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AJR 2005; 185:772-783
© American Roentgen Ray Society


Pictorial Essay

CT Neuroangiography: A Glance at the Common Pitfalls and Their Prevention

Deepak Takhtani1

1 Department of Radiology, Johns Hopkins School of Medicine, B100G Phipps Basement, 600 N. Wolfe St., Baltimore, MD 21287.

Received September 21, 2004; accepted after revision November 11, 2004.

 
Address correspondence to D. Takhtani (dtakhta1{at}jhmi.edu).


Abstract
Top
Abstract
Introduction
Possible Pitfalls
Technical Factors
References
 
OBJECTIVE. The author's objective was to address several pitfalls and missteps of CT angiography (CTA) with pictorial examples and ways to overcome potential misinterpretations. CTA is increasingly used for the noninvasive evaluation of the carotid and intracranial vessels. Ease of data acquisition may belie the complexity of interpreting each individual vessel and understanding myriad postprocessing techniques, each with its strengths and weaknesses.

CONCLUSION. Diagnostic yield and accuracy of CT angiography are enhanced by good data acquisition and by understanding and fully exploiting postprocessing techniques.


Introduction
Top
Abstract
Introduction
Possible Pitfalls
Technical Factors
References
 
Newer-generation MDCT scanners with submillimeter detectors and subsecond rotation capabilities have led to quantum leaps in the noninvasive evaluation of the cerebral vasculature. Some of the MDCTs have isotropic voxel capability that ensures the same resolution in every plane of reformations. CT angiography (CTA) has been shown to be equal if not better than conventional angiogram in the detection of cerebral aneurysms [1]. In a series of 41 aneurysms measuring equal to or less than 4 mm, sensitivity of CTA for the detection of cerebral aneurysms was higher than that of digital subtraction angiography, with equal specificity [2]. In another study, aneurysms that were overlooked at the initial interpretation of CTA were identified at a retrospective reading [3]. This underscores the importance of careful scrutiny of CTA and the need to be familiar with factors that can adversely affect the interpretation. Several pitfalls of CTA have been described, including difficulty in visualization of small arteries, differentiating the infundibular dilatation at the origin of an artery from an aneurysm, venous structures that can simulate or hide aneurysms, and an inability to identify thrombosis and calcification on 3D images [4]. CTA is better performed with automated trigger capability to optimize the contrast bolus.



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Fig. 1A Right arm versus left arm injection. Right arm injection. Contrast material in brachiocephalic vein steers clear of origin of major arteries.

 



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Fig. 1B Right arm versus left arm injection. Contrast material is in left brachiocephalic vein arching over major arteries, which can produce streak artifacts and obscure origin of major vessels.

 
CTA is also useful in diagnosing carotid stenosis and has more than a 90% concordance rate with conventional angiogram [5]. Plaques and ulcerations are better visualized on the CTA than digital subtraction angiography [6]. Accuracy of CTA depends on many factors, including the use of proper reconstruction thickness, choosing the appropriate postprocessing technique, perusal of the source data, and suitable windowing. Postprocessing techniques such as maximum intensity projection (MIP), volume rendering, and multiplanar reformation (MPR) have strengths and weaknesses. In this pictorial essay, illustrations of pitfalls resulting from technical factors or postprocessing methods and ways to avoid these are presented.



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Fig. 2A Effect of reconstruction slice thickness. Volume-rendered image with 2-mm slice reconstruction. Arrow = pseudostenosis.

 



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Fig. 2B Effect of reconstruction slice thickness. 1-mm reconstruction from same raw data set. Note pseudostenosis and diffusely attenuated arteries in A, which improve in this image.

 



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Fig. 3A Stair-step or zebra-stripe artifact. 3D volume-rendered image from 1-mm slices with 1.5-mm gap reconstruction parameters shows zebralike appearance of bone and some attenuation of middle cerebral artery branches (arrow).

 



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Fig. 3B Stair-step or zebra-stripe artifact. Image was created with 1-mm slices and 0.5-mm overlap from same raw data, and provides better delineation of smaller vessels, smooth bone background, and better visualization of distal vessels. Incidental note is made of right vertebral artery stenosis (arrow).

