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AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

Review ArticleExtracranial Vascular
Open Access

Imaging Carotid Atherosclerosis Plaque Ulceration: Comparison of Advanced Imaging Modalities and Recent Developments

J. Yuan, A. Usman, T. Das, A.J. Patterson, J.H. Gillard and M.J. Graves
American Journal of Neuroradiology April 2017, 38 (4) 664-671; DOI: https://doi.org/10.3174/ajnr.A5026
J. Yuan
aFrom the Department of Radiology (J.Y., A.U., J.H.G., M.J.G.), University of Cambridge, Cambridge, UK
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A. Usman
aFrom the Department of Radiology (J.Y., A.U., J.H.G., M.J.G.), University of Cambridge, Cambridge, UK
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T. Das
bDepartment of Radiology (T.D., A.J.P., M.J.G.), Cambridge University Hospitals National Health Service Foundation Trust, Cambridge, UK.
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A.J. Patterson
bDepartment of Radiology (T.D., A.J.P., M.J.G.), Cambridge University Hospitals National Health Service Foundation Trust, Cambridge, UK.
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J.H. Gillard
aFrom the Department of Radiology (J.Y., A.U., J.H.G., M.J.G.), University of Cambridge, Cambridge, UK
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M.J. Graves
aFrom the Department of Radiology (J.Y., A.U., J.H.G., M.J.G.), University of Cambridge, Cambridge, UK
bDepartment of Radiology (T.D., A.J.P., M.J.G.), Cambridge University Hospitals National Health Service Foundation Trust, Cambridge, UK.
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Abstract

SUMMARY: Atherosclerosis remains the leading cause of long-term mortality and morbidity worldwide, despite remarkable advancement in its management. Vulnerable atherosclerotic plaques are principally responsible for thromboembolic events in various arterial territories such as carotid, coronary, and lower limb vessels. Carotid plaque ulceration is one of the key features associated with plaque vulnerability and is considered a notable indicator of previous plaque rupture and possible future cerebrovascular events. Multiple imaging modalities have been used to assess the degree of carotid plaque ulceration for diagnostic and research purposes. Early diagnosis and management of carotid artery disease could prevent further cerebrovascular events. In this review, we highlight the merits and limitations of various imaging techniques for identifying plaque ulceration.

ABBREVIATIONS:

CE-MRA
contrast-enhanced MRA
CDUS
color Doppler ultrasound
CEUS
contrast-enhanced ultrasound
US
ultrasound
XRA
x-ray contrast angiography

Stroke is considered the leading cause of death and long-term disability worldwide.1 Carotid atherosclerosis is one of the major causes of ischemic stroke.2 Morphologic features such as plaque ulceration are strongly correlated with ischemic stroke and coronary events, with hazard ratio ranges from 1.2 to 7.7,3⇓⇓⇓⇓–8 as summarized in Table 1. The hazard ratio is comparable with other high-risk factors such as large lipid core (hazard ratio = 1.75) and intraplaque hemorrhage (hazard ratio = 5.85).9

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Table 1:

Summary of the hazard ratios of carotid ulceration for future events risk in different studies

Carotid plaque ulceration or surface irregularity is characterized as an indentation, fissure, or erosion on the luminal surface of a plaque, exposing a portion of the inner plaque to direct contact with the circulating blood.10 Various factors are involved in the pathogenesis of ulceration, including the accumulation of inflammatory cells, proteolytic enzymes released by macrophages, and local hemodynamic factors.11 These factors weaken the fibrotic cap, leading to plaque rupture and leaving behind the ulceration. These ulcerations act as a thromboembolic source, allowing plaque components to be released into the blood. Ulcerated plaques are considered the main foci of cerebral microemboli.12

Plaque ulceration can be visualized grossly following carotid endarterectomy and later by histologic analysis of the specimen. Figure 1 shows histologic images of an ulcerated plaque.13 Early detection of plaque ulceration before an operation is essential because it may assist in preventing further thromboembolic events; therefore, there has been substantial research to evaluate different radiographic techniques in the early identification of plaque ulceration.

Fig 1.
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Fig 1.

Histologic section of an ulcerated plaque by using a hematoxylin-eosin stain showing the ulceration (left). The CD68 stain shows macrophages (middle), and the smooth-muscle actin stain shows a lack of smooth-muscle cells (right). Reprinted with permission from Gillard et al.13 Copyright Cambridge University Press 2007.

Various imaging modalities are used to assess plaque ulceration for diagnostic and research purposes (Table 2 and On-line Table). These include x-ray contrast angiography (XRA), B-mode and Doppler sonography, CTA, and MRA. The purpose of this article was to compare the different clinical imaging modalities in observing carotid ulceration from existing literature and evaluate the diagnostic value of each method.

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Table 2:

Summary of details in each imaging modality

X-Ray Contrast Angiography

X-ray contrast angiography, including conventional carotid angiography or DSA, is an established method of assessing carotid artery disease. Conventional angiography involves the acquisition of digital fluoroscopic images in combination with the administration of an iodinated contrast medium. DSA produces the angiography by subtracting the postcontrast images from precontrast images to achieve better visualization of the blood vessels. Previously, XRA was considered a criterion standard for the assessment of carotid artery disease because of its high spatial (50 μm) and temporal resolution (10 ms). It has the ability to depict the stenotic lumen and various plaque characteristics such as surface irregularities or large ulcerations. It has the advantage of visualizing a long segment of the artery at a single time point.

XRA has been widely used in large, randomized clinical trials, such as the North American Symptomatic Carotid Endarterectomy Trial (NASCET),14 the European Carotid Surgery Trial (ECST),15 and the Asymptomatic Carotid Atherosclerosis Study (ACAS).16 A study comparing angiographic surface morphology with detailed histology has concluded that ulceration detected by XRA was associated with plaque rupture, intraplaque hemorrhage, and overall plaque instability.17 An example of plaque ulceration on XRA is shown in Fig 2.

Fig 2.
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Fig 2.

DSA image of 2 large ulcerations (arrows) of a right internal carotid artery. Reprinted with permission from Gillard et al.13 Copyright Cambridge University Press 2007.

