Rapid imaging during multiple vascular phases gave dynamic information similar to that obtained with CT angiography and generally allowed clear delineation of both arterial and venous vasculature (Fig 5). The dynamic nature of the contrast-enhanced 3D FSPGR study allows visualization of arterial processes that affect the kidneys and excellent depiction of renal infarction, which may be caused by such processes (19). Figure 6, for example, depicts a case of aortic dissection affecting the renal arteries; renal infarction is well demonstrated by the lack of contrast material enhancement.



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Figure 4a.   Atherosclerotic renal arterial stenosis (50% diameter) is seen on the coronal contrast-enhanced 3D FSPGR source MR image (a), oblique sliding thin-slab maximum intensity projection image (b), and selective digital subtraction angiogram obtained prior to angioplasty (c).

 


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Figure 4b.   Atherosclerotic renal arterial stenosis (50% diameter) is seen on the coronal contrast-enhanced 3D FSPGR source MR image (a), oblique sliding thin-slab maximum intensity projection image (b), and selective digital subtraction angiogram obtained prior to angioplasty (c).

 


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Figure 4c.   Atherosclerotic renal arterial stenosis (50% diameter) is seen on the coronal contrast-enhanced 3D FSPGR source MR image (a), oblique sliding thin-slab maximum intensity projection image (b), and selective digital subtraction angiogram obtained prior to angioplasty (c).

 


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Figure 5a.   Renal arterial venous malformation. Oblique sliding thin-slab maximum intensity projection (a) and arterial phase curved-planar (b) reformatted images from contrast-enhanced 3D FSPGR imaging depict tortuous arterial branches and prominent early enhancement of the right renal vein.

 


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Figure 5b.   Renal arterial venous malformation. Oblique sliding thin-slab maximum intensity projection (a) and arterial phase curved-planar (b) reformatted images from contrast-enhanced 3D FSPGR imaging depict tortuous arterial branches and prominent early enhancement of the right renal vein.

 


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Figure 6.   Aortic dissection affecting renal arteries. Delayed contrast-enhanced 3D FSPGR MR image depicts aortic dissection extending into the left renal artery. A large portion of the left kidney (arrow) is not enhanced, consistent with infarction.

 
Vascular complications of renal allografts can also be demonstrated with the contrast-enhanced 3D FSPGR technique (20); both arterial stenosis (Fig 4) and renal transplant venous thrombosis can be diagnosed (Fig 7) on the basis of the multiphasic nature of the study.



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Figure 7a.   Renal transplant venous thrombosis. Contrast-enhanced 3D FSPGR images clearly show the main transplant artery (a) and several branches (b) in the left iliac fossa. (c) On delayed phase image, the transplant kidney is not enhanced, consistent with infarction.

 


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Figure 7b.   Renal transplant venous thrombosis. Contrast-enhanced 3D FSPGR images clearly show the main transplant artery (a) and several branches (b) in the left iliac fossa. (c) On delayed phase image, the transplant kidney is not enhanced, consistent with infarction.

 


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Figure 7c.   Renal transplant venous thrombosis. Contrast-enhanced 3D FSPGR images clearly show the main transplant artery (a) and several branches (b) in the left iliac fossa. (c) On delayed phase image, the transplant kidney is not enhanced, consistent with infarction.

 

    Renal Infection
 Top
 Abstract
 Introduction
 MR Imaging Technique
 Vascular Imaging
 Renal Infection
 Detection and Characterization...
 Renal Trauma
 Conclusions
 References
 
Contrast-enhanced 3D FSPGR sequences are very effective for the evaluation of renal infectious processes, including pyelonephritis (21), renal abscess, and perinephric inflammatory processes. The high sensitivity to contrast enhancement helps clear depiction of the segmental perfusion changes seen with pyelonephritis or any renal or perirenal fluid collections (Figs 8, 9). Additionally, contrast-enhanced 3D FSPGR techniques are effective for the evaluation of perfused renal parenchyma that remains after renal atrophy due to either obstruction or reflux nephropathy (Fig 10). Preliminary findings in renal obstructive disease indicate that study of the dynamic passage of gadolinium-based contrast material through the kidneys and the dilated collecting systems may help evaluate the degree of obstruction in a manner similar to that currently available with dynamic radionuclide scanning (22).