 

Possible Pitfalls
Top
Abstract
Introduction
Possible Pitfalls
Technical Factors
References
 
Site of Injection
For the neck carotid study, it is preferable to inject from the right arm to avoid artifacts from dense contrast in the brachiocephalic vein and superior vena cava (Figs. 1A, and 1B).



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Fig. 4A Partially thrombosed aneurysm in a 52-year-old man. Actual size of aneurysm is larger on source image (A) than appreciated on 3D reconstructed images (B).

 



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Fig. 4B Partially thrombosed aneurysm in a 52-year-old man. Actual size of aneurysm is larger on source image (A) than appreciated on 3D reconstructed images (B).

 



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Fig. 5A Presumed schwannoma likely to be misinterpreted as aneurysm in a 6-year-old girl. Maximum-intensity-projection image shows an aneurysm-like structure in relation to posterior cerebral artery (arrow).

 



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Fig. 5B Presumed schwannoma likely to be misinterpreted as aneurysm in a 6-year-old girl. Volume-rendered image shows suspected aneurysm at right P1 and P2 junction (arrow).

 



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Fig. 5C Presumed schwannoma likely to be misinterpreted as aneurysm in a 6-year-old girl. Source image clearly separates lesion (arrow) from vessel and rules out aneurysm. Conventional catheter angiogram was negative.

 



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Fig. 6A Vertebral artery dissection in a 67-year-old woman. Limitation of volume-rendered technique. Volume-rendered picture of vertebral artery (A) shows alternate areas of narrowing and dilatation but fails to show intimal flap (arrow, B-D) seen on curved multiplanar reconstruction (B) and source image (C). Angiogram done later confirms finding (D).

 



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Fig. 6B Vertebral artery dissection in a 67-year-old woman. Limitation of volume-rendered technique. Volume-rendered picture of vertebral artery (A) shows alternate areas of narrowing and dilatation but fails to show intimal flap (arrow, B-D) seen on curved multiplanar reconstruction (B) and source image (C). Angiogram done later confirms finding (D).

 



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Fig. 6C Vertebral artery dissection in a 67-year-old woman. Limitation of volume-rendered technique. Volume-rendered picture of vertebral artery (A) shows alternate areas of narrowing and dilatation but fails to show intimal flap (arrow, B-D) seen on curved multiplanar reconstruction (B) and source image (C). Angiogram done later confirms finding (D).

 



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Fig. 6D Vertebral artery dissection in a 67-year-old woman. Limitation of volume-rendered technique. Volume-rendered picture of vertebral artery (A) shows alternate areas of narrowing and dilatation but fails to show intimal flap (arrow, B-D) seen on curved multiplanar reconstruction (B) and source image (C). Angiogram done later confirms finding (D).

 



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Fig. 7A Follow-up in 54-year-old man with stents placed in the transverse and sigmoid sinuses for the thrombosis. Volume rendering versus curved multiplanar reformations. 3D volume-rendered image of right transverse and sigmoid sinuses does not reveal information about its lumen or wall.

 



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Fig. 7B Follow-up in 54-year-old man with stents placed in the transverse and sigmoid sinuses for the thrombosis. Volume rendering versus curved multiplanar reformations. Curved multiplanar reconstruction through same shows stent and areas of thrombus formation (arrow) in transverse and sigmoid venous sinuses.

 



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Fig. 8A Maximum intensity projection (MIP) of circle of Willis. MIP with 10-mm slab in axial plane (A) suggests that middle (arrow) and posterior cerebral arteries (arrowhead) are occluded; however, 40-mm MIP slab reformation (B) shows full extent of arteries. Veins are also visualized. Internal cerebral veins are seen (arrow).

 



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Fig. 8B Maximum intensity projection (MIP) of circle of Willis. MIP with 10-mm slab in axial plane (A) suggests that middle (arrow) and posterior cerebral arteries (arrowhead) are occluded; however, 40-mm MIP slab reformation (B) shows full extent of arteries. Veins are also visualized. Internal cerebral veins are seen (arrow).

 



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Fig. 9A 73-year-old woman with history of transient ischemic attack. Curved multiplanar reconstruction image of carotid shows true lumen of internal carotid with calcific plaques in arterial wall.

 



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Fig. 9B 73-year-old woman with history of transient ischemic attack. Volume-rendered 3D image fails to shows extent of stenosis, as it incorporates calcified plaques in image and surface of artery appears blistered (arrow).