However, there are several limitations to the extensive use of XRA, especially in the carotid territory. XRA involves ionizing radiation. It is a high-cost and time-consuming procedure and requires adequate bed rest after the investigation. The invasive nature of this procedure increases the risk of creating emboli, resulting in subsequent cerebrovascular events.16,18,19 In an article based on ACAS, there was a 1.2% risk of persisting neurologic deficits or death following XRA, while the surgical risk was only 1.5%.16 Another article based on NASCET showed that a 0.7% risk of persistent neurologic deficits or death was associated with the angiography.19 XRA is not safe in patients with coagulopathies and bleeding disorders. The accuracy of XRA in detecting ulceration also depends on the degree of stenosis.20 Finally, the rates of false-positives and false-negatives of XRA were high in identifying ulcerations.21 Two possible reasons for its low accuracy in detecting ulceration are that it is operator-dependent and DSA generally acquires only a limited number of projections. These issues result in failures to detect ulceration21,22 and a tendency to underestimate stenosis.23

Based on the above-mentioned reasons, there has been a trend to replace XRA with alternative cost-effective, safe, and less time-consuming carotid imaging modalities, which are discussed below.

Sonography

Sonography was introduced as the first platform to visualize the in vivo human vessel and atherosclerosis.24 It helps to classify the plaque texture as either homogeneous (uniform consistency) or heterogeneous (nonuniform consistency).25 Homogeneous plaques present with a uniform echo intensity and show a regular, smooth surface, while heterogeneous plaques show a nonuniform pattern with mixed echo intensities and usually have an irregular/ulcerated surface.25 The plaque surface can be defined as smooth and regular, mildly irregular, or ulcerated in the case of a variation in height between 0.4 and 2 mm on the contour of the plaque.26 An example of ulceration in Doppler sonography is shown in Fig 3A. However, it is difficult to detect plaque ulceration by sonography due to various limitations. First, the overall accuracy of using B-mode sonography against criterion standard techniques (DSA or histopathology) is not high (sensitivity and specificity ranges from 39% to 89% and 72% to 87%, respectively).27⇓–29 Several studies have noted that its accuracy decreases with the increasing degree of stenosis,30,31 and it has even failed to detect ulceration in high-grade stenosis.29 The application of color-flow Doppler-assisted duplex imaging, which combines the B-mode and blood-flow velocity information,32 also shows limitations in providing adequate information to identify plaque ulcerations.31,33 Second, the intrareader reproducibility of both B-mode and Doppler sonography is low (κ ranges from 0.11 to 0.8931,34⇓–36), which is not sufficient for reliable diagnosis. Third, the criteria for carotid ulceration diagnosis are very subjective and may vary from reader to reader or center to center; this variation makes its use difficult for multicenter trials.37

Fig 3.
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Fig 3.

A, Doppler sonography shows an internal carotid artery plaque ulceration (white arrow) The asterisk shows weakly echogenic plaque material, presumably lipid. Reprinted with permission from Gillard et al.13 Copyright Cambridge University Press 2007. B, The calcification in the anterior vessel wall (white arrow) shadows the color Doppler signal and opposite wall structures (yellow arrow). JV indicates jugular vein; CCA, common carotid artery. Adapted from Steinke et al.39

These limitations are mostly due to the native imaging principle. 2D sonography can only obtain a 2D cut plane of the carotid area; this could introduce operator error when the sonography probe is not parallel to the vessel axis or the orientation of the ulceration.38 Also, the presence of calcification reflects the acoustic wave, which can obscure ulceration.38 An example of artifacts due to calcification is shown in Fig 3B.39

The use of microbubble contrast agents has been shown to improve accuracy. A direct comparison of contrast-enhanced ultrasound (CEUS) and color Doppler ultrasound (CDUS) observed that CEUS has superior sensitivity and diagnostic accuracy over CDUS in detecting ulceration.40 Within the same study, CEUS detected more ulceration than CTA, especially small ulcerations, attributed to the higher spatial and temporal resolution achieved in CEUS.40 Further CEUS studies will be required to verify the improved accuracy of this technique. The safety of using CEUS should also be considered, including toxicity, microembolism, and inertial cavitation caused by the microbubbles.41

The recent development of 3D sonography has demonstrated superior ability in detecting ulceration compared with conventional 2D sonography (Fig 4).36,42 3D sonographic images can be obtained by using dedicated 3D probes or by using 2D sonographic probes with the help of positioning sensors and postreconstruction algorithms to combine 2D sections into a 3D volume.43,44 This process improves image quality, provides more information about plaque morphology and echomorphology, and has been used to noninvasively quantify plaque stenosis45 and volume46,47 and examine the regression and progression of plaque ulceration.42 By comparing 3D and 2D sonography in 142 patients, Heliopoulos et al36 showed that 3D methods depicted more ulcerations than the 2D methods (15% versus 8% of plaques) and also had higher interobserver reproducibility (κ = 0.973, standard error = 0.027, versus κ = 0.885, standard error = 0.055). However, this methodology is still under development and requires further validation against accepted criterion standard techniques such as DSA and histopathology.

Fig 4.
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Fig 4.

A, 2D sonography depicts a smooth plaque, arrow shows the stenosis. B, 3D sonography shows an ulceration of the same plaque in another plane, arrow shows an ulcer at site of shear stress. The figure is adapted with permission from Heliopoulos et al.36

CTA

Studies with CTA have demonstrated that plaque ulceration is closely associated with increased lipid volume,48,49 an increased degree of stenosis,38 plaque volume, and decreased calcification proportions.49 Surgical observations have shown good correlation, with CTA having a high sensitivity (94%) and specificity (99%) to detect plaque ulceration.50 Compared with sonography, CTA showed higher sensitivity and specificity to detect ulceration.38

In comparison with DSA, CTA has fewer associated complications,38 while its accuracy in the determination of ulceration still needs more research for validation. One major limitation of CTA in detecting ulceration is the appearance of plaque calcification.51

The recent development of dual-source CT, which uses 2 x-ray energies simultaneously to separate high-density calcification and the contrast-enhanced lumen, has shown advantages for evaluating densely calcified carotid stenosis and could be more accurate.52,53 Figure 5 shows that the morphology of ulcerations cannot be visualized clearly by conventional CTA due to calcification, while dual-source CTA software could remove the calcification from the image, making the ulcer clearer.

Fig 5.
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Fig 5.

A, An ulceration (yellow arrow) in a heavily calcified (white arrows) plaque. B, The ulcer is clearer with the calcification removed by dual-energy CTA.