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Figure 8a.   Acute pyelonephritis depicted with contrast-enhanced 3D FSPGR imaging. (a) Precontrast MR image. (b) On early corticomedullary phase MR image, striated enhancement of the right kidney is prominent. (c) On 5-minute delayed image, the enhancement pattern is still abnormal, which helps confirm bilateral excretion of gadopentetate dimeglumine. The nonenhancing fluid (arrow) medial to the lower pole of the right kidney, which is evident in b and c, may represent a perinephric abscess, but a sterile urinoma could have an identical appearance.

 


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Figure 8b.   Acute pyelonephritis depicted with contrast-enhanced 3D FSPGR imaging. (a) Precontrast MR image. (b) On early corticomedullary phase MR image, striated enhancement of the right kidney is prominent. (c) On 5-minute delayed image, the enhancement pattern is still abnormal, which helps confirm bilateral excretion of gadopentetate dimeglumine. The nonenhancing fluid (arrow) medial to the lower pole of the right kidney, which is evident in b and c, may represent a perinephric abscess, but a sterile urinoma could have an identical appearance.

 


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Figure 8c.   Acute pyelonephritis depicted with contrast-enhanced 3D FSPGR imaging. (a) Precontrast MR image. (b) On early corticomedullary phase MR image, striated enhancement of the right kidney is prominent. (c) On 5-minute delayed image, the enhancement pattern is still abnormal, which helps confirm bilateral excretion of gadopentetate dimeglumine. The nonenhancing fluid (arrow) medial to the lower pole of the right kidney, which is evident in b and c, may represent a perinephric abscess, but a sterile urinoma could have an identical appearance.

 


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Figure 9a.   Psoas abscess. (a) Axial T2-weighted MR image depicts renal and perinephric inflammation, which extends to the left psoas muscle, as an ill-defined area of increased signal intensity. (b) Contrast-enhanced 3D FSPGR MR image demonstrates enhancement of corresponding regions of infection in the left kidney and left psoas muscle. A simple cyst is present in the upper pole of the right kidney.

 


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Figure 9b.   Psoas abscess. (a) Axial T2-weighted MR image depicts renal and perinephric inflammation, which extends to the left psoas muscle, as an ill-defined area of increased signal intensity. (b) Contrast-enhanced 3D FSPGR MR image demonstrates enhancement of corresponding regions of infection in the left kidney and left psoas muscle. A simple cyst is present in the upper pole of the right kidney.

 


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Figure 10a.   Reflux nephropathy depicted with contrast-enhanced 3D FSPGR imaging. (a) Corticomedullary phase image depicts a small left kidney with a striated enhancement pattern. (b) On the tubular nephrographic phase image, the areas of scarring and cortical thinning are depicted clearly.

 


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Figure 10b.   Reflux nephropathy depicted with contrast-enhanced 3D FSPGR imaging. (a) Corticomedullary phase image depicts a small left kidney with a striated enhancement pattern. (b) On the tubular nephrographic phase image, the areas of scarring and cortical thinning are depicted clearly.

 

    Detection and Characterization of Renal Masses
 Top
 Abstract
 Introduction
 MR Imaging Technique
 Vascular Imaging
 Renal Infection
 Detection and Characterization...
 Renal Trauma
 Conclusions
 References
 
Effectiveness of the contrast-enhanced 3D FSPGR sequences in detection and characterization of renal masses is evaluated in a number of studies (2,9,11,23,24); in some, the accuracy is comparable or slightly superior to that with contrast-enhanced CT (10). The accuracy may be a result of the high sensitivity to contrast enhancement through multiple phases and the ability to acquire images with high spatial resolution in all three planes. Contrast-enhanced 3D FSPGR MR imaging is accurate in the differentiation of simple cysts from complex cysts containing malignancy: Mural irregularity and intense mural enhancement are indicators of malignancy (6), whereas simple cysts were completely avascular (Fig 9a). The characteristic appearance of multilocular cystic nephroma is as a complex cystic renal lesion, often with enhancing septa and herniation of the lesion into the renal collecting system (7) (Fig 11). Contrast-enhanced 3D FSPGR MR images can depict the cystic changes in kidneys involved with autosomal dominant polycystic kidney disease (Fig 12) and delineate the perfused functional renal tissue that remains.