 

Technical Factors
Top
Abstract
Introduction
Possible Pitfalls
Technical Factors
References
 
Reconstruction Slice Thickness and Slice Overlap
Raw data acquired during the scanning can be manipulated to get the desired slice thickness and overlap. It is not possible to get a smaller slice thickness than the detector collimation. For example, if the selected detector collimation is 1.0 mm, one cannot reconstruct at 0.5 mm. However, it is possible to reconstruct a thicker slice. Thickness of the reconstructed slices has bearing on the quality of the 3D reconstructions (Figs. 2A, and 2B). Overlapping the reconstructed slices is important to minimize the stair-step artifact. We usually acquire reconstructed slices with 30-50% overlap. Slices with no overlap or interslice gaps compromise the 3D processing and introduce artifacts and false stenosis (Figs. 3A, and 3B).

Source Images
Source images should be reviewed in all cases, irrespective of the clinical indication. As the reconstruction is done using the data from the source images, any finding seen on the processed image should be present on the source images. It is important to look for discordance between the reconstructed images and the source images (Figs. 4A, and 4B). Source images are also critical when a brightly enhancing lesion is located close to a high-probability aneurysm site. Such strategically located enhancing lesions like meningioma or schwannoma can mimic an aneurysm (Figs. 5A, 5B, and 5C). We also rely on the source images to review the vessels in areas such as the base of skull, where sculpting and 3D techniques are difficult.

Postprocessing Techniques
There are three main postprocessing techniques for CTA: MPR, MIP, and volume rendering. MPR can be in a straight, oblique, or curved oblique plane. Since the carotids have a twisted course, curved MPR capability is helpful. Curved MPRs are also helpful in the cavernous segment of the internal carotid artery (ICA), a relatively difficult area to evaluate on CTA. MPR reconstruction can be one or more than one pixel thick and is equivalent to taking a slice through the artery. Many vendors provide automated or semiautomated curved multiplanar reconstruction capability in which the vessel is traced based on the Hounsfield units (H). The automated tracing may not work consistently as the tracer can wander off along the closely lying contrast-filled veins and high-density bone. The author finds manual tracing of the vessels reliable, although it takes a few extra minutes. MPRs provide the luminal and intraluminal information better than MIP and volume-rendering techniques, as it is akin to taking thin sequential slices through the vessel. However, it is important to get MPRs in at least two planes to get more accurate information. MPR is particularly useful in areas of stenosis, visualization of the intimal flap in dissection, plaques, and intraluminal defects (Figs. 6A, 6B, 6C, 6D, 7A, and 7B).

The MIP technique involves selection of the brightest pixels to make the image while discarding the rest. MIP provides a 2D or 3D view of the structures on CTA. We have found MIP useful in intracranial vessels and in areas in which calcified plaques are present. Unlike volume rendering, MIP does not provide "depth" in an image and the structures appear overlapped or pruned. This has the potential to provide misleading information (Figs. 8A, and 8B). One could vary the width of the MIP slab to match the vessel diameter and avoid overlapping of vessels. MIP shows the calcification and stenosis better than volume-rendered images.

The volume-rendering technique uses all the pixels and thus provides a real 3D look. However, with this technique, it is not possible to look into the lumen and discriminate calcium from the wall or the lumen (Figs. 9A, and 9B). Calcific plaques in the wall give the appearance of "blisters" on the volume-rendered images and sometimes resemble aneurysm (Figs. 10A, and 10B). The volume-rendered technique is good for intracranial vessels, such as the middle and anterior cerebral arteries in which calcifications are less likely and with their location away from the bone.



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Fig. 10A 57-year-old man with headaches. Calcific plaque on source image (arrow) (A) masquerades as aneurysm (arrow) on volume-rendered 3D image (B).

 


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Fig. 10B 57-year-old man with headaches. Calcific plaque on source image (arrow) (A) masquerades as aneurysm (arrow) on volume-rendered 3D image (B).

 



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Fig. 11A 75-year-old man with transient ischemic attack. Images show importance of appropriate windowing. 3D volume-rendered image on right with width and center of 200/180 H shows diffusely attenuated vessels.