Like XRA, a drawback of CTA is the use of ionizing radiation. In imaging the neck vessels, the radiation dose of CTA is equivalent to or higher compared with that in DSA.54,55 Also, the use of contrast media may be contraindicated in some patients with poor renal function.56

MR Imaging

Noncontrast-Enhanced MRA.

The most common method for MRA is time-of-flight, which relies on the high MR imaging signal from the moving blood within the vessel lumen to create vascular contrast.57 Both 2D (ie, multi-slice58) and 3D (ie, volumetric57,59) TOF have been used for carotid artery imaging. One of the biggest advantages of MRA over DSA and US is that the images can be reformatted into any orientation after the acquisition.

However, one of the well-known limitations of TOF-MRA is that signal saturation and dephasing of the signal could lead to a signal loss from focal areas of complex flow.60 The stenosis measurement accuracy of TOF is dependent on the wash-in efficiency of unsaturated spins within the imaging section/slab. For large ulcerations, the hemodynamic patterns of blood flow are complicated.61 Ulceration detection could therefore be limited if the saturated spins are not replaced by fresh unsaturated blood flow. Also, the orientation of the imaging section/slab is important. TOF techniques are limited to the flow orthogonal or at a certain angle to the imaging sections/slabs. The signal from flowing blood parallel to the imaging sections/slabs can become saturated.59 In addition, the ulceration orientation, location, and shape could also influence the accuracy of measurements with TOF-MRA.61 Spatial resolution would be another limitation of TOF-MRA, especially for very small ulcers.59 In addition, patient motion during relatively long acquisition times is another limitation.59

In recent years, other non-contrast-enhanced MRA techniques have emerged claiming to overcome some of the limitations of TOF-MRA. Arterial spin-labeling–based methods subtract images where fresh flowing blood has been magnetically “labeled” from images without labeling. Such methods have demonstrated the ability to image arteries of the head and neck without signal from static background.62,63 In particular, a hybrid of pseudocontinuous and pulsed arterial spin-labeling with a fast low-angle shot readout has shown similar results in detecting carotid luminal irregularity with contrast-enhanced MRA (CE-MRA) and overcomes some of the limitations of TOF-MRA (Fig 6).63 The inversion recovery–based methods64 and the quiescent interval low-angle shot method65 use in-plane saturation pulses to suppress the background signal, allowing only the nonsaturated inflowing blood to be imaged. Blood-suppression–based methods use the subtraction of images with and without blood-suppression preparation pulses and have also shown good images of arteries and veins.66 Because these methods have only recently been developed, more studies are necessary to validate their accuracy in detecting plaque ulceration.

Fig 6.
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Fig 6.

Luminal irregularity in the internal carotid artery is demonstrated on both a nonenhanced hybrid of pseudocontinuous and pulsed arterial spin-labeling (arrow, A) and CE-MRA (C) images, but it is not seen on the 3D TOF image (dashed arrow, B). hASL indicates hybrid of pseudocontinuous and pulsed ASL. The figure is reproduced with permission from Koktzoglou et al.63

Contrast-Enhanced MRA.

CE-MRA is an MR imaging technique for vascular imaging that exploits the use of an intravenously administered paramagnetic contrast agent (ie, a chelate of gadolinium) to shorten the T1 relaxation time of the blood, providing excellent contrast with the background tissues. Because the images are no longer dependent on the inflow of the blood, CE-MRA produces high-quality images in a short timeframe and may reduce some of the drawbacks associated with TOF-MRA. In 1 study, the prevalence of plaque ulceration was 86% in a symptomatic patient cohort compared with 36% in an asymptomatic patient group, indicating that CE-MRA could be used for detecting ulceration.67 CE-MRA has also been shown to detect more ulcers than TOF-MRA.61 Figure 7A shows an internal carotid artery with several ulcerations demonstrated by CE-MRA; however, all were missed by TOF-MRA (Fig 7B). In addition, CE-MRA has the advantage of depicting ulceration in calcified plaques, which is one of the limitations of standard CTA (Fig 7C). The images were processed by using a dedicated workstation (Advantage Windows 4.6; GE Healthcare, Milwaukee, Wisconsin).

Fig 7.
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Fig 7.

High-resolution MR imaging, CTA, and sonography of the left carotid artery of a 77-year-old man. Ulcerations (yellow arrow) are shown clearly on CE-MRA (A) and pre- and postcontrast black-blood T1-weighted (D and E) images; however, they were missed on TOF-MRA (B). The calcification on CTA (white arrow, C) causes difficulty when observing the ulceration. Doppler sonography (F) shows no ulceration in the internal carotid artery.

Although CE-MRA shows high accuracy in detecting plaque ulceration, it is still a relatively expensive examination. MR imaging is not suitable for patients with contraindications such as implanted devices. In addition, the use of gadolinium-based contrast agents may be contraindicated in patients with severe renal impairment (eg, glomerular filtration rate < 30), which may limit its wider application.

Blood-Suppressed MR Morphologic Imaging.

High-resolution standard MR images are widely used for carotid morphologic imaging; however, the signal from flowing blood in the lumen makes it difficult to identify the vessel wall. Blood suppression is usually achieved through a signal-preparation scheme applied before the imaging sequence. The most commonly used schemes include double or quadruple inversion recovery,68,69 motion-sensitive driven equilibrium,70 and delay alternating with nutation for tailored excitation (DANTE).71 Multicontrast cross-sectional MR imaging with blood could also be used for ulceration detection.72,73 Figure 7D, -E shows an example of carotid ulceration in DANTE-prepared pre- and postcontrast T1-weighted images.

Discussion

Carotid ulceration is now considered a major hallmark in determining the vulnerability of atherosclerotic plaque because it indicates a previous plaque rupture and is a strong predictor of subsequent events. The identification of plaque ulceration may assist in the appropriate management of patients at risk of future ischemic events. We have reviewed the literature regarding the various radiologic techniques used to demonstrate plaque ulceration.

A direct comparison of the sensitivity and specificity of different imaging modalities is difficult because the definition of plaque ulceration varies in different studies. Pathologically, ulceration is defined as an erosion of the single cell–layer intima by microscopic examination74⇓–76 or surface defects more than a certain value (such as 560 μm or 1 mm in diameter and depth) in gross photography.12,28,29,77 In some studies with DSA,17 CTA,49,78 and MRA,67,79 a general definition “the extended lumen into plaque” has been used. In some of the CTA studies, a more specific definition has been described, such as the intimal defect must be larger than 1 mm in width38,48,50 or 2 mm in depth.80

Sonography is limited by its accuracy and reproducibility, especially when the lesion is calcified. The recent development of 3D US and the use of CEUS may help improve the detection of carotid ulceration.