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Figure 11a.   Multilocular cystic nephroma depicted with contrast-enhanced 3D FSPGR imaging. (a) Corticomedullary phase image reveals a septated cystic mass in the left kidney. (b) Delayed image reveals that the left renal cystic lesion involves the renal sinus and displaces the renal pelvis, in a manner characteristic of multilocular cystic nephroma, with some enhancement in the septations (arrow).

 


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Figure 11b.   Multilocular cystic nephroma depicted with contrast-enhanced 3D FSPGR imaging. (a) Corticomedullary phase image reveals a septated cystic mass in the left kidney. (b) Delayed image reveals that the left renal cystic lesion involves the renal sinus and displaces the renal pelvis, in a manner characteristic of multilocular cystic nephroma, with some enhancement in the septations (arrow).

 


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Figure 12a.   Autosomal dominant polycystic kidney disease. (a) Contrast-enhanced 3D FSPGR MR image depicts several cysts with internal hemorrhage as hyperintense. (b) Fat-saturated fast spin-echo T2-weighted MR image depicts the cysts as iso- or hypointense. In a, the high spatial resolution, contrast sensitivity, and breath-hold technique allow evaluation of the intervening solid renal parenchyma and clearly define the nonenhancing cysts.

 


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Figure 12b.   Autosomal dominant polycystic kidney disease. (a) Contrast-enhanced 3D FSPGR MR image depicts several cysts with internal hemorrhage as hyperintense. (b) Fat-saturated fast spin-echo T2-weighted MR image depicts the cysts as iso- or hypointense. In a, the high spatial resolution, contrast sensitivity, and breath-hold technique allow evaluation of the intervening solid renal parenchyma and clearly define the nonenhancing cysts.

 
Contrast-enhanced 3D FSPGR MR images are particularly useful when combined with T1- and T2-weighted MR images, which provide additional information about cyst hemorrhage (2). Recent studies of contrast-enhanced 3D FSPGR MR imaging demonstrate an accuracy in the detection and characterization of renal cell carcinoma comparable to that with contrast-enhanced CT (Fig 13). Additionally, the ability to image the renal veins effectively in a multiphasic study allows accurate determination of renal vein and inferior vena caval involvement with renal cell carcinoma (Fig 14), which leads to an accuracy for staging of renal cell carcinoma somewhat higher than that with CT (25). Direct visualization of the renal arterial vasculature may help surgical planning of nephrectomy. By supplementing contrast-enhanced 3D FSPGR MR images with standard T1- and T2-weighted MR images, including those obtained with fat-sensitive sequences, the usefulness of the technique in the characterization of masses may be optimized (2,9). For example, such a technique may help detection of fat in an angiomyolipoma or vascularization of a mass on the contrast-enhanced 3D FSPGR MR images (Fig 15).



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Figure 13a.   Renal cell carcinoma. Fat-saturated fast spin-echo T2-weighted (a) and contrast-enhanced 3D FSPGR (b) MR images reveal a solid left renal mass. In b, the mass, arteries, and veins can be simultaneously evaluated. (c) Curved-planar image reformatted from b shows that the mass (arrow) involves the renal vein at only the renal hilum.

 


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Figure 13b.   Renal cell carcinoma. Fat-saturated fast spin-echo T2-weighted (a) and contrast-enhanced 3D FSPGR (b) MR images reveal a solid left renal mass. In b, the mass, arteries, and veins can be simultaneously evaluated. (c) Curved-planar image reformatted from b shows that the mass (arrow) involves the renal vein at only the renal hilum.

 


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Figure 13c.   Renal cell carcinoma. Fat-saturated fast spin-echo T2-weighted (a) and contrast-enhanced 3D FSPGR (b) MR images reveal a solid left renal mass. In b, the mass, arteries, and veins can be simultaneously evaluated. (c) Curved-planar image reformatted from b shows that the mass (arrow) involves the renal vein at only the renal hilum.