 



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Fig. 11B 75-year-old man with transient ischemic attack. Images show importance of appropriate windowing. Width/center of 200/140 H shows many more peripheral branches and no significant stenosis.

 
Windowing
"Tuning" the windows provides better contrast between two adjacent structures. In the volume-rendering technique, inappropriate window settings can create pseudostenosis, making the lesion disappear or the vessels pruned (Figs. 11A, and 11B). A very clear background may be one indication that windowing is too wide. One should alter the window center or level so that the background begins to turn a little "dirty," or the vessels stop increasing in caliber. In our experience, a window width of 200-250 H and center/level of 140-180 H is optimum. In case of less contrast in the vessels, the center of the window may need to be lowered.



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Fig. 12A 47-year-old man with subarachnoid hemorrhage.Venous confluence masks an aneurysm. Veins obscure aneurysm (arrow) in proximal left A1 segment.

 



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Fig. 12B 47-year-old man with subarachnoid hemorrhage.Venous confluence masks an aneurysm. After clearing overlying venous branches, aneurysm (arrow) is clearly visualized.

 



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Fig. 12C 47-year-old man with subarachnoid hemorrhage.Venous confluence masks an aneurysm. Aneurysm (arrow) was confirmed on angiogram.

 



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Fig. 13A 53-year-old woman with headaches. Venous confluence at internal carotid artery (ICA) terminus. Confluence of veins at ICA terminus (arrow) on source image (A) gives appearance of aneurysm (arrow) on volume-rendered image (B).

 



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Fig. 13B 53-year-old woman with headaches. Venous confluence at internal carotid artery (ICA) terminus. Confluence of veins at ICA terminus (arrow) on source image (A) gives appearance of aneurysm (arrow) on volume-rendered image (B).

 



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Fig. 13C 53-year-old woman with headaches. Venous confluence at internal carotid artery (ICA) terminus. MR angiogram is normal.

 



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Fig. 14A Pseudofenestration in 76-year-old woman with history of right-sided weakness. 3D time-of-flight MR angiography shows stenosis of right M1 segment (arrow).

 



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Fig. 14B Pseudofenestration in 76-year-old woman with history of right-sided weakness. Volume-rendered image on CT angiography shows pseudofenestration due to deep middle cerebral vein (curved arrow) running parallel to stenosed middle cerebral artery (straight arrow). Basal vein of Rosenthal and posterior communicating artery are superimposed (arrowhead).

 
Venous Structures
Opacification of the venous structures is inevitable on CTA, as the circulation time from the arteries to veins is just 3-6 sec. Wetzel et al. [7] report that the sensitivity of CT venography in defining the cerebral veins is comparable with digital subtraction angiography. To avoid misinterpretation from simultaneous opacification, venous structures should be differentiated from arteries by understanding the anatomy of some common veins. One such vein, the basal vein of Rosenthal gets its tributaries from the deep middle cerebral, olfactory, front-orbital, anterior-cerebral and inferior-striate veins [8]. Some of its tributaries converge on the ICA terminus and proximal M1 and A1 segments, causing "kissing artifacts." The vein also follows a path parallel to the posterior communicating artery and may be mistaken for it. One should try to trace the vessels to their tributaries or branches on the source images to differentiate venous from arterial structures. Tributaries to the basal vein of Rosenthal may be mistaken for, obscure, or resemble an aneurysm in the region of the ICA terminus or M1 segment of the MCA (Figs. 12A, 12B, and 12C).



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Fig. 14C Pseudofenestration in 76-year-old woman with history of right-sided weakness. Maximum-intensity-projection image shows same finding. Mild difference in density of contrast between vein (curved arrow) and artery (straight arrow) is evident.

 



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Fig. 15A 70-year-old man with ataxia. Basilar artery stenosis is hidden by pontomesencephalic vein. Normal variant vein (arrow) obscures basilar artery stenosis.

 



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Fig. 15B 70-year-old man with ataxia. Basilar artery stenosis is hidden by pontomesencephalic vein. Rotation of image shows relationship of vein (small arrow) and stenosis in basilar artery (thick arrow).

 
The confluence of venous tributaries near the ICA terminus may look like an aneurysm (Figs. 13A, 13B, and 13C). Rarely, an artery and vein lying close to each other may be mistaken for fenestration (Figs. 14A, 14B, and 14C). Aberrant veins may also be mistaken for a normal vessel concealing the artery [9] (Figs. 15A, and 15B).