CTA is relatively safe compared with XRA and much faster and cheaper than MR imaging. However, as with XRA, ionization must be considered when using CTA. Optimization of the scanning protocol and the use of new reconstruction techniques81 can help reduce the radiation dose. The application of dual-source CTA may also help to improve the sensitivity and accuracy in detecting ulceration within calcified plaques.

The advantage of MR imaging is that morphologic and functional features of carotid plaque can be obtained within a single examination. These features could help provide a comprehensive assessment of plaque vulnerability. Non-contrast-enhanced MRA techniques have shown comparable efficiency with CE-MRA for detecting ulceration and could be used in patients with contraindications to contrast agents. By improving the resolution and optimizing the acquisition sequence, non-contrast-enhanced MRA techniques may identify smaller ulcerations missed by current MR imaging methods.

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REFERENCES

  1. 1.↵
    World Health Organization. Cardiovascular Diseases (CVDs): Fact Sheet No. 317. 2011. Geneva: World Health Organization Google Scholar; 2011
  2. 2.↵
    1. Kistler JP,
    2. Furie KL
    . Carotid endarterectomy revisited. N Engl J Med 2000;342:1743–45 doi:10.1056/NEJM200006083422310 pmid:10841879
    CrossRefPubMed
  3. 3.↵
    1. Eliasziw M,
    2. Streifler JY,
    3. Fox AJ, et al
    . Significance of plaque ulceration in symptomatic patients with high-grade carotid stenosis: North American Symptomatic Carotid Endarterectomy Trial. Stroke 1994;25:304–08 doi:10.1161/01.STR.25.2.304 pmid:8303736
    Abstract/FREE Full Text
  4. 4.↵
    1. Handa N,
    2. Matsumoto M,
    3. Maeda H, et al
    . Ischemic stroke events and carotid atherosclerosis: results of the Osaka follow-up study for ultrasonographic assessment of carotid atherosclerosis (the OSACA Study). Stroke 1995;26:1781–86 doi:10.1161/01.STR.26.10.1781 pmid:7570725
    Abstract/FREE Full Text
  5. 5.↵
    1. Rothwell P,
    2. Villagra R,
    3. Gibson R, et al
    . Evidence of a chronic systemic cause of instability of atherosclerotic plaques. Lancet 2000;355:19–24 doi:10.1016/S0140-6736(99)04470-0 pmid:10615886
    CrossRefPubMed
  6. 6.↵
    1. Rothwell PM,
    2. Gibson R,
    3. Warlow C
    . Interrelation between plaque surface morphology and degree of stenosis on carotid angiograms and the risk of ischemic stroke in patients with symptomatic carotid stenosis: on behalf of the European Carotid Surgery Trialists' Collaborative Group. Stroke 2000;31:615–21 doi:10.1161/01.STR.31.3.615 pmid:10700494
    Abstract/FREE Full Text
  7. 7.↵
    1. Prabhakaran S,
    2. Rundek T,
    3. Ramas R, et al
    . Carotid plaque surface irregularity predicts ischemic stroke: the northern Manhattan study. Stroke 2006;37:2696–701 doi:10.1161/01.STR.0000244780.82190.a4 pmid:17008627
    Abstract/FREE Full Text
  8. 8.↵
    1. Rothwell PM,
    2. Mehta Z,
    3. Howard SC, et al
    . Treating individuals 3: from subgroups to individuals—general principles and the example of carotid endarterectomy. Lancet 2005;365:256–65 doi:10.1016/S0140-6736(05)70156-2 pmid:15652609
    CrossRefPubMed
  9. 9.↵
    1. Sadat U,
    2. Teng Z,
    3. Young V, et al
    . Association between biomechanical structural stresses of atherosclerotic carotid plaques and subsequent ischaemic cerebrovascular events–a longitudinal in vivo magnetic resonance imaging-based finite element study. Eur J Vasc Endovasc Surg 2010;40:485–91 doi:10.1016/j.ejvs.2010.07.015 pmid:20724181
    CrossRefPubMed
  10. 10.↵
    1. Miskolczi L,
    2. Guterman LR,
    3. Flaherty JD, et al
    . Depiction of carotid plaque ulceration and other plaque-related disorders by intravascular sonography: a flow chamber study. AJNR Am J Neuroradiol 1996;17:1881–90 pmid:8933872
    Abstract
  11. 11.↵
    1. Stary HC,
    2. Chandler AB,
    3. Dinsmore RE, et al
    . A definition of advanced types of atherosclerotic lesions and a histological classification of atherosclerosis: a report from the Committee on Vascular Lesions of the Council on Arteriosclerosis, American Heart Association. Circulation 1995;92:1355–74 doi:10.1161/01.CIR.92.5.1355 pmid:7648691
    Abstract/FREE Full Text
  12. 12.↵
    1. Sitzer M,
    2. Müller W,
    3. Siebler M, et al
    . Plaque ulceration and lumen thrombus are the main sources of cerebral microemboli in high-grade internal carotid artery stenosis. Stroke 1995;26:1231–33 doi:10.1161/01.STR.26.7.1231 pmid:7604420
    Abstract/FREE Full Text
  13. 13.↵
    1. Gillard J,
    2. Graves M,
    3. Hatsukami T, et al
    . Carotid Disease: The Role of Imaging in Diagnosis and Management. Cambridge: Cambridge University Press; 2007:133
  14. 14.↵
    North American Symptomatic Carotid Endarterectomy Trial Collaborators. Beneficial effect of carotid endarterectomy in symptomatic patients with high-grade carotid stenosis. N Engl J Med 1991;325:445–53 doi:10.1056/NEJM199108153250701 pmid:1852179
    CrossRefPubMed
  15. 15.↵