 


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Figure 14a.   Renal cell carcinoma with renal vein and inferior vena caval invasion. Fat-saturated fast spin-echo T2-weighted (a), T1-weighted spin-echo (b), and contrast-enhanced 3D FSPGR (c, d) MR images reveal a solid right renal mass. In c and d, tumor extension (arrows in d) into the inferior vena cava enhances progressively, which can help differentiate between bland thrombus and tumor thrombus.

 


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Figure 14b.   Renal cell carcinoma with renal vein and inferior vena caval invasion. Fat-saturated fast spin-echo T2-weighted (a), T1-weighted spin-echo (b), and contrast-enhanced 3D FSPGR (c, d) MR images reveal a solid right renal mass. In c and d, tumor extension (arrows in d) into the inferior vena cava enhances progressively, which can help differentiate between bland thrombus and tumor thrombus.

 


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Figure 14c.   Renal cell carcinoma with renal vein and inferior vena caval invasion. Fat-saturated fast spin-echo T2-weighted (a), T1-weighted spin-echo (b), and contrast-enhanced 3D FSPGR (c, d) MR images reveal a solid right renal mass. In c and d, tumor extension (arrows in d) into the inferior vena cava enhances progressively, which can help differentiate between bland thrombus and tumor thrombus.

 


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Figure 14d.   Renal cell carcinoma with renal vein and inferior vena caval invasion. Fat-saturated fast spin-echo T2-weighted (a), T1-weighted spin-echo (b), and contrast-enhanced 3D FSPGR (c, d) MR images reveal a solid right renal mass. In c and d, tumor extension (arrows in d) into the inferior vena cava enhances progressively, which can help differentiate between bland thrombus and tumor thrombus.

 


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Figure 15a.   Angiomyolipoma. Fat-saturated fast spin-echo T2-weighted (a), T1-weighted spin-echo (b), and arterial (c) and delayed phase (d) contrast-enhanced 3D FSPGR MR images reveal a solid left renal mass. In a and b, the mass is isointense to fat, but a hemorrhagic cyst could have a similar appearance. In c and d, the mass (arrow) is seen to enhance.

 


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Figure 15b.   Angiomyolipoma. Fat-saturated fast spin-echo T2-weighted (a), T1-weighted spin-echo (b), and arterial (c) and delayed phase (d) contrast-enhanced 3D FSPGR MR images reveal a solid left renal mass. In a and b, the mass is isointense to fat, but a hemorrhagic cyst could have a similar appearance. In c and d, the mass (arrow) is seen to enhance.

 


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Figure 15c.   Angiomyolipoma. Fat-saturated fast spin-echo T2-weighted (a), T1-weighted spin-echo (b), and arterial (c) and delayed phase (d) contrast-enhanced 3D FSPGR MR images reveal a solid left renal mass. In a and b, the mass is isointense to fat, but a hemorrhagic cyst could have a similar appearance. In c and d, the mass (arrow) is seen to enhance.

 


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Figure 15d.   Angiomyolipoma. Fat-saturated fast spin-echo T2-weighted (a), T1-weighted spin-echo (b), and arterial (c) and delayed phase (d) contrast-enhanced 3D FSPGR MR images reveal a solid left renal mass. In a and b, the mass is isointense to fat, but a hemorrhagic cyst could have a similar appearance. In c and d, the mass (arrow) is seen to enhance.

 

    Renal Trauma
 Top
 Abstract
 Introduction
 MR Imaging Technique
 Vascular Imaging
 Renal Infection
 Detection and Characterization...
 Renal Trauma
 Conclusions
 References
 
Although the sequence is not widely used for the evaluation of traumatic injury to the kidneys, contrast-enhanced 3D FSPGR MR imaging can help determine whether renal perfusion and excretion are intact in patients in whom iodinated contrast material cannot be used (Fig 16). The rapidity with which the study can be performed, sensitivity of the kidney to contrast enhancement, and high spatial resolution make the technique a viable alternative to contrast-enhanced CT.