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Fig. 16 51-year-old woman with headaches. Source axial image shows small aneurysm (thin arrow) by side of posterior communicating artery (thick arrow).

 



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Fig. 17A CT angiography on 81-year-old man for evaluation of carotid stenosis. Pseudothrombus in jugular veins. Reflux of contrast into jugular veins mimics thrombi.

 



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Fig. 17B CT angiography on 81-year-old man for evaluation of carotid stenosis. Pseudothrombus in jugular veins. Sagittal reformation and axial images show contrast material localized in dependent posterior aspect of veins. Sagittal reformation (B) also shows continuous column of contrast material extending from brachiocephalic to jugular vein.

 



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Fig. 17C CT angiography on 81-year-old man for evaluation of carotid stenosis. Pseudothrombus in jugular veins. Sagittal reformation and axial images show contrast material localized in dependent posterior aspect of veins. Sagittal reformation (B) also shows continuous column of contrast material extending from brachiocephalic to jugular vein.

 
Infundibulum Versus Aneurysm
At times it may be difficult to differentiate an infundibulum from a small aneurysm, such as in cases where the branch arising from the tip is beyond the resolution of the CTA. This is especially true if the lumen of the vessel is less than 0.5 mm. Decreasing the window center on volume-rendered images may help visualize a faintly opacified vessel at the tip of the aneurysm. In some cases, careful review of the source images may be of help to differentiate an aneurysm from the adjacent normal artery (Fig. 16).

Venous Reflux
In some patients, contrast may reflux back into the jugular veins and other neck veins and mix with noncontrasted blood to give an appearance of a filling defect, suggesting a thrombus (Figs. 17A, 17B, and 17C).


References
Top
Abstract
Introduction
Possible Pitfalls
Technical Factors
References
 

  1. Karamessini MT, Kagadis GC, Petsas T, et al. CT angiography with three-dimensional techniques for the early diagnosis of intracranial aneurysms. Comparison with intra-arterial DSA and the surgical findings. Eur J Radiol 2004;49 : 212-223[CrossRef][Medline]
  2. Villablanca JP, Jahan R, Hooshi P, et al. Detection and characterization of very small cerebral aneurysms by using 2D and 3D helical CT angiography. Am J Neuroradiol 2002;23 : 1187-1198[Abstract/Free Full Text]
  3. Jayaraman MV, Mayo-Smith WW, Tung GA, et al. Detection of intracranial aneurysms: multi-detector row CT angiography compared with DSA. Radiology 2004;230 : 510-518[Abstract/Free Full Text]
  4. Tomandl BF, Kostner NC, Schempershofe M, et al. CT angiography of intracranial aneurysms: a focus on postprocessing. RadioGraphics 2004;24 : 637-655[Abstract/Free Full Text]
  5. Moll R, Dinkel HP. Value of the CT angiography in the diagnosis of common carotid artery bifurcation disease: CT angiography versus digital subtraction angiography and color flow Doppler. Eur J Radiol 2001; 39:155 -162[CrossRef][Medline]
  6. Randoux B, Marro B, Koskas F, et al. Carotid artery stenosis: prospective comparison of CT, three-dimensional gadolinium-enhanced MR, and conventional angiography. Radiology 2001;220 : 179-185[Abstract/Free Full Text]
  7. Wetzel SG, Kirsch E, Stock KW, Kolbe M, Kaim A, Raude EW. Cerebral veins: comparative study of CT venography with intraarterial digital subtraction angiography. Am J Neuroradiol1999; 20:249 -255[Abstract/Free Full Text]
  8. Suzuki Y, Ikeda H, Shimadu M, Ikeda Y, Matsumoto K. Variations of the basal vein: identification using three-dimensional CT angiography. Am J Neuroradiol 2001;l22 : 670-676[Abstract/Free Full Text]
  9. Teksam M, Casey S, McKinney A, Michel E, Truwit CL. Anatomy and frequency of large pontomesencephalic veins on 3D CT angiograms of the circle of Willis. Am J Neuroradiol 2003;24 : 1598-1601[Abstract/Free Full Text]

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