    Randomised trial of endarterectomy for recently symptomatic carotid stenosis: final results of the MRC European Carotid Surgery Trial (ECST). Lancet 1998;351:1379–87 doi:10.1016/S0140-6736(97)09292-1 pmid:9593407
    CrossRefPubMed
  16. 16.↵
    Endarterectomy for asymptomatic carotid artery stenosis: Executive Committee for the Asymptomatic Carotid Atherosclerosis Study. JAMA 1995;273:1421–28 pmid:7723155
    CrossRefPubMed
  17. 17.↵
    1. Lovett J,
    2. Gallagher P,
    3. Hands L, et al
    . Histological correlates of carotid plaque surface morphology on lumen contrast imaging. Circulation 2004;110:2190–97 doi:10.1161/01.CIR.0000144307.82502.32 pmid:15466633
    Abstract/FREE Full Text
  18. 18.↵
    1. Hessel SJ,
    2. Adams DF,
    3. Abrams HL
    . Complications of angiography. Radiology 1981;138:273–81 doi:10.1148/radiology.138.2.7455105 pmid:7455105
    CrossRefPubMed
  19. 19.↵
    1. Barnett HJ,
    2. Meldrum HE,
    3. Eliasziw M
    ; North American Symptomatic Carotid Endarterectomy Trial (NASCET) collaborators. The appropriate use of carotid endarterectomy. CMAJ 2002;166:1169–79 pmid:12000252
    Abstract/FREE Full Text
  20. 20.↵
    1. Edwards JH,
    2. Kricheff II,
    3. Riles T, et al
    . Angiographically undetected ulceration of the carotid bifurcation as a cause of embolic stroke. Radiology 1979;132:369–73 doi:10.1148/132.2.369 pmid:461794
    CrossRefPubMed
  21. 21.↵
    1. Streifler JY,
    2. Eliasziw M,
    3. Fox AJ, et al
    . Angiographic detection of carotid plaque ulceration: comparison with surgical observations in a multicenter study—North American Symptomatic Carotid Endarterectomy Trial. Stroke 1994;25:1130–32 doi:10.1161/01.STR.25.6.1130 pmid:8202969
    Abstract/FREE Full Text
  22. 22.↵
    1. Gandhi D
    . Computed tomography and magnetic resonance angiography in cervicocranial vascular disease. J Neuroophthalmol 2004;24:306–14 doi:10.1097/00041327-200412000-00008 pmid:15662247
    CrossRefPubMed
  23. 23.↵
    1. Ho VB,
    2. Foo TK
    . Optimization of gadolinium-enhanced magnetic resonance angiography using an automated bolus-detection algorithm (MR SmartPrep): original investigation. Invest Radiol 1998;33:515–23 doi:10.1097/00004424-199809000-00006 pmid:9766035
    CrossRefPubMed
  24. 24.↵
    1. Barnes R,
    2. Bone G,
    3. Reinertson J, et al
    . Noninvasive ultrasonic carotid angiography: prospective validation by contrast arteriography. Surgery 1976;80:328–35 pmid:960001
    PubMed
  25. 25.↵
    1. Reilly LM,
    2. Lusby RJ,
    3. Hughes L, et al
    . Carotid plaque histology using real-time ultrasonography: clinical and therapeutic implications. Am J Surg 1983;146:188–93 doi:10.1016/0002-9610(83)90370-7 pmid:6192733
    CrossRefPubMed
  26. 26.↵
    1. Dósa E,
    2. Hirschberg K,
    3. Apor A, et al
    . Echolucent or predominantly echolucent femoral plaques predict early restenosis after eversion carotid endarterectomy. J Vasc Surg 2010;51:345–50 doi:10.1016/j.jvs.2009.08.080 pmid:20141957
    CrossRefPubMed
  27. 27.↵
    1. O'Donnell TF,
    2. Erdoes L,
    3. Mackey WC, et al
    . Correlation of B-mode ultrasound imaging and arteriography with pathologic findings at carotid endarterectomy. Arch Surg 1985;120:443–49 doi:10.1001/archsurg.1985.01390280037009 pmid:3885910
    CrossRefPubMed
  28. 28.↵
    1. O'Leary D,
    2. Holen J,
    3. Ricotta J, et al
    . Carotid bifurcation disease: prediction of ulceration with B-mode US. Radiology 1987;162:523–25 doi:10.1148/radiology.162.2.3541034 pmid:3541034
    CrossRefPubMed
  29. 29.↵
    1. Comerota AJ,
    2. Katz ML,
    3. White JV, et al
    . The preoperative diagnosis of the ulcerated carotid atheroma. J Vasc Surg 1990;11:505–10 pmid:2182913
    CrossRefPubMed
  30. 30.↵
    1. Hennerici M,
    2. Baezner H,
    3. Daffertshofer M
    . Ultrasound and arterial wall disease. Cerebrovasc Dis 2004;17:19–33 pmid:14694277
    CrossRefPubMed
  31. 31.↵
    1. Sitzer M,
    2. Müller W,
    3. Rademacher J, et al
    . Color-flow Doppler-assisted duplex imaging fails to detect ulceration in high-grade internal carotid artery stenosis. J Vasc Surg 1996;23:461–65 doi:10.1016/S0741-5214(96)80011-5 pmid:8601888
    CrossRefPubMed
  32. 32.↵
    1. Mitchell DG
    . Color Doppler imaging: principles, limitations, and artifacts. Radiology 1990;177:1–10 doi:10.1148/radiology.177.1.2204956 pmid:2204956
    CrossRefPubMed
  33. 33.↵
    1. De Bray J,
    2. Baud J,
    3. Dauzat M
    . Consensus concerning the morphology and the risk of carotid plaques. Cerebrovasc Dis 1997;7:289–96 doi:10.1159/000108415
    CrossRef
  34. 34.↵
    1. Anderson DC,
    2. Loewenson R,
    3. Yock D, et al
    . B-mode, real-time carotid ultrasonic imaging: correlation with angiography. Arch Neurol 1983;40:484–88 doi:10.1001/archneur.1983.04210070024008 pmid:6870608
    CrossRefPubMed
  35. 35.↵
    1. O'Leary D,
    2. Bryan F,
    3. Goodison M, et al
    . Measurement variability of carotid atherosclerosis: real-time (B-mode) ultrasonography and angiography. Stroke 1987;18:1011–17 doi:10.1161/01.STR.18.6.1011 pmid:3317999
    Abstract/FREE Full Text
  36. 36.↵
    1. Heliopoulos J,