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Figure 16a.   Renal laceration from blunt trauma. (a) Axial fat-saturated fast spin-echo T2-weighted MR image reveals a hypointense right renal laceration. (b) Contrast-enhanced 3D FSPGR MR image reveals that enhancement in the right kidney is less than that in the left kidney. The region of hematoma is the nonenhanced focus (arrow) at the lateral lower pole. A small amount of fluid is also seen around the left kidney.

 


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Figure 16b.   Renal laceration from blunt trauma. (a) Axial fat-saturated fast spin-echo T2-weighted MR image reveals a hypointense right renal laceration. (b) Contrast-enhanced 3D FSPGR MR image reveals that enhancement in the right kidney is less than that in the left kidney. The region of hematoma is the nonenhanced focus (arrow) at the lateral lower pole. A small amount of fluid is also seen around the left kidney.

 

    Conclusions
 Top
 Abstract
 Introduction
 MR Imaging Technique
 Vascular Imaging
 Renal Infection
 Detection and Characterization...
 Renal Trauma
 Conclusions
 References
 
Contrast-enhanced 3D FSPGR sequences were primarily designed and initially evaluated to help visualize renal arterial vasculature and diagnose renal arterial stenosis; however, their increasingly widespread application demonstrates that such techniques can help diagnose a wide range of renal vascular and nonvascular disease processes. Further studies are needed to determine the range of processes and renal disorders that can be successfully diagnosed with these techniques. The power of the contrast-enhanced 3D FSPGR technique stems from the ability for combined imaging of both renal arterial and venous vasculature, as well as the high contrast and spatial resolution with which the renal parenchyma can be imaged in a single breath hold, without respiratory degradation. The maximum diagnostic power of contrast-enhanced 3D FSPGR MR imaging, particularly for the evaluation of renal masses, is achieved when the images are supplemented with standard T1- and T2-weighted MR images.


    Footnotes
 
See the commentary by Frager following this article.

Abbreviations: FSPGR = fast spoiled gradient-echo, 3D = three-dimensional


    References
 Top
 Abstract
 Introduction
 MR Imaging Technique
 Vascular Imaging
 Renal Infection
 Detection and Characterization...
 Renal Trauma
 Conclusions
 References
 