    2. Vadikolias K,
    3. Piperidou C, et al
    . Detection of carotid artery plaque ulceration using 3-dimensional ultrasound. J Neuroimaging 2011;21:126–31 doi:10.1111/j.1552-6569.2009.00450.x pmid:19888925
    CrossRefPubMed
  37. 37.↵
    1. Geroulakos G,
    2. Hobson R,
    3. Nicolaides A
    . Ultrasonographic carotid plaque morphology in predicting stroke risk. Br J Surg 1996;83:582–87 doi:10.1002/bjs.1800830505 pmid:8689198
    CrossRefPubMed
  38. 38.↵
    1. Saba L,
    2. Caddeo G,
    3. Sanfilippo R, et al
    . CT and ultrasound in the study of ulcerated carotid plaque compared with surgical results: potentialities and advantages of multidetector row CT angiography. AJNR Am J Neuroradiol 2007;28:1061–66 doi:10.3174/ajnr.A0486 pmid:17569958
    Abstract/FREE Full Text
  39. 39.↵
    1. Steinke W,
    2. Kloetzsch C,
    3. Hennerici M
    . Carotid artery disease assessed by color Doppler flow imaging: correlation with standard Doppler sonography and angiography. AJNR Am J Neuroradiol 1990;11:259–66 pmid:2107709
    Abstract/FREE Full Text
  40. 40.↵
    1. ten Kate GL,
    2. van Dijk AC,
    3. van den Oord SC, et al
    . Usefulness of contrast-enhanced ultrasound for detection of carotid plaque ulceration in patients with symptomatic carotid atherosclerosis. Am J Cardiol 2013;112:292–98 doi:10.1016/j.amjcard.2013.03.028 pmid:23587280
    CrossRefPubMed
  41. 41.↵
    1. Stride E,
    2. Saffari N
    . Microbubble ultrasound contrast agents: a review. Proc Inst Mech Eng H 2003;217:429–47 doi:10.1243/09544110360729072 pmid:14702981
    CrossRefPubMed
  42. 42.↵
    1. Schminke U,
    2. Motsch L,
    3. Hilker L, et al
    . Three-dimensional ultrasound observation of carotid artery plaque ulceration. Stroke 2000;31:1651–55 doi:10.1161/01.STR.31.7.1651 pmid:10884468
    Abstract/FREE Full Text
  43. 43.↵
    1. Fenster A,
    2. Downey DB,
    3. Cardinal HN
    . Three-dimensional ultrasound imaging. Phys Med Boil 2001;46:R67 doi:10.1088/0031-9155/46/5/201 pmid:138407
    CrossRefPubMed
  44. 44.↵
    1. Solberg OV,
    2. Lindseth F,
    3. Torp H, et al
    . Freehand 3D ultrasound reconstruction algorithms: a review. Ultrasound Med Boil 2007;33:991–1009 doi:10.1016/j.ultrasmedbio.2007.02.015 pmid:17512655
    CrossRefPubMed
  45. 45.↵
    1. Yao J,
    2. van Sambeek MR,
    3. Dall'Agata A, et al
    . Three-dimensional ultrasound study of carotid arteries before and after endarterectomy: analysis of stenotic lesions and surgical impact on the vessel. Stroke 1998;29:2026–31 doi:10.1161/01.STR.29.10.2026 pmid:9756576
    Abstract/FREE Full Text
  46. 46.↵
    1. Griewing B,
    2. Schminke U,
    3. Morgenstern C, et al
    . Three-dimensional ultrasound angiography (power mode) for the quantification of carotid artery atherosclerosis. J Neuroimaging 1997;7:40–45 doi:10.1111/jon19977140 pmid:9038431
    CrossRefPubMed
  47. 47.↵
    1. Palombo C,
    2. Kozakova M,
    3. Morizzo C, et al
    . Ultrafast three-dimensional ultrasound application to carotid artery imaging. Stroke 1998;29:1631–37 doi:10.1161/01.STR.29.8.1631 pmid:9707205
    Abstract/FREE Full Text
  48. 48.↵
    1. Saba L,
    2. Sanfilippo R,
    3. Sannia S, et al
    . Association between carotid artery plaque volume, composition, and ulceration: a retrospective assessment with MDCT. AJR Am J Roentgenol 2012;199:151–56 doi:10.2214/AJR.11.6955 pmid:22733906
    CrossRefPubMed
  49. 49.↵
    1. Homburg PJ,
    2. Rozie S,
    3. van Gils MJ, et al
    . Association between carotid artery plaque ulceration and plaque composition evaluated with multidetector CT angiography. Stroke 2011;42:367–72 doi:10.1161/STROKEAHA.110.597369 pmid:21183745
    Abstract/FREE Full Text
  50. 50.↵
    1. Saba L,
    2. Caddeo G,
    3. Sanfilippo R, et al
    . Efficacy and sensitivity of axial scans and different reconstruction methods in the study of the ulcerated carotid plaque using multidetector-row CT angiography: comparison with surgical results. AJNR Am J Neuroradiol 2007;28:716–23 pmid:17416828
    Abstract/FREE Full Text
  51. 51.↵
    1. Link J,
    2. Brossmann J,
    3. Grabener M, et al
    . Spiral CT angiography and selective digital subtraction angiography of internal carotid artery stenosis. AJNR Am J Neuroradiol 1996;17:89–94 pmid:8770255
    Abstract
  52. 52.↵
    1. Korn A,
    2. Bender B,
    3. Thomas C, et al
    . Dual energy CTA of the carotid bifurcation: advantage of plaque subtraction for assessment of grade of the stenosis and morphology. Eur J Radiol 2011;80:e120–25 doi:10.1016/j.ejrad.2010.08.028 pmid:20833492
    CrossRefPubMed
  53. 53.↵
    1. Vlahos I,
    2. Chung R,
    3. Nair A, et al
    . Dual-energy CT: vascular applications. AJR Am J Roentgenol 2012;199:S87–97 doi:10.2214/AJR.12.9114 pmid:23097172
    CrossRefPubMed
  54. 54.↵
    1. Klingebiel R,
    2. Kentenich M,
    3. Bauknecht H-C, et al
    . Comparative evaluation of 64-slice CT angiography and digital subtraction angiography in assessing the cervicocranial vasculature. Vasc Health Risk Manag 2008;4:901–07 pmid:19066008
    PubMed
  55. 55.↵
    1. Manninen AL,
    2. Isokangas JM,
    3. Karttunen A, et al
    . A comparison of radiation exposure between diagnostic CTA and DSA examinations of cerebral and cervicocerebral vessels. AJNR Am J Neuroradiol 2012;33:2038–42 doi:10.3174/ajnr.A3123 pmid:22700752
    Abstract/FREE Full Text
  56. 56.↵
    1. Hasebroock KM,
    2. Serkova NJ
    . Toxicity of MRI and CT contrast agents. Expert Opin Drug Metab Toxicol 2009;5:403–16 doi:10.1517/17425250902873796 pmid:19368492
    CrossRefPubMed
  57. 57.↵
    1. Laub GA,
    2. Kaiser WA
    . MR angiography with gradient motion refocusing. J Comput Assist Tomogr 1988;12:377–82 doi:10.1097/00004728-198805010-00002 pmid:3366945
    CrossRefPubMed
  58. 58.↵
    1. Gullberg GT,
    2. Wehrli FW,
    3. Shimakawa A, et al
    . MR vascular imaging with a fast gradient refocusing pulse sequence and reformatted images from transaxial sections. Radiology 1987;165:241–46 doi:10.1148/radiology.165.1.3628776 pmid:3628776
    CrossRefPubMed
  59. 59.↵
    1. Anderson C,
    2. Saloner D,
    3. Lee R, et al
    . Assessment of carotid artery stenosis by MR angiography: comparison with x-ray angiography and color-coded Doppler ultrasound. AJNR Am J Neuroradiol 1992;13:989–1003; discussion 1005–08 pmid:1590203
    Abstract/FREE Full Text
  60. 60.↵
    1. Yucel EK,
    2. Anderson CM,
    3. Edelman RR, et al
    . AHA scientific statement: magnetic resonance angiography update on applications for extracranial arteries. Circulation 1999;100:2284–301 doi:10.1161/01.CIR.100.22.2284 pmid:10578005
    FREE Full Text
  61. 61.↵
    1. Etesami M,
    2. Hoi Y,
    3. Steinman D, et al
    . Comparison of carotid plaque ulcer detection using contrast-enhanced and time-of-flight MRA techniques. AJNR Am J Neuroradiol 2013;34:177–84 doi:10.3174/ajnr.A3132 pmid:22627797
    Abstract/FREE Full Text
  62. 62.↵
    1. Raoult H,
    2. Gauvrit JY,
    3. Schmitt P, et al
    . Non-ECG-gated unenhanced MRA of the carotids: optimization and clinical feasibility. Eur Radiol 2013;23:3020–28 doi:10.1007/s00330-013-2931-x pmid:23783783
    CrossRefPubMed
  63. 63.↵
    1. Koktzoglou I,
    2. Walker MT,
    3. Meyer JR, et al
    . Nonenhanced hybridized arterial spin labeled magnetic resonance angiography of the extracranial carotid arteries using a fast low angle shot readout at 3 Tesla. J Cardiovasc Magn Reson 2016;18:18 doi:10.1186/s12968-016-0238-1 pmid:27067840
    CrossRefPubMed
  64. 64.↵
    1. Takei N,
    2. Miyoshi M,
    3. Kabasawa H
    . Noncontrast MR angiography for supraaortic arteries using inflow enhanced inversion recovery fast spin echo imaging. J Magn Reson Imaging 2012;35:957–62 doi:10.1002/jmri.23515 pmid:22127993
    CrossRefPubMed
  65. 65.↵
    1. Koktzoglou I,
    2. Murphy IG,
    3. Giri S, et al
    . Quiescent interval low angle shot magnetic resonance angiography of the extracranial carotid arteries. Magn Reson Med 2016;75:2072–77 doi:10.1002/mrm.25791 pmid:26072706
    CrossRefPubMed
  66. 66.↵
    1. Priest AN,
    2. Graves MJ,
    3. Lomas DJ
    . Non-contrast-enhanced vascular magnetic resonance imaging using flow-dependent preparation with subtraction. Magn Reson Med 2012;67:628–37 doi:10.1002/mrm.23040 pmid:21713977
    CrossRefPubMed
  67. 67.↵
    1. Demarco J,
    2. Ota H,
    3. Underhill H, et al
    . MR carotid plaque imaging and contrast-enhanced MR angiography identifies lesions associated with recent ipsilateral thromboembolic symptoms: an in vivo study at 3T. AJNR Am J Neuroradiol 2010;31:1395–402 doi:10.3174/ajnr.A2213 pmid:20651015
    Abstract/FREE Full Text
  68. 68.↵
    1. Edelman RR,
    2. Chien D,
    3. Kim D
    . Fast selective black blood MR imaging. Radiology 1991;181:655–60 doi:10.1148/radiology.181.3.1947077 pmid:1947077
    CrossRefPubMed
  69. 69.↵
    1. Yarnykh VL,
    2. Yuan C
    . T1-insensitive flow suppression using quadruple inversion-recovery. Magn Reson Med 2002;48:899–905 doi:10.1002/mrm.10292 pmid:12418006
    CrossRefPubMed
  70. 70.↵
    1. Wang J,
    2. Yarnykh VL,
    3. Hatsukami T, et al
    . Improved suppression of plaque-mimicking artifacts in black-blood carotid atherosclerosis imaging using a multislice motion-sensitized driven-equilibrium (MSDE) turbo spin-echo (TSE) sequence. Magn Reson Med 2007;58:973–81 doi:10.1002/mrm.21385 pmid:17969103
    CrossRefPubMed
  71. 71.↵
    1. Li L,
    2. Miller KL,
    3. Jezzard P
    . DANTE-prepared pulse trains: a novel approach to motion-sensitized and motion-suppressed quantitative magnetic resonance imaging. Magn Reson Med 2012;68:1423–38 doi:10.1002/mrm.24142 pmid:22246917
    CrossRefPubMed
  72. 72.↵
    1. Chu B,
    2. Yuan C,
    3. Takaya N, et al
    . Images in cardiovascular medicine: serial high-spatial-resolution, multisequence magnetic resonance imaging studies identify fibrous cap rupture and penetrating ulcer into carotid atherosclerotic plaque. Circulation 2006;113:e660–61 doi:10.1161/CIRCULATIONAHA.105.567255 pmid:16567574
    FREE Full Text
  73. 73.↵
    1. Chu B,
    2. Ferguson MS,
    3. Underhill H, et al