  1. Rofsky NM, Weinreb JC, Bosniak MA, Libes RB, Birnbaum BA. Renal lesion characterization with gadolinium-enhanced MR imaging: efficacy and safety in patients with renal insufficiency. Radiology 1991; 180:85-89.[Abstract/Free Full Text]
  2. Prince MR. Renal MR angiography: a comprehensive approach. J Magn Reson Imaging 1998; 8:511-516.[Medline]
  3. Alley MT, Shifrin RY, Pelc NJ, Herfkens RJ. Ultrafast contrast-enhanced three-dimensional MR angiography: state of the art. RadioGraphics 1998; 18:273-285.[Abstract]
  4. Hany TF, Leung DA, Pfammatter T, Debatin JF. Contrast-enhanced magnetic resonance angiography of the renal arteries: original investigation. Invest Radiol 1998; 33:653-659.[Medline]
  5. Kettritz U, Semelka RC, Brown ED, Sharp TJ, Lawing WL, Colindres RE. MR findings in diffuse renal parenchymal disease. J Magn Reson Imaging 1996; 6:136-144.[Medline]
  6. Balci NC, Semelka RC, Patt RH, et al. Complex renal cysts: findings on MR imaging. AJR Am J Roentgenol 1999; 172:1495-1500.[Abstract/Free Full Text]
  7. Kettritz U, Semelka RC, Siegelman ES, Shoenut JP, Mitchell DG. Multilocular cystic nephroma: MR imaging appearance with current techniques, including gadolinium enhancement. J Magn Reson Imaging 1996; 6:145-148.[Medline]
  8. Rominger MB, Kenney PJ, Morgan DE, Bernreuter WK, Listinsky JJ. Gadolinium-enhanced MR imaging of renal masses. RadioGraphics 1992; 12:1097-1118.[Abstract]
  9. Semelka RC, Hricak H, Stevens SK, Finegold R, Tomei E, Carroll PR. Combined gadolinium-enhanced and fat-saturation MR imaging of renal masses. Radiology 1991; 178:803-809.[Abstract/Free Full Text]
  10. Semelka RC, Shoenut JP, Kroeker MA, MacMahon RG, Greenberg HM. Renal lesions: controlled comparison between CT and 1.5-T MR imaging with nonenhanced and gadolinium-enhanced fat-suppressed spin-echo and breath-hold FLASH techniques. Radiology 1992; 182:425-430.[Abstract/Free Full Text]
  11. Yamashita Y, Miyazaki T, Hatanaka Y, Takahashi M. Dynamic MRI of small renal cell carcinoma. J Comput Assist Tomogr 1995; 19:759-765.[Medline]
  12. Low RN, Martinez AG, Steinberg SM, et al. Potential renal transplant donors: evaluation with gadolinium-enhanced MR angiography and MR urography. Radiology 1998; 207:165-172.[Abstract/Free Full Text]
  13. Szolar DH, Preidler K, Ebner F, et al. Functional magnetic resonance imaging of human renal allografts during the post-transplant period: preliminary observations. Magn Reson Imaging 1997; 15:727-735.[Medline]
  14. Nakashima R, Yamashita Y, Tomiguchi S, Tsuji A, Takahashi M. Functional evaluation of transplanted kidneys by Gd-DTPA enhanced turbo FLASH MR imaging. Radiat Med 1996; 14:251-256.[Medline]
  15. Bakker J, Beek FJ, Beutler JJ, et al. Renal artery stenosis and accessory renal arteries: accuracy of detection and visualization with gadolinium-enhanced breath-hold MR angiography. Radiology 1998; 207:497-504.[Abstract/Free Full Text]
  16. De Cobelli F, Vanzulli A, Sironi S, et al. Renal artery stenosis: evaluation with breath-hold, three-dimensional, dynamic, gadolinium-enhanced versus three-dimensional, phase-contrast MR angiography. Radiology 1997; 205:689-695.[Abstract/Free Full Text]
  17. Gilfeather M, Yoon HC, Siegelman ES, et al. Renal artery stenosis: evaluation with conventional angiography versus gadolinium-enhanced MR angiography. Radiology 1999; 210:367-372.[Abstract/Free Full Text]
  18. Prince MR, Schoenberg SO, Ward JS, Londy FJ, Wakefield TW, Stanley JC. Hemodynamically significant atherosclerotic renal artery stenosis: MR angiographic features. Radiology 1997; 205:128-136.[Abstract/Free Full Text]
  19. Kim SH, Park JH, Han JK, Han MC, Kim S, Lee JS. Infarction of the kidney: role of contrast enhanced MRI. J Comput Assist Tomogr 1992; 16:924-928.[Medline]
  20. Johnson DB, Lerner CA, Prince MR, et al. Gadolinium-enhanced magnetic resonance angiography of renal transplants. Magn Reson Imaging 1997; 15:13-20.[Medline]
  21. Pennington DJ, Lonergan GJ, Flack CE, Waguespack RL, Jackson CB. Experimental pyelonephritis in piglets: diagnosis with MR imaging. Radiology 1996; 201:199-205.[Abstract/Free Full Text]
  22. Fichtner J, Spielman D, Herfkens R, Boineau FG, Lewy JE, Shortliffe LM. Ultrafast contrast enhanced magnetic resonance imaging of congenital hydronephrosis in a rat model. J Urol 1994; 152:682-687.[Medline]
  23. Rofsky NM, Bosniak MA. MR imaging in the evaluation of small ( <=3.0 cm) renal masses. Magn Reson Imaging Clin N Am 1997; 5:67-81.[Medline]
  24. Semelka RC, Kelekis NL, Burdeny DA, Mitchell DG, Brown JJ, Siegelman ES. Renal lymphoma: demonstration by MR imaging. AJR Am J Roentgenol 1996; 166:823-827.[Abstract/Free Full Text]
  25. Semelka RC, Shoenut JP, Magro CM, Kroeker MA, MacMahon R, Greenberg HM. Renal cancer staging: comparison of contrast-enhanced CT and gadolinium-enhanced fat-suppressed spin-echo and gradient-echo MR imaging. J Magn Reson Imaging 1993; 3:597-602.[Medline]

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