    . Images in cardiovascular medicine: detection of carotid atherosclerotic plaque ulceration, calcification, and thrombosis by multicontrast weighted magnetic resonance imaging. Circulation 2005;112:e3–4 doi:10.1161/CIRCULATIONAHA.104.494419 pmid:15998688
    FREE Full Text
  74. 74.↵
    1. Ackerman RH,
    2. Candia MR
    . Assessment of carotid artery stenosis by MR angiography. AJNR Am J Neuroradiol 1992;13:1005–08
    FREE Full Text
  75. 75.↵
    1. Smith RR,
    2. Russell WF,
    3. Percy ML
    . Ultrastructure of carotid plaques. Surg Neurol 1980;14:145–53 pmid:7414501
    PubMed
  76. 76.↵
    1. Hertzer NR,
    2. Beven EG,
    3. Benjamin SP
    . Ultramicroscopic ulcerations and thrombi of the carotid bifurcation. Arch Surg 1977;112:1394–1402 doi:10.1001/archsurg.1977.01370110128015 pmid:921536
    CrossRefPubMed
  77. 77.↵
    1. Fisher M,
    2. Martin A,
    3. Cosgrove M, et al
    . The NASCET-ACAS plaque project: North American Symptomatic Carotid Endarterectomy Trial—Asymptomatic Carotid Atherosclerosis Study. Stroke 1993;24:I24–25; discussion I31–32 pmid:8249015
    PubMed
  78. 78.↵
    1. Berg M,
    2. Zhang Z,
    3. Ikonen A, et al
    . Multi-detector row CT angiography in the assessment of carotid artery disease in symptomatic patients: comparison with rotational angiography and digital subtraction angiography. AJNR Am J Neuroradiol 2005;26:1022–34 pmid:15891155
    Abstract/FREE Full Text
  79. 79.↵
    1. Saouaf R,
    2. Grassi C,
    3. Hartnell G, et al
    . Complete MR angiography and Doppler ultrasound as the sole imaging modalities prior to carotid endarterectomy. Clin Radiol 1998;53:579–86 doi:10.1016/S0009-9260(98)80149-9 pmid:9744583
    CrossRefPubMed
  80. 80.↵
    1. Wintermark M,
    2. Jawadi SS,
    3. Rapp JH, et al
    . High-resolution CT imaging of carotid artery atherosclerotic plaques. AJNR Am J Neuroradiol 2008;29:875–82 doi:10.3174/ajnr.A0950 pmid:18272562
    Abstract/FREE Full Text
  81. 81.↵
    1. Silva AC,
    2. Lawder HJ,
    3. Hara A, et al
    . Innovations in CT dose reduction strategy: application of the adaptive statistical iterative reconstruction algorithm. AJR Am J Roentgenol 2010;194:191–99 doi:10.2214/AJR.09.2953 pmid:20028923
    CrossRefPubMed
  82. 82.
    1. Yao JS,
    2. Francfort J,
    3. Flinn WR, et al
    . Sonic characterization of carotid artery plaque and its surgical significance. In: Arterial Surgery: New Diagnostic and Operative Techniques. Orlando: Grune & Stratton; 1988:161–70
  83. 83.
    1. Cumming MJ,
    2. Morrow IM
    . Carotid artery stenosis: a prospective comparison of CT angiography and conventional angiography. AJR Am J Roentgenol 1994;163:517–23 doi:10.2214/ajr.163.3.8079836 pmid:8079836
    CrossRefPubMed
  84. 84.
    1. Patel MR,
    2. Kuntz KM,
    3. Klufas RA, et al
    . Preoperative assessment of the carotid bifurcation: can magnetic resonance angiography and duplex ultrasonography replace contrast arteriography? Stroke 1995;26:1753–58 doi:10.1161/01.STR.26.10.1753 pmid:7570720
    Abstract/FREE Full Text
  85. 85.
    1. Kagawa R,
    2. Moritake K,
    3. Shima T, et al
    . Validity of B-mode ultrasonographic findings in patients undergoing carotid endarterectomy in comparison with angiographic and clinicopathologic features. Stroke 1996;27:700–05 doi:10.1161/01.STR.27.4.700 pmid:8614934
    Abstract/FREE Full Text
  86. 86.
    1. Randoux B,
    2. Marro B,
    3. Koskas F, et al
    . Carotid artery stenosis: prospective comparison of CT, three-dimensional gadolinium-enhanced MR, and conventional angiography. Radiology 2001;220:179–85 doi:10.1148/radiology.220.1.r01jl35179 pmid:11425993
    CrossRefPubMed
  87. 87.
    1. Berg M,
    2. Manninen H,
    3. Räsänen H, et al
    . CT angiography in the assessment of carotid artery atherosclerosis. Acta Radiol 2002;43:116–24 pmid:12010286
    CrossRefPubMed
  88. 88.
    1. Alvarez-Linera J,
    2. Benito-León J,
    3. Escribano J, et al
    . Prospective evaluation of carotid artery stenosis: elliptic centric contrast-enhanced MR angiography and spiral CT angiography compared with digital subtraction angiography. AJNR Am J Neuroradiol 2003;24:1012–19 pmid:12748115
    Abstract/FREE Full Text
  89. 89.
    1. Lv P,
    2. Lin J,
    3. Guo D, et al
    . Detection of carotid artery stenosis: a comparison between 2 unenhanced MRAs and dual-source CTA. AJNR Am J Neuroradiol 2014;35:2360–65 doi:10.3174/ajnr.A4073 pmid:25104291
    Abstract/FREE Full Text
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J. Yuan, A. Usman, T. Das, A.J. Patterson, J.H. Gillard, M.J. Graves
Imaging Carotid Atherosclerosis Plaque Ulceration: Comparison of Advanced Imaging Modalities and Recent Developments
American Journal of Neuroradiology Apr 2017, 38 (4) 664-671; DOI: 10.3174/ajnr.A5026

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Imaging Carotid Atherosclerosis Plaque Ulceration: Comparison of Advanced Imaging Modalities and Recent Developments
J. Yuan, A. Usman, T. Das, A.J. Patterson, J.H. Gillard, M.J. Graves
American Journal of Neuroradiology Apr 2017, 38 (4) 664-671; DOI: 10.3174/ajnr.A5026
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